Team:SYSU-Software/Models
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- | <a href="/" class="sysu-title"></a> | + | <a href="https://2012.igem.org/Team:SYSU-Software" class="sysu-title"></a> |
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- | <li class="mainlevel" id="mainlevel_01"><a href="https://2012.igem.org/Team:SYSU-Software | + | <li class="mainlevel" id="mainlevel_01"><a href="https://2012.igem.org/Team:SYSU-Software"> Home</a> |
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<li class="mainlevel"><a href="https://2012.igem.org/Team:SYSU-Software/Notebook">Notebook</a></li> | <li class="mainlevel"><a href="https://2012.igem.org/Team:SYSU-Software/Notebook">Notebook</a></li> | ||
+ | <li class="mainlevel"><a href="https://2012.igem.org/Team:SYSU-Software/Practice"> | ||
+ | Tips</a><!--input an em tag as a space,IE is gread need--> | ||
+ | </li> | ||
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<div id="content"> <div class="entry page clear"> | <div id="content"> <div class="entry page clear"> | ||
- | <h1 id="doctitle" class="pagetitle">Models | + | <h1 id="doctitle" class="pagetitle" style="line-height: 1.5em;"> |
- | <h1 id=" | + | Algorithm&Models</h1> |
- | </span> | + | <table class="doc-toc"> |
- | + | <tbody> | |
- | <p> </p> | + | <tr> |
- | <h1 id=" | + | <td> |
- | + | <div id="toctitle"> | |
- | < | + | <h2>Contents</h2> |
- | </div> | + | </div> |
+ | <ul id="toc-ul"> | ||
+ | <li class="toclevel-1"><a href="#pp1"> <span class="toctext"> Flux Balance Analysis </span></a></li> | ||
+ | <li class="toclevel-1"><a href="#pp2">SiRNA designer</a></li> | ||
+ | <li class="toclevel-1"><a href="#pp3">Riboswitch designer</a></li> | ||
+ | |||
+ | </ul> | ||
+ | </td> | ||
+ | </tr> | ||
+ | </tbody> | ||
+ | </table> | ||
+ | |||
+ | <div id="doc-contents"> | ||
+ | <div> | ||
+ | <h1 id="pp1">Flux Balance Analysis</h1> | ||
+ | <p> Traditional approaches for metabolic network exploration are mainly based on physicochemical kinetics laws and principles. However,the difficulty for monitoring nutritional changes in metabolic biosystem neccecitates a more reductionist form of information especially available for computational processing. In 1992, Savinell and Palsson[1,2]proposed flux balance analysis(FBA) to simulate microbial metabolism and in 1993 FBA was applied in exploration of E.coli System[3,4,5].Thereafer, Palsson and his parters extend the uses of FBA even to genetic level[6,7].</p> | ||
+ | </div> | ||
+ | <div> | ||
+ | <p > Here are the mathematical description of FBA[8]. Firstly, FBA assumes that metabolic networks will reach homeostasis constrained by stoichiometry without knowing material changes all along the process. The values in this stoichiometric matrix are the stoichiometric coefficients of each reaction in the system as the set of constraints for the optimization. The mathematical description can be interpreted in the simple example with graphs following.</p> | ||
+ | <p ><img src="https://static.igem.org/mediawiki/igem.org/4/4b/Image001.png" style="width: 630px;"></p> | ||
+ | </div> | ||
+ | <div> | ||
+ | <p> In the simple biosystem illustrated above, the compounds served as the nodes are connected by the reactions for conversion among compounds. The increase of Compound A is due to the converstion from Compound C and A, while the decrease of Compound A is the result of the conversion from Compound A to C. The graph below shows the overall change of the amount per time unit of Compound A, B, C. </p> | ||
+ | <p ><img src="https://static.igem.org/mediawiki/igem.org/b/b2/Image004.jpg" ></p> | ||
+ | |||
+ | <p> Since the whole system will reach homeostasis, which means a state that compound in the system will be constant, in other words, the flux-in and flux-out of the node(the compound) will be equal. That is why we call this method ‘Flux Balance Analysis’.</p> | ||
+ | <p ><img src="https://static.igem.org/mediawiki/igem.org/e/e9/Image006.jpg" ></p> | ||
+ | <p> Secondly, the results above can be translated into a stoichiometric matrix. In Matrix S below.</p> | ||
+ | <p ><img src="https://static.igem.org/mediawiki/igem.org/2/21/Image007.jpg" ></p> | ||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
+ | <p> Each col of Matrix S represents stoichiometric coefficients the related to each compound and each row of Matrix S refers to coefficients of each reaction according to the three equations above. The plus and minus signs are determined by the direction of reations according to the compound itself.</p> | ||
+ | <p ><img src="https://static.igem.org/mediawiki/igem.org/8/82/Image010.jpg" ></p> | ||
+ | <p> While in the vector above, v1 and v2 represents the reaction rate namely fluxes of the two reactions in this sample system.</p> | ||
+ | <p>So you can see the multiplication of Matrix S and the vector can return to those three original equations above. As has been explained, the multiplication will be the zero vector.</p> | ||
+ | <p ><img src="https://static.igem.org/mediawiki/igem.org/7/70/Image012.jpg" ></p> | ||
+ | <p> In the general case we can write:</p> | ||
+ | <p > | ||
+ | <img src="https://static.igem.org/mediawiki/igem.org/2/26/Image013.jpg" width="108" height="42" ></p><p> Thirdly,with stoichiometry prepared and the objective function(the biomass function) determined, linear programming can be performed for optimization.</p> | ||
+ | <p > <img src="https://static.igem.org/mediawiki/igem.org/3/3d/Image015.jpg" ></p><p> In many cases, constraints are set upon the values of fluxes based on some thermodynamic conditions.</p> | ||
+ | <p > <img src="https://static.igem.org/mediawiki/igem.org/a/a1/Image017.jpg" ></p> | ||
+ | <p class="MsoNormal"><span lang="EN-US" style="mso-no-proof:yes">(All the graphs | ||
+ | are from Wikipedia.)<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="font-family:"Times New Roman","serif"; | ||
+ | mso-no-proof:yes">Reference:<o:p></o:p></span></p> | ||
+ | <p> 1.Savinell JM, Palsson BO: Optimal selection of metabolic fluxes for in vivo measurement. I. Development of mathematical methods. J Theor Biol 1992, 155:201-214.</p> | ||
+ | <p>2. Savinell JM, Palsson BO: Optimal selection of metabolic fluxes for in vivo measurement. II. Application to Escherichia coli and hybridoma cell metabolism. J Theor Biol 1992,155:215-242.</p> | ||
+ | <p>3.Varma A, Palsson BO: Metabolic capabilities of Escherichia coli:I. Synthesis of biosynthetic precursors and cofactors. J TheorBiol 1993, 165:477-502.</p> | ||
+ | <p>4. Varma A, Palsson BO: Metabolic capabilities of Escherichia coli:II. Optimal growth patterns. J Theor Biol 1993,165:503-522.</p> | ||
+ | <p>5. Varma A, Palsson BO: Stoichiometric flux balance models quantitatively predict growth and metabolic by-product secretion in wild-type Escherichia coli W3110. Appl Environ Microbiol 1994, 60:3724-3731.</p> | ||
+ | <p>6. Edwards JS, Palsson BO: The Escherichia coli MG1655 in silico metabolic genotype: its definition, characteristics, and capabilities. Proc Natl Acad Sci USA 2000, 97:5528-5533.</p> | ||
+ | <p>7.Edwards JS, Palsson BO: Robustness analysis of the Escherichia coli metabolic network. Biotechnol Prog 2000, 16:927-939.</p> | ||
+ | <p>8. Kenneth J Kauffman, Purusharth Prakash and Jeremy S Edwards: Advances in flux balance analysis, Current Opinion in Biotechnology 2003, 14:491–496</p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | <h1 id="pp2">SiRNA designer</h1> | ||
+ | |||
+ | <h3><span lang="EN-US" style="background: white">Tom Tuschl's rule (for | ||
+ | cDNA)<o:p></o:p></span></h3> | ||
+ | <p class="MsoNormal"><span lang="EN-US">1. Select targeted region from a | ||
+ | given cDNA sequence beginning 50-100 nt downstream of start codon<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"><span lang="EN-US">2. Look for sequence motif | ||
+ | AA+N19+TT first. If there is no suitable sequence look 23-nt sequence | ||
+ | motif NA+N21 and convert the 3' end of the sense siRNA to TT<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"><span lang="EN-US">3. Or search for NAR+N17+YNN<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"><span lang="EN-US">PS: Target sequence should have | ||
+ | a GC content of around 50%<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"><span lang="EN-US">R means A/G, and Y means T/C.<o:p></o:p></span></p> | ||
+ | <h3><span lang="EN-US" style="background: white">Rational siRNA | ||
+ | design(for mRNA)<o:p></o:p></span></h3> | ||
+ | <p class="MsoNormal"><span lang="EN-US">Evaluate potential candidates | ||
+ | and assign scores to them, sequences with higher scores will have higher | ||
+ | chance of success in RNAi. <o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"><span lang="EN-US">The table below lists the 8 | ||
+ | criteria and the methods of score assignment.<o:p></o:p></span></p> | ||
+ | <table class="MsoNormalTable" border="1" cellspacing="0" cellpadding="0" width="708" style="width:425.0pt;border-collapse:collapse;border:none;mso-border-top-alt: | ||
+ | solid windowtext .5pt;mso-border-bottom-alt:solid windowtext .5pt;mso-yfti-tbllook: | ||
+ | 1184;mso-padding-alt:0cm 5.4pt 0cm 5.4pt;mso-border-insideh:.5pt solid windowtext"> | ||
+ | <tr style="mso-yfti-irow:0;mso-yfti-firstrow:yes"> | ||
+ | <td width="72" rowspan="2" style="width:42.9pt;border-top:solid windowtext 1.0pt; | ||
+ | border-left:none;border-bottom:solid windowtext 1.0pt;border-right:none; | ||
+ | mso-border-top-alt:solid windowtext .5pt;mso-border-bottom-alt:solid windowtext .5pt; | ||
+ | padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal" align="center"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">Criteria<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="386" rowspan="2" style="width:231.85pt;border-top:solid windowtext 1.0pt; | ||
+ | border-left:none;border-bottom:solid windowtext 1.0pt;border-right:none; | ||
+ | mso-border-top-alt:solid windowtext .5pt;mso-border-bottom-alt:solid windowtext .5pt; | ||
+ | padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal" align="center"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">Description<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="250" colspan="2" valign="top" style="width:150.25pt;border-top:solid windowtext 1.0pt; | ||
+ | border-left:none;border-bottom:solid windowtext 1.0pt;border-right:none; | ||
+ | mso-border-top-alt:solid windowtext .5pt;mso-border-bottom-alt:solid windowtext .5pt; | ||
+ | padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal" align="center"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">Score<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr style="mso-yfti-irow:1"> | ||
+ | <td width="154" style="width:92.15pt;border:none;border-bottom:solid windowtext 1.0pt; | ||
+ | mso-border-top-alt:solid windowtext .5pt;mso-border-top-alt:solid windowtext .5pt; | ||
+ | mso-border-bottom-alt:solid windowtext .5pt;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal" align="center"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">Yes<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="97" valign="top" style="width:58.1pt;border:none;border-bottom:solid windowtext 1.0pt; | ||
+ | mso-border-top-alt:solid windowtext .5pt;mso-border-top-alt:solid windowtext .5pt; | ||
+ | mso-border-bottom-alt:solid windowtext .5pt;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal" align="center"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">No<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr style="mso-yfti-irow:2"> | ||
+ | <td width="72" valign="top" style="width:42.9pt;border:none;mso-border-top-alt: | ||
+ | solid windowtext .5pt;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">1<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="386" valign="top" style="width:231.85pt;border:none;mso-border-top-alt: | ||
+ | solid windowtext .5pt;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">Moderate to | ||
+ | low (30%-52%) GC Content<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="154" valign="top" style="width:92.15pt;border:none;mso-border-top-alt: | ||
+ | solid windowtext .5pt;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">1 point<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="97" valign="top" style="width:58.1pt;border:none;mso-border-top-alt: | ||
+ | solid windowtext .5pt;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr style="mso-yfti-irow:3"> | ||
+ | <td width="72" valign="top" style="width:42.9pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">2<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="386" valign="top" style="width:231.85pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">At least 3 | ||
+ | A/Us at positions 15-19 (sense)<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="154" valign="top" style="width:92.15pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">1 point | ||
+ | /per A or U<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="97" valign="top" style="width:58.1pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr style="mso-yfti-irow:4"> | ||
+ | <td width="72" valign="top" style="width:42.9pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">3<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="386" valign="top" style="width:231.85pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">Melting | ||
+ | temperature-Tm*<20</span><span style="mso-bidi-font-size:10.5pt; | ||
+ | font-family:宋体;mso-ascii-font-family:"Times New Roman";mso-hansi-font-family: | ||
+ | "Times New Roman"">℃</span><span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="154" valign="top" style="width:92.15pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">1 point<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="97" valign="top" style="width:58.1pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr style="mso-yfti-irow:5"> | ||
+ | <td width="72" valign="top" style="width:42.9pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">4<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="386" valign="top" style="width:231.85pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">A at | ||
+ | position 19 (sense)<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="154" valign="top" style="width:92.15pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">1 point<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="97" valign="top" style="width:58.1pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr style="mso-yfti-irow:6"> | ||
+ | <td width="72" valign="top" style="width:42.9pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">5<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="386" valign="top" style="width:231.85pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">A at | ||
+ | position 3 (sense)<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="154" valign="top" style="width:92.15pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">1 point<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="97" valign="top" style="width:58.1pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr style="mso-yfti-irow:7"> | ||
+ | <td width="72" valign="top" style="width:42.9pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">6<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="386" valign="top" style="width:231.85pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">U at | ||
+ | position 10 (sense)<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="154" valign="top" style="width:92.15pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">1 point<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="97" valign="top" style="width:58.1pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr style="mso-yfti-irow:8"> | ||
+ | <td width="72" valign="top" style="width:42.9pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">7<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="386" valign="top" style="width:231.85pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">No G/C at | ||
+ | position 19 (sense)<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="154" valign="top" style="width:92.15pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | </td> | ||
+ | <td width="97" valign="top" style="width:58.1pt;border:none;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">-1 point<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr style="mso-yfti-irow:9;mso-yfti-lastrow:yes"> | ||
+ | <td width="72" valign="top" style="width:42.9pt;border:none;border-bottom:solid windowtext 1.0pt; | ||
+ | mso-border-bottom-alt:solid windowtext .5pt;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">8<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="386" valign="top" style="width:231.85pt;border:none;border-bottom: | ||
+ | solid windowtext 1.0pt;mso-border-bottom-alt:solid windowtext .5pt; | ||
+ | padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">No G at | ||
+ | position 13 (sense)<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td width="154" valign="top" style="width:92.15pt;border:none;border-bottom:solid windowtext 1.0pt; | ||
+ | mso-border-bottom-alt:solid windowtext .5pt;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | </td> | ||
+ | <td width="97" valign="top" style="width:58.1pt;border:none;border-bottom:solid windowtext 1.0pt; | ||
+ | mso-border-bottom-alt:solid windowtext .5pt;padding:0cm 5.4pt 0cm 5.4pt"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">-1 point<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">The "anti-sense" | ||
+ | strand is the siRNA strand that is complementary to the target mRNA and | ||
+ | that will be binding to the mRNA.<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">The melting | ||
+ | temperature’ of a siRNA candidate can be calculated by the formula | ||
+ | showed below:<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <o:p></o:p> | ||
+ | <img class="decoded" alt="https://static.igem.org/mediawiki/igem.org/e/e8/Image101.png" src="https://static.igem.org/mediawiki/igem.org/e/e8/Image101.png"></p> | ||
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+ | <v:imagedata src="file:///I:\msohtmlclip1\01\clip_image001.png" o:title="" | ||
+ | chromakey="white"/> | ||
+ | </v:shape></span><span lang="EN-US" style="font-size:14.0pt"><o:p></o:p></span> | ||
+ | </p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">wA, xT, yG, zC are | ||
+ | separately the number of A, T, G, C in a siRNA candidate.<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="font-size: 10.0pt; font-family: "Arial","sans-serif"; color: black; background: white"> | ||
+ | All siRNA candidates scored higher than 6 are acceptable.</span><span lang="EN-US" style="font-size:15.0pt"><o:p></o:p></span></p> | ||
+ | <span lang="EN-US" style="font-size:10.5pt;font-family:"Times New Roman","serif"; | ||
+ | mso-fareast-font-family:宋体;mso-font-kerning:1.0pt;mso-ansi-language:EN-US; | ||
+ | mso-fareast-language:ZH-CN;mso-bidi-language:AR-SA"> | ||
+ | <br clear="all" style="mso-special-character:line-break;page-break-before:always"> | ||
+ | </span> | ||
+ | <p class="MsoNormal" align="left"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | <h1 id="pp3"><span lang="EN-US">Riboswitch designer:<o:p></o:p></span></h1> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">The designer is | ||
+ | based on a special promoter working in eukaryotes - internal ribosome | ||
+ | entry site (IRES). We design the upstream sequence that can bind to IRES | ||
+ | part so the second structure of IRES can be transformed by the ligand.<o:p></o:p></span></p> | ||
+ | <h3><span lang="EN-US">Up regulated:<o:p></o:p></span></h3> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">Target sequence is | ||
+ | assembled by five parts: MS-SL, aaIRES (anti-anti-IRES), aptamer, aIRES | ||
+ | (anti-IRES), IRES.<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <o:p></o:p> | ||
+ | <img class="decoded" style="cursor: -moz-zoom-out" alt="https://static.igem.org/mediawiki/igem.org/e/ec/Image002.png" src="https://static.igem.org/mediawiki/igem.org/e/ec/Image002.png"></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt; | ||
+ | mso-no-proof:yes"><v:shape id="图片_x0020_1" o:spid="_x0000_i1029" type="#_x0000_t75" | ||
+ | style='width:408.6pt;height:405pt;visibility:visible;mso-wrap-style:square'> | ||
+ | <v:imagedata src="file:///I:\msohtmlclip1\01\clip_image002.emz" o:title=""/> | ||
+ | </v:shape></span><span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p></o:p> | ||
+ | </span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">The IRES, aIRES, | ||
+ | aaIRES parts are settled, we get aptamer sequence according to | ||
+ | customer’s quests from aptamer database and the MS-SL is paired to the | ||
+ | combination part of aaIRES and aptamer. Then adjust the MS-SL part’s | ||
+ | length to fit it’s free energy to -11.7 kcal/mol.<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | <h3><span lang="EN-US">Down regulated:<o:p></o:p></span></h3> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">The differences | ||
+ | from down regulated to up regulated riboswitch are the order between | ||
+ | aptamer and aaIRES, the sequence of MS part. The new structure is showed | ||
+ | below:<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <o:p></o:p> | ||
+ | <img class="decoded" alt="https://static.igem.org/mediawiki/igem.org/9/90/Image003.jpg" src="https://static.igem.org/mediawiki/igem.org/9/90/Image003.jpg"></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt; | ||
+ | mso-no-proof:yes"><v:shape id="图片_x0020_4" o:spid="_x0000_i1028" type="#_x0000_t75" | ||
+ | alt="说明: C:\Users\miao\Desktop\紧急修改!!副本.jpg" style='width:414.6pt;height:211.8pt; | ||
+ | visibility:visible;mso-wrap-style:square'> | ||
+ | <v:imagedata src="file:///I:\msohtmlclip1\01\clip_image003.jpg" o:title="紧急修改!!副本"/> | ||
+ | </v:shape></span><span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p></o:p> | ||
+ | </span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">We set MS to | ||
+ | “CCUCU” under experimental data and the aptamer still comes from aptamer | ||
+ | database.<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | <h3><span lang="EN-US">Algorithm about free energy calculation comes | ||
+ | from Turner’s team:<o:p></o:p></span></h3> | ||
+ | <p class="MsoNormal"><b style="mso-bidi-font-weight:normal"> | ||
+ | <i style="mso-bidi-font-style: | ||
+ | normal"><span lang="EN-US" style="mso-bidi-font-size:10.5pt">Hairpin loops:<o:p></o:p></span></i></b></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <o:p></o:p> | ||
+ | <img class="decoded" alt="https://static.igem.org/mediawiki/igem.org/8/89/Image004.png" src="https://static.igem.org/mediawiki/igem.org/8/89/Image004.png"></p> | ||
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w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>= </m:t></m:r><m:sSub><m:sSubPr><m:ctrlPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr></m:ctrlPr></m:sSubPr><m:e><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>鈭咷掳37</m:t></m:r></m:e><m:sub><m:r><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Maciith"/><w:i/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>innition</m:t></m:r></m:sub></m:sSub><m:d><m:dPr><m:ctrlPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:i/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr></m:ctrlPr></m:dPr><m:e><m:r><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria 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+ | <v:imagedata src="file:///I:\msohtmlclip1\01\clip_image004.png" o:title="" | ||
+ | chromakey="white"/> | ||
+ | </v:shape></span><span lang="EN-US" style="font-size:14.0pt"><o:p></o:p></span> | ||
+ | </p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">In this equation, n | ||
+ | (5) is the number of nucleotides in loop, the terminal mismatch | ||
+ | parameter is the sequence-dependent term for the first mismatch stacking | ||
+ | on the terminal base pair.<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"><b style="mso-bidi-font-weight:normal"> | ||
+ | <i style="mso-bidi-font-style: | ||
+ | normal"><span lang="EN-US" style="mso-bidi-font-size:10.5pt">Watson-Crick | ||
+ | Helices:<o:p></o:p></span></i></b></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <o:p></o:p> | ||
+ | <img class="decoded" alt="https://static.igem.org/mediawiki/igem.org/3/3c/Image005.png" src="https://static.igem.org/mediawiki/igem.org/3/3c/Image005.png"></p> | ||
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wsp:val="00CC0D6A"/><wsp:rsid wsp:val="00E616C7"/><wsp:rsid wsp:val="00F65E73"/></wsp:rsids></w:docPr><w:body><wx:sect><w:p wsp:rsidR="00000000" wsp:rsidRPr="006447FA" wsp:rsidRDefault="006447FA" wsp:rsidP="006447FA"><m:oMathPara><m:oMath><m:sSub><m:sSubPr><m:ctrlPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr></m:ctrlPr></m:sSubPr><m:e><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>螖G掳37</m:t></m:r></m:e><m:sub><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>Watson-Crick</m:t><"2/m:r></m:sub></m:sSub><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>=</m:t></m:r><m:sSub><m:sSubPr><m:ctrlPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr></m:ctrlPr></m:sSubPr><m:e><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math" w:hint="fareast"/><wx:font wx:val="瀹嬩綋"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>螖</m:t></m:r><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Mathi="C"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>G掳37</m:t></m:r></m:e><m:sub><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="2C8"/></w:rPr><m:t>37 AU end penalty</m:t></m:r></m:sub></m:sSub><m:d><m:dPr><m:ctrlPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr></m:ctrlPr></m:dPr><m:e><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>per AU end</m:t></m:r></m:e></m:d><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>+</m:t></m:r><m:sSub><m:sSubPr><m:ctrlPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr></m:ctrlPr></m:sSubPr><m:e><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math" w:hint="fareast"/><wx:font wx:val="瀹嬩綋"/><th"w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>螖</m:t></m:r><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>G掳h"37</m:t></m:r></m:e><m:sub><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>37 symmetry</m:t></m:r></m:sub></m:sSub><m:d><m:dPr><m:ctrlPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr></m:ctrlPr></m:dPr><m:e><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>self-complementary duplexes</m:t></m:r></m:e></m:d><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz 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m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>G掳37</m:t></m:r></m:e><m:sub><m:r><m:rPr><m:sty m:val=/>"p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t> stacking</m:t></m:r></m:sub></m:sSub><m:r><m:rPr><m:sty m:val="p"/></m:rPr><w:rPr><w:rFonts w:ascii="Cambria Math" w:h-ansi="Cambria Math"/><wx:font wx:val="Cambria Math"/><w:sz w:val="28"/><w:sz-cs w:val="28"/></w:rPr><m:t>]</m:t></m:r></m:e></m:nary></m:oMath></m:oMathPara></w:p><w:sectPr wsp:rsidR="00000000" wsp:rsidRPr="006447FA"><w:pgSz w:w="12240" w:h="15840"/><w:pgMar w:top="1440" w:right="1800" w:bottom="1440" w:left="1800" w:header="720" w:footer="720" w:gutter="0"/><w:cols w:space="720"/></w:sectPr></wx:sect></w:body></w:wordDocument>"> | ||
+ | <v:imagedata src="file:///I:\msohtmlclip1\01\clip_image005.png" o:title="" | ||
+ | chromakey="white"/> | ||
+ | </v:shape></span> | ||
+ | <span lang="EN-US" style="font-size:14.0pt;font-family:"Cambria Math","serif""><o:p></o:p> | ||
+ | </span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">Specific data can | ||
+ | be found on web site:</span><span lang="EN-US"><o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"><span lang="EN-US"> | ||
+ | http://rna.urmc.rochester.edu/NNDB/turner04/index.html<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt"><o:p> </o:p></span></p> | ||
+ | <h2><span lang="EN-US">References:<o:p></o:p></span></h2> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">1.Elbashir SM et | ||
+ | al. (2001) Duplexes of 21-nucleotide RNAs mediate RNA interference in | ||
+ | cultured mammalian cells. Nature. 411:494-498.<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">2.Elbahir SM et al. | ||
+ | (2001). Functional anatomy of siRNAs for mediating efficient RNAi in | ||
+ | Drosophila melanogaster embryo lysate. EMBO J. 20:6877-6888.<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">3.Elbashir SM et | ||
+ | al. (2002). Analysis of gene function in somatic mammalian cells using | ||
+ | small interfering RNAs. Methods. 26:199-213.<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">4.Reynolds A, Leake | ||
+ | D, Boese Q, Scaringe S, Marshall WS, Khvorova A. Rational siRNA design | ||
+ | for RNA interference. Nat Biotechnol. 2004 Mar;22(3):326-30.<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">5.Ogawa, A. (2011). | ||
+ | Rational design of artificial riboswitches based on ligand-dependent | ||
+ | modulation of internal ribosome entry in wheat germ extract and their | ||
+ | applications as label-free biosensors. RNA (New York, N.Y.), 17(3), | ||
+ | 478-88. doi:10.1261/rna.2433111<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">6.Ogawa, A. (2012). | ||
+ | Rational construction of eukaryotic OFF-riboswitches that downregulate | ||
+ | internal ribosome entry site-mediated translation in response to their | ||
+ | ligands. Bioorganic & medicinal chemistry letters, 22(4), 1639-42. | ||
+ | Elsevier Ltd. doi:10.1016/j.bmcl.2011.12.118<o:p></o:p></span></p> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size:10.5pt">7.Turner, D. H. & | ||
+ | Mathews, D. H.<span style="mso-spacerun:yes"> </span>(2009).<span style="mso-spacerun:yes"> | ||
+ | </span>NNDB: The nearest neighbor parameter database for predicting | ||
+ | stability of nucleic acid secondary structure.<span style="mso-spacerun:yes"> | ||
+ | </span>Nucleic Acids Research.<span style="mso-spacerun:yes"> | ||
+ | </span>38, D280-D282.<o:p></o:p></span></p> | ||
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Latest revision as of 00:58, 27 September 2012
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Algorithm&Models
Contents |
Flux Balance Analysis
Traditional approaches for metabolic network exploration are mainly based on physicochemical kinetics laws and principles. However,the difficulty for monitoring nutritional changes in metabolic biosystem neccecitates a more reductionist form of information especially available for computational processing. In 1992, Savinell and Palsson[1,2]proposed flux balance analysis(FBA) to simulate microbial metabolism and in 1993 FBA was applied in exploration of E.coli System[3,4,5].Thereafer, Palsson and his parters extend the uses of FBA even to genetic level[6,7].
Here are the mathematical description of FBA[8]. Firstly, FBA assumes that metabolic networks will reach homeostasis constrained by stoichiometry without knowing material changes all along the process. The values in this stoichiometric matrix are the stoichiometric coefficients of each reaction in the system as the set of constraints for the optimization. The mathematical description can be interpreted in the simple example with graphs following.
In the simple biosystem illustrated above, the compounds served as the nodes are connected by the reactions for conversion among compounds. The increase of Compound A is due to the converstion from Compound C and A, while the decrease of Compound A is the result of the conversion from Compound A to C. The graph below shows the overall change of the amount per time unit of Compound A, B, C.
Since the whole system will reach homeostasis, which means a state that compound in the system will be constant, in other words, the flux-in and flux-out of the node(the compound) will be equal. That is why we call this method ‘Flux Balance Analysis’.
Secondly, the results above can be translated into a stoichiometric matrix. In Matrix S below.
Each col of Matrix S represents stoichiometric coefficients the related to each compound and each row of Matrix S refers to coefficients of each reaction according to the three equations above. The plus and minus signs are determined by the direction of reations according to the compound itself.
While in the vector above, v1 and v2 represents the reaction rate namely fluxes of the two reactions in this sample system.
So you can see the multiplication of Matrix S and the vector can return to those three original equations above. As has been explained, the multiplication will be the zero vector.
In the general case we can write:
Thirdly,with stoichiometry prepared and the objective function(the biomass function) determined, linear programming can be performed for optimization.
In many cases, constraints are set upon the values of fluxes based on some thermodynamic conditions.
(All the graphs
are from Wikipedia.)
Reference:
1.Savinell JM, Palsson BO: Optimal selection of metabolic fluxes for in vivo measurement. I. Development of mathematical methods. J Theor Biol 1992, 155:201-214.
2. Savinell JM, Palsson BO: Optimal selection of metabolic fluxes for in vivo measurement. II. Application to Escherichia coli and hybridoma cell metabolism. J Theor Biol 1992,155:215-242.
3.Varma A, Palsson BO: Metabolic capabilities of Escherichia coli:I. Synthesis of biosynthetic precursors and cofactors. J TheorBiol 1993, 165:477-502.
4. Varma A, Palsson BO: Metabolic capabilities of Escherichia coli:II. Optimal growth patterns. J Theor Biol 1993,165:503-522.
5. Varma A, Palsson BO: Stoichiometric flux balance models quantitatively predict growth and metabolic by-product secretion in wild-type Escherichia coli W3110. Appl Environ Microbiol 1994, 60:3724-3731.
6. Edwards JS, Palsson BO: The Escherichia coli MG1655 in silico metabolic genotype: its definition, characteristics, and capabilities. Proc Natl Acad Sci USA 2000, 97:5528-5533.
7.Edwards JS, Palsson BO: Robustness analysis of the Escherichia coli metabolic network. Biotechnol Prog 2000, 16:927-939.
8. Kenneth J Kauffman, Purusharth Prakash and Jeremy S Edwards: Advances in flux balance analysis, Current Opinion in Biotechnology 2003, 14:491–496
SiRNA designer
Tom Tuschl's rule (for
cDNA)
1. Select targeted region from a
given cDNA sequence beginning 50-100 nt downstream of start codon
2. Look for sequence motif
AA+N19+TT first. If there is no suitable sequence look 23-nt sequence
motif NA+N21 and convert the 3' end of the sense siRNA to TT
3. Or search for NAR+N17+YNN
PS: Target sequence should have
a GC content of around 50%
R means A/G, and Y means T/C.
Rational siRNA
design(for mRNA)
Evaluate potential candidates
and assign scores to them, sequences with higher scores will have higher
chance of success in RNAi.
The table below lists the 8
criteria and the methods of score assignment.
Criteria |
Description |
Score |
|
Yes |
No |
||
1 |
Moderate to
low (30%-52%) GC Content |
1 point |
|
2 |
At least 3
A/Us at positions 15-19 (sense) |
1 point
/per A or U |
|
3 |
Melting
temperature-Tm*<20℃ |
1 point |
|
4 |
A at
position 19 (sense) |
1 point |
|
5 |
A at
position 3 (sense) |
1 point |
|
6 |
U at
position 10 (sense) |
1 point |
|
7 |
No G/C at
position 19 (sense) |
|
-1 point |
8 |
No G at
position 13 (sense) |
|
-1 point |
The "anti-sense"
strand is the siRNA strand that is complementary to the target mRNA and
that will be binding to the mRNA.
The melting
temperature’ of a siRNA candidate can be calculated by the formula
showed below:
wA, xT, yG, zC are
separately the number of A, T, G, C in a siRNA candidate.
All siRNA candidates scored higher than 6 are acceptable.
Riboswitch designer:
The designer is
based on a special promoter working in eukaryotes - internal ribosome
entry site (IRES). We design the upstream sequence that can bind to IRES
part so the second structure of IRES can be transformed by the ligand.
Up regulated:
Target sequence is
assembled by five parts: MS-SL, aaIRES (anti-anti-IRES), aptamer, aIRES
(anti-IRES), IRES.
The IRES, aIRES,
aaIRES parts are settled, we get aptamer sequence according to
customer’s quests from aptamer database and the MS-SL is paired to the
combination part of aaIRES and aptamer. Then adjust the MS-SL part’s
length to fit it’s free energy to -11.7 kcal/mol.
Down regulated:
The differences
from down regulated to up regulated riboswitch are the order between
aptamer and aaIRES, the sequence of MS part. The new structure is showed
below:
We set MS to
“CCUCU” under experimental data and the aptamer still comes from aptamer
database.
Algorithm about free energy calculation comes
from Turner’s team:
Hairpin loops:
In this equation, n
(5) is the number of nucleotides in loop, the terminal mismatch
parameter is the sequence-dependent term for the first mismatch stacking
on the terminal base pair.
Watson-Crick
Helices:
Specific data can
be found on web site:
http://rna.urmc.rochester.edu/NNDB/turner04/index.html
References:
1.Elbashir SM et
al. (2001) Duplexes of 21-nucleotide RNAs mediate RNA interference in
cultured mammalian cells. Nature. 411:494-498.
2.Elbahir SM et al.
(2001). Functional anatomy of siRNAs for mediating efficient RNAi in
Drosophila melanogaster embryo lysate. EMBO J. 20:6877-6888.
3.Elbashir SM et
al. (2002). Analysis of gene function in somatic mammalian cells using
small interfering RNAs. Methods. 26:199-213.
4.Reynolds A, Leake
D, Boese Q, Scaringe S, Marshall WS, Khvorova A. Rational siRNA design
for RNA interference. Nat Biotechnol. 2004 Mar;22(3):326-30.
5.Ogawa, A. (2011).
Rational design of artificial riboswitches based on ligand-dependent
modulation of internal ribosome entry in wheat germ extract and their
applications as label-free biosensors. RNA (New York, N.Y.), 17(3),
478-88. doi:10.1261/rna.2433111
6.Ogawa, A. (2012).
Rational construction of eukaryotic OFF-riboswitches that downregulate
internal ribosome entry site-mediated translation in response to their
ligands. Bioorganic & medicinal chemistry letters, 22(4), 1639-42.
Elsevier Ltd. doi:10.1016/j.bmcl.2011.12.118
7.Turner, D. H. &
Mathews, D. H. (2009).
NNDB: The nearest neighbor parameter database for predicting
stability of nucleic acid secondary structure.
Nucleic Acids Research.
38, D280-D282.