RNA Strand Displacement In Vitro

Previously:

In 2011, Lulu Qian and Erik Winfree of Caltech, published a paper "Scaling Up Digital Circuit Computation with DNA Strand Displacement cascades." This paper demonstrated how scalable DNA strand displacement based logic circuits are capable of processing functions as difficult as square roots.

MIT iGEM 2012:

Before our team attempted to bring the mechanism of strand displacement into an in vivo context, we first decided to try assaying strand displacement in vitro using RNA. We used 2'-O-Methyl RNA strands that have never been proved before to strand displace in vitro. Before creating our own constructs, we decided to use sequences from Qian/Winfree and adapt them to RNA.

Foundational Experiment:

Figure A shows a foundational experiment with RNA strand displacement in vitro, performed on a plate reader. The negative control, in black, is a well that receives just an anneal reporter complex. This reporter has gate strand T*S6* that is tagged with a fluorophore, 3' ROX. The top strand of the complex, the output strand, S6 which is complementary to S6*, is tagged with a quencher, that absorbs fluorescence from the fluorophore. When the two strands of the reporter are annealed, no fluorescence should be observed. The positive control, in red, is the input strand, TS6, annealed to the gate strand, T*S6* tagged with ROX. This is what we would expect the product of a strand displacement reaction to behave like. We can see that in the experimental well when the input is present, it can bind to the exposed T* domain of the reporter and displace the output, S6-quencher, strand yielding a fluorescent complex and waste.
Figure A

Nucleic Acid Delivery


To be able to achieve RNA strand displacement logic cascades in vivo, first our team had to ensure that we are capable to delivering nucleic acid to Mammalian Cells. We have achieved the delivery of plasmid DNA, single stranded modified RNA and double stranded modified RNA to mammalian cells through both lipofection and nucleofection.

Delivery of Plasmid DNA to Mammalian Cells

Through the Gateway method, we have assembled many promoter-gene constructs as detailed on our Parts Page. After construction, we deliver the plasmid DNA to Mammalian Cells through the use of transient transfection, lipofection with Lipofectamine 2000 reagent. Figure A shows:

Figure A will go here.



Delivery of 2'-O-Me RNA to Mammalian Cells

Since our modified reporter constructs use 2'-O-Methyl RNA, we must be able to deliver 2'-O-Me RNA into Mammalian Cells.


15,20,25,30 pmol ratio data from FACS

Inducible Control of Protein Expression

DOX curve

Delivery of Plasmid DNA which transcribes short RNA Inputs

FF1 Knockdown Data

In Vivo RNA Strand Displacement

Strategy 1: Lipofectamine 2000 Transfection of RNA version of Reporter from Winfree/QIan 2011 Paper


Images will go here from April 24th experiment - display red fluorescence in all wells, including those that only got reporter or the wrong input - also see red vesicles indicating reporter comes apart inside the vesicles


Strategy 2: Switch Transfection reagent to RNAiMAX

RNAiMAX is supposed to be a better transfection reagent for double stranded RNA

Images will go here from experiment from June 13th onward where we do not see red vesicles, however we still see whole cell red fluorescence

Strategy 3: Tag RNA strand with an Alexa Fluorophore to act as a transfection marker

Strategy 4: Create DNA plasmids driving transcription of RNA inputs, while transfecting RNA Reporter

Strategy 4: Nucleofect RNA reporter, RNA inputs

[Strategy 5]: Redesign RNA Reporter