Team:LMU-Munich/Application/Protein Screening tour

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<p align="justify">[http://www.ncbi.nlm.nih.gov/pubmedterm=screening%20libraries%20to%20identify%20proteins%20with%20desired%20binding%20activities%20using%20a%20split%20gfp%20reassembeling%20assay Designer proteins], which enhance binding capacities or improve enzymatic activities, have a large potential in both research and biotechnological processes. They are usually created by constructing and screening libraries of mutated protein variants. Proteins with desired properties are selected for in functional screenings. Despite the success of the method, it is labor intensive and limited in throughput. First protein extracts need to be prepared. Second, after successful screens individual mutated proteins must be tracked back to the original strains. Our [https://2012.igem.org/Team:LMU-Munich/Spore_Coat_Proteins '''Sporo'''beads] would eliminate the need to track protein mutants, allowing researchers to screen huge quantities of mutated proteins, only identifying and sequencing these proteins after successful screening. Figures 1 and 2 offer schematics of the process of using '''Sporo'''beads for protein screening for either enzymatic or binding affinities.</p>
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<p align="justify">[http://www.ncbi.nlm.nih.gov/pubmedterm=screening%20libraries%20to%20identify%20proteins%20with%20desired%20binding%20activities%20using%20a%20split%20gfp%20reassembeling%20assay Designer proteins], which enhance binding capacities or improve enzymatic activities, have a large potential in both research and biotechnological processes. They are usually created by constructing and screening libraries of mutated protein variants. Proteins with desired properties are selected for in functional screenings. Despite the success of the method, it is labor intensive and limited in throughput. First protein extracts need to be prepared. Second, after successful screens individual mutated proteins must be tracked back to the original strains. Our '''Sporo'''beads would eliminate the need to track protein mutants, allowing researchers to screen huge quantities of mutated proteins, only identifying and sequencing these proteins after successful screening. Figures 1 and 2 offer schematics of the process of using '''Sporo'''beads for protein screening for either enzymatic or binding affinities.</p>
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Revision as of 17:06, 26 October 2012

iGEM Ludwig-Maximilians-Universität München Beadzillus

Team-LMU Photo2.jpg

The LMU-Munich team is exuberantly happy about the great success at the World Championship Jamboree in Boston. Our project Beadzillus finished 4th and won the prize for the "Best Wiki" (with Slovenia) and "Best New Application Project".

IGEM HQ LMU prize.jpg

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