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Revision as of 07:46, 26 September 2012
Many applications in synthetic biology demand precise control over subcellular localization, cell morphology, motility, and other such phenotypes that are only observable via microscopy. At present, engineering these properties is challenging due in large part to the inherent throughput limitation imposed by microscopy. We have developed a strategy that enables high-throughput library screening with microscopy by coupling a unique fluorescence signature with each genotype present in a library. These MiCodes (microscopy barcodes) are generated by targeting combinations of fluorophores to several organelles within yeast, and they eliminate the need to isolate and observe clonal populations separately. MiCodes can potentially scale to library sizes of 10^6 or more, and their analysis can be largely automated using existing image processing software. As a proof of principle, we applied MiCodes to the problem of finding unique pairs of protein-protein interaction parts.
== The Micodes Library ==Intro here... link to more specifications [[Team:Berkeley/Project/Micodes | here ]]
== Application: Leucine Zippers ==Intro here... link to more specifications [[Team:Berkeley/Project/LeucineZippers | here ]]
----Thanks for reading, etc... for a summary of what we've accomplished, check out our [[Team:Berkeley/Results | results]] page.
