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| - | + | Microscopy is a versatile and widely used imaging technology. Microscopy allows us to observe various phenotypes that are not observable using other techniques. For example, microscopy can show us how cells move around in their environment, how they are shaped and form networks with other cells and how proteins and other metabolites can be spatially localized inside cells. Overall, microscopy can provide us much of the information we would need in order to understand how cells behave. </p> | |
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This is due to our current limitation of guessing which parameters to choose to optimize a given system. By using libraries, we can examine a large parameter space and find trends present in our system and even optimal parameters to use for our design. | This is due to our current limitation of guessing which parameters to choose to optimize a given system. By using libraries, we can examine a large parameter space and find trends present in our system and even optimal parameters to use for our design. | ||
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Revision as of 00:06, 4 October 2012
MiCodes: Enabling library screens with microscopy by connecting genotypes to observable phenotypes
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.
Microscopy is a versatile and widely used imaging technology. Microscopy allows us to observe various phenotypes that are not observable using other techniques. For example, microscopy can show us how cells move around in their environment, how they are shaped and form networks with other cells and how proteins and other metabolites can be spatially localized inside cells. Overall, microscopy can provide us much of the information we would need in order to understand how cells behave.
When we engineer systems in synthetic biology using cellular features such as motility, morphology and subcellular localization, we usually like to do so using libraries. This is due to our current limitation of guessing which parameters to choose to optimize a given system. By using libraries, we can examine a large parameter space and find trends present in our system and even optimal parameters to use for our design.
By localizing fluorescent proteins to specific organelles, each cell can be given a "microscopic barcode", or MiCode. Below you can see a single sample MiCode. Each member of a library will get a unique MiCode, distinguishing it from the rest of the library and tying the MiCode phenotype to a specific genotype.
This example MiCode has four targeted organelles: nucleus-red, vacuolar membrane-red, cellular periphery-blue, actin-green.
