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Coupled Assays for Monitoring Protein Refolding in Saccharomyces cerevisiae
JoVE 杂志
生物学
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JoVE 杂志 生物学
Coupled Assays for Monitoring Protein Refolding in Saccharomyces cerevisiae
DOI:

13:52 min

July 09, 2013

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Chapters

  • 00:05Title
  • 01:46Construction of Strains Containing FFL-GFP Plasmid
  • 02:23Preparations Prior to FFL-GFP Induction and Enzymatic Recovery Assay
  • 03:48Induction of FFL-GFP
  • 06:22Enzymatic FFL-GFP Recovery Assay
  • 07:35Fluorescence Microscopy
  • 08:55Single Cell Microscopy
  • 10:47Results: Hsp104 is Required for Efficient Refolding of Heat-denatured FFL-GFP
  • 13:36Conclusion

Summary

自动翻译

This article describes the use of a firefly luciferase-GFP fusion protein to investigate in vivo protein folding in Saccharomyces cerevisiae. Using this reagent, refolding of a model heat-denatured protein can be monitored simultaneously by fluorescence microscopy and an enzymatic assay to probe the roles of proteostasis network components in protein quality control.

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