4.8 Article

A Method for the Acute and Rapid Degradation of Endogenous Proteins

期刊

CELL
卷 171, 期 7, 页码 1692-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2017.10.033

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资金

  1. Medical Research Council [MC_U105192711, MC_U105181010]
  2. European Community's Seventh Framework Programme [241548]
  3. European Research Council (ERC) [337415]
  4. Wellcome Trust [200594/Z/16/Z]
  5. MRC [MC_U105192711, MC_U105181010] Funding Source: UKRI
  6. Medical Research Council [MC_U105181010, MC_U105192711] Funding Source: researchfish
  7. Wellcome Trust [200594/Z/16/Z] Funding Source: researchfish
  8. Wellcome Trust [200594/Z/16/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

Methods for the targeted disruption of protein function have revolutionized science and greatly expedited the systematic characterization of genes. Two main approaches are currently used to disrupt protein function: DNA knockout and RNA interference, which act at the genome and mRNA level, respectively. A method that directly alters endogenous protein levels is currently not available. Here, we present Trim-Away, a technique to degrade endogenous proteins acutely in mammalian cells without prior modification of the genome or mRNA. Trim-Away harnesses the cellular protein degradation machinery to remove unmodified native proteins within minutes of application. This rapidity minimizes the risk that phenotypes are compensated and that secondary, non-specific defects accumulate over time. Because Trim-Away utilizes antibodies, it can be applied to a wide range of target proteins using off-the-shelf reagents. Trim-Away allows the study of protein function in diverse cell types, including non-dividing primary cells where genome-and RNA-targeting methods are limited.

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