A Method for the Acute and Rapid Degradation of Endogenous Proteins.
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Authors
Clift, Dean
McEwan, William A
Labzin, Larisa I
Konieczny, Vera
Mogessie, Binyam
James, Leo C
Schuh, Melina
Publication Date
2017-12-14Journal Title
Cell
ISSN
0092-8674
Publisher
Elsevier BV
Volume
171
Issue
7
Pages
1692-1706.e18
Language
eng
Type
Article
This Version
VoR
Physical Medium
Print-Electronic
Metadata
Show full item recordCitation
Clift, D., McEwan, W. A., Labzin, L. I., Konieczny, V., Mogessie, B., James, L. C., & Schuh, M. (2017). A Method for the Acute and Rapid Degradation of Endogenous Proteins.. Cell, 171 (7), 1692-1706.e18. https://doi.org/10.1016/j.cell.2017.10.033
Abstract
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.
Keywords
CRISPR/Cas9, RNAi, antibodies, cell division, macrophages, meiosis, oocytes, primary cells, protein degradation, protein knockdown, Animals, Antibodies, Biochemistry, Protein Transport, Proteolysis
Sponsorship
Wellcome Trust (206248/Z/17/Z)
Identifiers
External DOI: https://doi.org/10.1016/j.cell.2017.10.033
This record's URL: https://www.repository.cam.ac.uk/handle/1810/286853
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