期刊
CHEMISTRY & BIOLOGY
卷 19, 期 10, 页码 1265-1277出版社
CELL PRESS
DOI: 10.1016/j.chembiol.2012.07.023
关键词
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资金
- University of Chicago
- National Science Foundation [1057092]
- Chicago Biomedical Consortium
- Searle Funds at The Chicago Community Trust
- Deutsche Forschungsgemeinschaft [FZ82, Schi 425/5-1]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1057092] Funding Source: National Science Foundation
Protein modification by ubiquitin (UB) controls diverse cellular processes. UB is conjugated to cellular proteins by sequential transfer through an E1-E2-E3 enzymatic cascade. The cross-activities of 2 E1s, 50 E2s and thousands of E3s encoded by the human genome make it difficult to identify the substrate proteins of a specific E3 enzyme in the cell. One way to solve this problem is to engineer an orthogonal UB transfer (OUT) cascade in which the engineered UB (xUB) is relayed by engineered E1, E2 and E3 enzymes (xE1, xE2, xE3) to modify the substrate proteins of a specific E3. Here, we use phage display and mutagenesis to construct xUB-xE1 and xE1-xE2 pairs that are orthogonal to the native E1 and E2 enzymes. Our work on engineering the UB transfer cascades will enable us to use OUT to map the signal transduction networks mediated by protein ubiquitination.
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