| Literature DB >> 33729691 |
Chao Liu1, Ting Wu2, Xin Shu2, Shang-Tong Li3, Daniel R Wang4, Nanxi Wang4, Rong Zhou5, Hao Yang1, Hong Jiang6, Ivo A Hendriks7, Pengyun Gong1, Long Zhang2, Michael L Nielsen7, Kui Li5, Lei Wang4, Bing Yang2.
Abstract
Protein crosslinks occur endogenously such as modifications by ubiquitin-like proteins for signaling, or exogenously through genetically encoded chemical crosslinkers (GECX) for studying elusive protein-protein interactions. However, it remains challenging to identify these protein crosslinks efficiently at the proteomic scale. Herein, software OpenUaa is developed for identifying protein crosslinks generated by genetically encoded unnatural amino acids and endogenous protein conjugation. OpenUaa features inclusive and open search capability, dramatically improving identification sensitivity and coverage. Integrating GECX with OpenUaa, the direct interactome of thioredoxin is identified in Escherichia coli cells, yielding 289 crosslinked peptides and corresponding to 205 direct binding protein of thioredoxin. These identified direct binders provide evidence for thioredoxin's regulation of redox state and mitochondria energy metabolism. When identifying endogenous conjugation of small ubiquitin-like modifier (SUMO), OpenUaa also markedly improves coverage of SUMOylated peptides by ≈92%, revealing new SUMO targets. GECX-OpenUaa will enable efficient identification of direct interactomes of various proteins in live cells.Entities:
Keywords: database search engine; genetic code expansion; mass spectrometry; protein direct interactome
Year: 2021 PMID: 33729691 DOI: 10.1002/adbi.202000308
Source DB: PubMed Journal: Adv Biol (Weinh) ISSN: 2701-0198