| Literature DB >> 31794116 |
Pratyush Kumar Mishra1,2, Chang-Mo Yoo1, Eunmi Hong3, Hyun Woo Rhee1.
Abstract
Studying protein-protein interactions (PPIs) is useful for understanding cellular functions and mechanisms. Evaluating these PPIs under conditions as similar as possible to native conditions can be achieved using photo-crosslinking methods because of their on-demand ability to generate reactive species in situ by irradiation with UV light. Various fusion tag, metabolic incorporation, and amber codon suppression approaches using various crosslinkers containing aryl azide, benzophenone, and diazirines have been applied in live cells. Mass spectrometry and immunological techniques are used to identify crosslinked proteins based on their capture transient and context-dependent interactions. Herein we discuss various incorporation methods and crosslinkers that have been used for interactome mapping in live cells.Entities:
Keywords: enzymatic labeling; photo-crosslinking; protein-protein interactions; proximity labeling; unnatural amino acids
Mesh:
Substances:
Year: 2020 PMID: 31794116 DOI: 10.1002/cbic.201900600
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164