| Literature DB >> 35530525 |
Hye Lin Park1, Han Yong Lee1, Gyeong Mee Yoon1.
Abstract
The precise regulation of the homeostasis of the cellular proteome is critical for the appropriate growth and development of plants. It also allows the plants to respond to various environmental stresses, by modulating their biochemical and physiological aspects in a timely manner. Ubiquitination of cellular proteins is one of the major protein degradation routes for maintaining cellular protein homeostasis, and ubiquitin E3 ligases, components of ubiquitin ligase complexes, play an important role in the selective degradation of target proteins via substrate-specific interactions. Thus, understanding the role of E3 ligases and their substrate regulation uncovers their specific cellular and physiological functions. Here, we provide protocols for auto- and substrate-ubiquitination analyses that utilize the combination of in vitro purified E3 ubiquitin ligase proteins and immunoprecipitation.Entities:
Keywords: ACC synthase; SINAT2; Self-ubiquitination; Substrate-ubiquitination; Ubiquitination
Year: 2022 PMID: 35530525 PMCID: PMC9018431 DOI: 10.21769/BioProtoc.4368
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325