생화학분자생물학회입니다.
Deubiquitinase Dynamics: Methodologies for Understanding Substrate Interactions
작성자
Ji Min Lee작성일자
2025-07-14조회수
1582![]() |
Name: Ji Min Lee ( jimin.lee@kaist.ac.kr ) | |
2022-present | Associate Professor, Graduate School of Medical Science & Engineering, KAIST | |
2018-2022 | Assistant Professor, Department of Molecular Biosciences, Kangwon National University | |
2016-2018 | Principal Scientist, Business Development Team, Samsung Bioepis | |
2011-2015 | Research Scientist, Therapeutic Antibody Group Samsung Advanced Institute of Technology | |
2010-2011 | Postdoctoral research fellow, Chromatin Dynamics Research Center, SNU | |
2005-2010 | Ph.D., Department of Biological Sciences, Seoul National University |
Deubiquitinase Dynamics: Methodologies for Understanding Substrate Interactions
Deubiquitinases (DUBs) are essential regulators of protein homeostasis by removing ubiquitin chains from substrate proteins, they influence cellular signaling, protein stability, and degradation. Understanding DUB-substrate interactions is critical for elucidating their functional roles and therapeutic potential. This review highlights key methodologies for investigating DUB activity and substrate interactions, including biochemical assays, fluorescence-based approaches, and in vitro deubiquitination assays. Biochemical methods, such as those measuring protein degradation rates, ubiquitination dynamics, and protein-protein interactions, provide valuable insights into DUB function and specificity. Fluorescence-based techniques, including photoconvertible reporters, fluorescent timers, and FRET, enable real-time monitoring of DUB dynamics and substrate turnover in live cells. Furthermore, in vitro deubiquitination assays provide direct mechanistic insights of DUB activity on target substrates. Despite each method provides unique insights, they also face challenges such as limited specificity or sensitivity, technical challenges, and insufficient physiological relevance. Integrating complementary approaches can enhance accuracy and provide deeper insights into DUB-substrate interactions, facilitating the development of DUB-targeted therapeutic strategies.
BMB Rep. 2025 May;58(5):191-202.
https://pubmed.ncbi.nlm.nih.gov/40058876/