An ubiquitin-binding molecule can work as an inhibitor of ubiquitin processing enzymes and ubiquitin receptors

被引:9
|
作者
Thanh Nguyen [1 ]
Minh Ho [1 ]
Ghosh, Ambarnil [1 ]
Kim, Truc [1 ]
Yun, Sun Il [1 ]
Lee, Seung Seo [2 ]
Kim, Kyeong Kyu [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Dept Mol Cell Biol, Suwon 440746, South Korea
[2] Univ Southampton, Dept Chem, Southampton SO17 1BJ, Hants, England
基金
新加坡国家研究基金会;
关键词
Ubiquitin; Protein-protein interaction; Druggable target; Chicago sky blue 6B; Ubiquitin inhibitor; CXC4; antagonist; CELL-CYCLE CONTROL; EXTRACELLULAR UBIQUITIN; IMMUNE-SYSTEM; PROTEASOME; LIGASES; DEGRADATION; KINASES; CANCER;
D O I
10.1016/j.bbrc.2016.09.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ubiquitin pathway plays a critical role in regulating diverse biological processes, and its dysregulation is associated with various diseases. Therefore, it is important to have a tool that can control the ubiquitin pathway in order to improve understanding of this pathway and to develop therapeutics against relevant diseases. We found that Chicago Sky Blue 6B binds directly to the beta-groove, a major interacting surface of ubiquitin. Hence, it could successfully inhibit the enzymatic activity of ubiquitin processing enzymes and the binding of ubiquitin to the CXCR4, a cell surface ubiquitin receptor. Furthermore, we demonstrated that this ubiquitin binding chemical could effectively suppress the ubiquitin induced cancer cell migration by blocking ubiquitin-CXCR4 interaction. Current results suggest that ubiquitin binding molecules can be developed as inhibitors of ubiquitin-protein interactions, which will have the value not only in unveiling the biological role of ubiquitin but also in treating related diseases. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:33 / 39
页数:7
相关论文
共 50 条
  • [1] Ubiquitin-binding domains
    Hurley, James H.
    Lee, Sangho
    Prag, Gali
    BIOCHEMICAL JOURNAL, 2006, 399 : 361 - 372
  • [2] The Length of a Ubiquitin Chain: A General Factor for Selective Recognition by Ubiquitin-Binding Proteins
    Lutz, Joachim
    Hoellmueller, Eva
    Scheffner, Martin
    Marx, Andreas
    Stengel, Florian
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2020, 59 (30) : 12371 - 12375
  • [3] ATPase and ubiquitin-binding proteins of the yeast proteasome
    David M. Rubin
    Steve van Nocker
    Michael Glickman
    Olivier Coux
    Inge Wefes
    Seth Sadis
    Hongyong Fu
    Alfred Goldberg
    Richard Vierstra
    Daniel Finley*
    Molecular Biology Reports, 1997, 24 : 17 - 26
  • [4] NEMO oligomerization and its ubiquitin-binding properties
    Ivins, Frank J.
    Montgomery, Mark G.
    Smith, Susan J. M.
    Morris-Davies, Aylin C.
    Taylor, Ian A.
    Rittinger, Katrin
    BIOCHEMICAL JOURNAL, 2009, 421 : 243 - 251
  • [5] Ubiquitin-binding domains: Mechanisms of ubiquitin recognition and use as tools to investigate ubiquitin-modified proteomes
    Scott, Daniel
    Oldham, Neil J.
    Strachan, Jo
    Searle, Mark S.
    Layfield, Robert
    PROTEOMICS, 2015, 15 (5-6) : 844 - 861
  • [6] ATPase and ubiquitin-binding proteins of the yeast proteasome
    Rubin, DM
    vanNocker, S
    Glickman, M
    Coux, O
    Wefes, I
    Sadis, S
    Fu, HY
    Goldberg, A
    Vierstra, R
    Finley, D
    MOLECULAR BIOLOGY REPORTS, 1997, 24 (1-2) : 17 - 26
  • [7] Independent Interactions of Ubiquitin-Binding Domains in a Ubiquitin-Mediated Ternary Complex
    Garner, Thomas P.
    Strachan, Joanna
    Shedden, Elizabeth C.
    Long, Jed E.
    Cavey, James R.
    Shaw, Barry
    Layfield, Robert
    Searle, Mark S.
    BIOCHEMISTRY, 2011, 50 (42) : 9076 - 9087
  • [8] A context-dependent and disordered ubiquitin-binding motif
    Dreier, Jesper E.
    Prestel, Andreas
    Martins, Joao M.
    Brondum, Sebastian S.
    Nielsen, Olaf
    Garbers, Anna E.
    Suga, Hiroaki
    Boomsma, Wouter
    Rogers, Joseph M.
    Hartmann-Petersen, Rasmus
    Kragelund, Birthe B.
    CELLULAR AND MOLECULAR LIFE SCIENCES, 2022, 79 (09)
  • [9] Ubiquitin-binding autophagic receptors in yeast: Cue5 and beyond
    Mensah, Theresah Nana Ama
    Shroff, Ankit
    Nazarko, Taras Y.
    AUTOPHAGY, 2023, 19 (09) : 2590 - 2594
  • [10] MDA-9/syntenin interacts with ubiquitin via a novel ubiquitin-binding motif
    Fumihiko Okumura
    Koichi Yoshida
    Fei Liang
    Shigetsugu Hatakeyama
    Molecular and Cellular Biochemistry, 2011, 352 : 163 - 172