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The ubiquitin proteoform problem
- Source :
- Curr Opin Chem Biol
- Publication Year :
- 2021
- Publisher :
- Elsevier BV, 2021.
-
Abstract
- The diversity of ubiquitin modifications is immense. A protein can be monoubiquitylated, multi-monoubiquitylated, and polyubiquitylated with chains varying in size and shape. Ubiquitin itself can be adorned with other ubiquitin-like proteins and smaller functional groups. Considering different combinations of post-translational modifications can give rise to distinct biological outcomes, characterizing ubiquitylated proteoforms of a given protein is paramount. In this Opinion, we review recent advances in detecting and quantifying various ubiquitin proteoforms using mass spectrometry.
- Subjects :
- Proteomics
0301 basic medicine
Proteome
Protein Conformation
Computational biology
010402 general chemistry
Top-down proteomics
01 natural sciences
Biochemistry
Article
Mass Spectrometry
Substrate Specificity
Analytical Chemistry
03 medical and health sciences
Ubiquitin
Humans
Binding Sites
biology
Lysine
fungi
Ubiquitination
food and beverages
A protein
0104 chemical sciences
030104 developmental biology
biology.protein
Bottom-up proteomics
Protein Processing, Post-Translational
Subjects
Details
- ISSN :
- 13675931
- Volume :
- 63
- Database :
- OpenAIRE
- Journal :
- Current Opinion in Chemical Biology
- Accession number :
- edsair.doi.dedup.....2aea6d607a478a91c6ea628e6eee45e6
- Full Text :
- https://doi.org/10.1016/j.cbpa.2021.02.015