Mass spectrometry-intensive top-down proteomics: an update on technology advancements and biomedical applications

被引:4
作者
Xu, Tian [1 ]
Wang, Qianjie [1 ]
Wang, Qianyi [1 ]
Sun, Liangliang [1 ]
机构
[1] Michigan State Univ, Dept Chem, 578 S Shaw Lane, E Lansing, MI 48824 USA
基金
美国国家科学基金会;
关键词
CAPILLARY-ELECTROPHORESIS; ULTRAVIOLET PHOTODISSOCIATION; INTERNAL FRAGMENTS; MEMBRANE-PROTEINS; SOFTWARE TOOL; BOTTOM-UP; PROTEOFORM; HISTONE; IDENTIFICATION; SEPARATION;
D O I
10.1039/d4ay00651h
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Proteoforms are all forms of protein molecules from the same gene because of variations at the DNA, RNA, and protein levels, e.g., alternative splicing and post-translational modifications (PTMs). Delineation of proteins in a proteoform-specific manner is crucial for understanding their biological functions. Mass spectrometry (MS)-intensive top-down proteomics (TDP) is promising for comprehensively characterizing intact proteoforms in complex biological systems. It has achieved substantial progress in technological development, including sample preparation, proteoform separations, MS instrumentation, and bioinformatics tools. In a single TDP study, thousands of proteoforms can be identified and quantified from a cell lysate. It has also been applied to various biomedical research to better our understanding of protein function in regulating cellular processes and to discover novel proteoform biomarkers of diseases for early diagnosis and therapeutic development. This review covers the most recent technological development and biomedical applications of MS-intensive TDP. Substantial progress in the technological development of mass spectrometry-based top-down proteomics enabled broad biomedical applications for bettering our understanding of proteoform function in modulating diseases and development.
引用
收藏
页码:4664 / 4682
页数:19
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