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Mass spectrometry-intensive top-down proteomics: an update on technology advancements and biomedical applications.
Xu, Tian; Wang, Qianjie; Wang, Qianyi; Sun, Liangliang.
Affiliation
  • Xu T; Department of Chemistry, Michigan State University, 578 S Shaw Lane, East Lansing, MI 48824, USA. lsun@chemistry.msu.edu.
  • Wang Q; Department of Chemistry, Michigan State University, 578 S Shaw Lane, East Lansing, MI 48824, USA. lsun@chemistry.msu.edu.
  • Wang Q; Department of Chemistry, Michigan State University, 578 S Shaw Lane, East Lansing, MI 48824, USA. lsun@chemistry.msu.edu.
  • Sun L; Department of Chemistry, Michigan State University, 578 S Shaw Lane, East Lansing, MI 48824, USA. lsun@chemistry.msu.edu.
Anal Methods ; 16(28): 4664-4682, 2024 Jul 18.
Article in En | MEDLINE | ID: mdl-38973469
ABSTRACT
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mass Spectrometry / Proteomics Limits: Animals / Humans Language: En Journal: Anal Methods Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mass Spectrometry / Proteomics Limits: Animals / Humans Language: En Journal: Anal Methods Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom