4.2 Review

Top-down proteomics: challenges, innovations, and applications in basic and clinical research

期刊

EXPERT REVIEW OF PROTEOMICS
卷 17, 期 10, 页码 719-733

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/14789450.2020.1855982

关键词

Top-down Proteomics; Mass Spectrometry; Post-translational Modifications; Proteoforms; Heart Diseases

资金

  1. U.S. Foundation for the National Institutes of Health [R01 HL096971, R01 GM117058, GM125085, HL109810]
  2. Cardiovascular Research Center Training Program in Translational Cardiovascular Science [T32 HL007936-19, T32 HL007936-20]
  3. Vascular Surgery Research Training Program [T32HL110853]

向作者/读者索取更多资源

Introduction- A better understanding of the underlying molecular mechanism of diseases is critical for developing more effective diagnostic tools and therapeutics toward precision medicine. However, many challenges remain to unravel the complex nature of diseases. Areas covered- Changes in protein isoform expression and post-translation modifications (PTMs) have gained recognition for their role in underlying disease mechanisms. Top-down mass spectrometry (MS)-based proteomics is increasingly recognized as an important method for the comprehensive characterization of proteoforms that arise from alternative splicing events and/or PTMs for basic and clinical research. Here, we review the challenges, technological innovations, and recent studies that utilize top-down proteomics to elucidate changes in the proteome with an emphasis on its use to study heart diseases. Expert opinion- Proteoform-resolved information can substantially contribute to the understanding of the molecular mechanisms underlying various diseases and for the identification of novel proteoform targets for better therapeutic development . Despite the challenges of sequencing intact proteins, top-down proteomics has enabled a wealth of information regarding protein isoform switching and changes in PTMs. Continuous developments in sample preparation, intact protein separation, and instrumentation for top-down MS have broadened its capabilities to characterize proteoforms from a range of samples on an increasingly global scale.

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