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Higher-order structural characterisation of native proteins and complexes by top-down mass spectrometry.通过自上而下的质谱法对天然蛋白质和复合物进行高阶结构表征。
Chem Sci. 2020 Oct 20;11(48):12918-12936. doi: 10.1039/d0sc04392c.
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Rapid Analysis of Reduced Antibody Drug Conjugate by Online LC-MS/MS with Fourier Transform Ion Cyclotron Resonance Mass Spectrometry.在线 LC-MS/MS 联用傅里叶变换离子回旋共振质谱法快速分析抗体药物偶联物。
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Distinct hypertrophic cardiomyopathy genotypes result in convergent sarcomeric proteoform profiles revealed by top-down proteomics.不同肥厚型心肌病基因型导致的相似肌节蛋白构象表型可通过自上而下的蛋白质组学技术揭示。
Proc Natl Acad Sci U S A. 2020 Oct 6;117(40):24691-24700. doi: 10.1073/pnas.2006764117. Epub 2020 Sep 23.
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Intact Protein Mass Spectrometry for Therapeutic Protein Quantitation, Pharmacokinetics, and Biotransformation in Preclinical and Clinical Studies: An Industry Perspective.完整蛋白质质谱法在临床前和临床研究中用于治疗性蛋白质定量、药代动力学和生物转化:行业视角
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Internal Fragments Generated by Electron Ionization Dissociation Enhance Protein Top-Down Mass Spectrometry.电子电离解离产生的内部片段增强蛋白质自上而下质谱分析
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MASH Explorer: A Universal Software Environment for Top-Down Proteomics.MASH浏览器:一种用于自上而下蛋白质组学的通用软件环境。
J Proteome Res. 2020 Sep 4;19(9):3867-3876. doi: 10.1021/acs.jproteome.0c00469. Epub 2020 Aug 24.
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Nanoproteomics enables proteoform-resolved analysis of low-abundance proteins in human serum.纳米蛋白质组学能够对人血清中的低丰度蛋白质进行肽谱解析分析。
Nat Commun. 2020 Aug 6;11(1):3903. doi: 10.1038/s41467-020-17643-1.
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PEPPI-MS: Polyacrylamide-Gel-Based Prefractionation for Analysis of Intact Proteoforms and Protein Complexes by Mass Spectrometry.PEPPI-MS:基于聚丙烯酰胺凝胶的预分级用于通过质谱分析完整的蛋白形式和蛋白质复合物。
J Proteome Res. 2020 Sep 4;19(9):3779-3791. doi: 10.1021/acs.jproteome.0c00303. Epub 2020 Jul 11.
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Sensitive Top-Down Proteomics Analysis of a Low Number of Mammalian Cells Using a Nanodroplet Sample Processing Platform.利用纳升级液滴样品处理平台对少量哺乳动物细胞进行敏感的自上而下的蛋白质组学分析。
Anal Chem. 2020 May 19;92(10):7087-7095. doi: 10.1021/acs.analchem.0c00467. Epub 2020 May 6.
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Combining native and 'omics' mass spectrometry to identify endogenous ligands bound to membrane proteins.结合天然和 'omics' 质谱法鉴定与膜蛋白结合的内源性配体。
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自上而下的蛋白质组学:基础和临床研究中的挑战、创新和应用。

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

机构信息

Department of Chemistry, University of Wisconsin-Madison , Madison, Wisconsin, USA.

Department of Cell and Regenerative Biology, University of Wisconsin-Madison , Madison, Wisconsin, USA.

出版信息

Expert Rev Proteomics. 2020 Oct;17(10):719-733. doi: 10.1080/14789450.2020.1855982. Epub 2020 Dec 17.

DOI:10.1080/14789450.2020.1855982
PMID:33232185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7864889/
Abstract

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. 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. 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.

摘要

深入了解疾病的潜在分子机制对于开发更有效的诊断工具和治疗方法以实现精准医学至关重要。然而,要揭示疾病的复杂本质,仍然存在许多挑战。蛋白质异构体表达和翻译后修饰 (PTM) 的变化因其在潜在疾病机制中的作用而受到关注。基于自上而下的质谱 (MS) 的蛋白质组学越来越被认为是一种重要的方法,可用于全面表征由选择性剪接事件和/或 PTM 产生的蛋白质异构体,用于基础和临床研究。在这里,我们回顾了利用自上而下的蛋白质组学阐明蛋白质组变化的挑战、技术创新和最近的研究,重点介绍其在心脏病研究中的应用。蛋白质异构体解析信息可大大有助于理解各种疾病的分子机制,并为更好的治疗开发确定新的蛋白质异构体靶标。尽管完整蛋白质测序存在挑战,但自上而下的蛋白质组学已经提供了大量关于蛋白质异构体转换和 PTM 变化的信息。样品制备、完整蛋白质分离和自上而下 MS 仪器的不断发展,拓宽了其从各种样品中表征蛋白质异构体的能力,在全球范围内的应用范围越来越广泛。