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自上而下质谱分析的未来如何?

What does the future hold for Top Down mass spectrometry?

机构信息

Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.

出版信息

J Am Soc Mass Spectrom. 2010 Feb;21(2):193-202. doi: 10.1016/j.jasms.2009.10.014. Epub 2009 Oct 29.

Abstract

Mass spectrometry (MS) research has revolutionized modern biological and biomedical fields. At the heart of the majority of mass spectrometry experiments is the use of Bottom Up mass spectrometry methods where proteins are first proteolyzed into smaller fragments before MS interrogation. The advent of electron capture dissociation and, more recently, electron-transfer dissociation, however, has allowed Top Down (analysis of intact proteins) or middle down (analysis of large polypeptides) mass spectrometry to both experience large increases in development, growth, and overall usage. Nevertheless, for high-throughput large-scale proteomic studies, Bottom Up mass spectrometry has easily dominated the field. As Top Down mass spectrometry methodology and technology continue to develop, will it genuinely be able to compete with Bottom Up mass spectrometry for whole proteome analysis? Discussed here are the current approaches, applications, issues, and future view of high-throughput Top Down mass spectrometry.

摘要

质谱(MS)研究已经彻底改变了现代生物学和生物医学领域。在大多数质谱实验的核心是使用自上而下的质谱方法,其中蛋白质首先被蛋白酶解成较小的片段,然后再进行 MS 分析。然而,电子俘获解离的出现,以及最近的电子转移解离的出现,使得自上而下(分析完整蛋白质)或中间向下(分析大多肽)的质谱技术都得到了极大的发展、增长和整体应用。尽管如此,对于高通量大规模蛋白质组学研究,自下而上的质谱技术仍然轻松占据主导地位。随着自上而下的质谱方法和技术的不断发展,它是否真的能够与自下而上的质谱技术竞争进行全蛋白质组分析?本文讨论了高通量自上而下的质谱技术的当前方法、应用、问题和未来展望。

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