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髓鞘蛋白质组学:过去、意外和未来。

Myelin proteomics: the past, the unexpected and the future.

机构信息

Department of Pharmacy, University of Genoa, Viale Bendetto XV, 5, 16132 Genova, Italy.

出版信息

Expert Rev Proteomics. 2014 Jun;11(3):345-54. doi: 10.1586/14789450.2014.900444. Epub 2014 Apr 4.

Abstract

Myelin proteomics has been the subject of intense research over the last decade, and its profiling has achieved good results by both in-gel and mass spectrometry-based techniques. 1280 proteins have been identified, a number expected to increase. Some of the identified proteins are as yet not established as true components of myelin. There appears to be a limit in our ability to discover markers of myelin biogenesis, function and disease. Myelin can be easily isolated free of contaminants, thanks to its lipidic nature, which however necessitates pretreatment with detergents before mass spectrometry analysis. Here, the key issue of solubilization of myelin proteins for mass spectrometry measurements is addressed. An in-depth characterization of the myelin proteome would have a profound impact on our knowledge of its pathology and physiology. Future quantitative proteomic studies of the low-abundance myelin protein complement, likely representing key regulatory components, may in future provide molecular description of the dysmyelinating/demyelinating diseases.

摘要

过去十年,髓鞘蛋白质组学一直是研究的热点,基于凝胶和质谱的技术已经对其进行了很好的分析。已经鉴定出 1280 种蛋白质,预计这一数字还会增加。一些已鉴定的蛋白质目前还不能确定为髓鞘的真正组成部分。在发现髓鞘发生、功能和疾病的标志物方面,我们的能力似乎存在一定的局限性。由于髓鞘的脂质性质,很容易将其与污染物分离,但这需要在进行质谱分析之前用去污剂进行预处理。在这里,解决了用于质谱测量的髓鞘蛋白质溶解的关键问题。髓鞘蛋白质组的深入分析将对我们对其病理学和生理学的认识产生深远的影响。未来对低丰度髓鞘蛋白补体的定量蛋白质组学研究,可能代表关键的调节成分,可能为脱髓鞘/脱髓鞘疾病提供分子描述。

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