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人类脑脊液蛋白质组学——优劣参半。

Proteomics of human cerebrospinal fluid - the good, the bad, and the ugly.

机构信息

Division of Neuropathology, Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA.

出版信息

Proteomics Clin Appl. 2007 Aug;1(8):805-19. doi: 10.1002/prca.200700081. Epub 2007 Jul 13.

Abstract

The development of MALDI ESI in the late 1980s has revolutionized the biological sciences and facilitated the emergence of a new discipline called proteomics. Application of proteomics to human cerebrospinal fluid (CSF) has greatly hastened the advancement of characterizing the CSF proteome as well as revealing novel protein biomarkers that are diagnostic of various neurological diseases. While impressive progressions have been made in this field, it has become increasingly clear that proteomics results generated by various laboratories are highly variable. The underlying issues are vast, including limitations and complications with heterogeneity of patients/testing subjects, experimental design, sample processing, as well as current proteomics technology. Accordingly, this review not only summarizes the current status of characterization of the human CSF proteome and biomarker discovery for major neurodegenerative disorders, i.e., Alzheimer's disease and Parkinson's disease, but also addresses a few essential caveats involved in several steps of CSF proteomics that may contribute to the variable/contradicting results reported by different laboratories. The potential future directions of CSF proteomics are also discussed with this analysis.

摘要

基质辅助激光解吸电离飞行时间质谱(MALDI-TOF)技术在 20 世纪 80 年代末的发展彻底改变了生物科学,并促成了一个名为蛋白质组学的新学科的出现。蛋白质组学在人类脑脊液(CSF)中的应用极大地加速了 CSF 蛋白质组的特征描述以及揭示各种神经疾病的新型蛋白质生物标志物的进程。尽管在这一领域取得了令人瞩目的进展,但越来越明显的是,不同实验室产生的蛋白质组学结果高度可变。潜在的问题很多,包括患者/测试对象异质性、实验设计、样本处理以及当前蛋白质组学技术的局限性和复杂性。因此,本综述不仅总结了人类 CSF 蛋白质组的特征描述以及阿尔茨海默病和帕金森病等主要神经退行性疾病的生物标志物发现的现状,还讨论了 CSF 蛋白质组学几个步骤中涉及的一些重要注意事项,这些问题可能导致不同实验室报告的结果存在差异/矛盾。通过分析还讨论了 CSF 蛋白质组学的潜在未来方向。

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