基因亚型
生物
τ蛋白
疾病
翻译后修饰
蛋白质组学
阿尔茨海默病
计算生物学
遗传学
细胞生物学
神经科学
生物化学
酶
基因
病理
医学
作者
Hendrik Wesseling,Waltraud Mair,Mukesh Kumar,Christoph N. Schlaffner,Shaojun Tang,Pieter Beerepoot,Benoit Fatou,Amanda J. Guise,Long Cheng,Shuko Takeda,Jan Muntel,Melissa Rotunno,Simon Dujardin,Peter Davies,Kenneth S. Kosik,Bruce L. Miller,Sabina Berretta,John C. Hedreen,Lea T. Grinberg,William W. Seeley,Bradley T. Hyman,Hanno Steen,Judith A. Steen
出处
期刊:Cell
[Elsevier]
日期:2020-11-13
卷期号:183 (6): 1699-1713.e13
被引量:438
标识
DOI:10.1016/j.cell.2020.10.029
摘要
Summary
To elucidate the role of Tau isoforms and post-translational modification (PTM) stoichiometry in Alzheimer's disease (AD), we generated a high-resolution quantitative proteomics map of 95 PTMs on multiple isoforms of Tau isolated from postmortem human tissue from 49 AD and 42 control subjects. Although Tau PTM maps reveal heterogeneity across subjects, a subset of PTMs display high occupancy and frequency for AD, suggesting importance in disease. Unsupervised analyses indicate that PTMs occur in an ordered manner, leading to Tau aggregation. The processive addition and minimal set of PTMs associated with seeding activity was further defined by analysis of size-fractionated Tau. To summarize, features in the Tau protein critical for disease intervention at different stages of disease are identified, including enrichment of 0N and 4R isoforms, underrepresentation of the C terminus, an increase in negative charge in the proline-rich region (PRR), and a decrease in positive charge in the microtubule binding domain (MBD).
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