塔姆-霍斯法尔蛋白
泌尿系统
生物
细胞生物学
功能(生物学)
解剖
作者
Gregor L. Weiss,Jessica J. Stanisich,Maximilian M. Sauer,Chia‐Wei Lin,Jonathan Eras,Dawid Zyla,Johannes Trück,Olivier Devuyst,Markus Aebi,Martin Pilhofer,Rudi Glockshuber
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2020-07-02
卷期号:369 (6506): 1005-1010
被引量:120
标识
DOI:10.1126/science.aaz9866
摘要
Uromodulin is the most abundant protein in human urine, and it forms filaments that antagonize the adhesion of uropathogens; however, the filament structure and mechanism of protection remain poorly understood. We used cryo-electron tomography to show that the uromodulin filament consists of a zigzag-shaped backbone with laterally protruding arms. N-glycosylation mapping and biophysical assays revealed that uromodulin acts as a multivalent ligand for the bacterial type 1 pilus adhesin, presenting specific epitopes on the regularly spaced arms. Imaging of uromodulin-uropathogen interactions in vitro and in patient urine showed that uromodulin filaments associate with uropathogens and mediate bacterial aggregation, which likely prevents adhesion and allows clearance by micturition. These results provide a framework for understanding uromodulin in urinary tract infections and in its more enigmatic roles in physiology and disease.
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