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α-突触核蛋白的淀粉样纤维催化化学反应。

Amyloid Fibers of α-Synuclein Catalyze Chemical Reactions.

机构信息

Department of Biology and Biological Engineering, Chalmers University of Technology, 412 96 Gothenburg, Sweden.

出版信息

ACS Chem Neurosci. 2023 Feb 15;14(4):603-608. doi: 10.1021/acschemneuro.2c00799. Epub 2023 Feb 6.

Abstract

Amyloid fibers of the protein α-synuclein, found in Lewy body deposits, are hallmarks of Parkinson's disease. We here show that α-synuclein amyloids catalyze biologically relevant chemical reactions in vitro. Amyloid fibers, but not monomers, of α-synuclein catalyzed hydrolysis of the model ester -nitrophenyl acetate and dephosphorylation of the model phosphoester -nitrophenyl-orthophosphate. When His50 was replaced with Ala in α-synuclein, dephosphorylation but not esterase activity of amyloids was diminished. Truncation of the protein's C-terminus had no effect on fiber catalytic efficiency. Catalytic activity of α-synuclein fibers may be a new gain-of-function that plays a role in Parkinson's disease.

摘要

在路易小体中发现的蛋白质 α-突触核蛋白的淀粉样纤维是帕金森病的标志。我们在这里表明,α-突触核蛋白淀粉样纤维在体外催化生物学相关的化学反应。α-突触核蛋白的淀粉样纤维而不是单体,催化模型酯 -硝基苯乙酸的水解和模型磷酸酯 -硝基苯-正磷酸盐的去磷酸化。当 α-突触核蛋白中的 His50 被替换为 Ala 时,淀粉样纤维的去磷酸化但不是酯酶活性降低。该蛋白 C 端的截断对纤维催化效率没有影响。α-突触核蛋白纤维的催化活性可能是一种新的功能获得,在帕金森病中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/237f/9936539/a52bc49ad046/cn2c00799_0001.jpg

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