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特定大小的突变亨廷顿蛋白N端片段在神经元细胞中介导聚集和毒性。

Mutant huntingtin N-terminal fragments of specific size mediate aggregation and toxicity in neuronal cells.

作者信息

Ratovitski Tamara, Gucek Marjan, Jiang Haibing, Chighladze Ekaterine, Waldron Elaine, D'Ambola James, Hou Zhipeng, Liang Yideng, Poirier Michelle A, Hirschhorn Ricky R, Graham Rona, Hayden Michael R, Cole Robert N, Ross Christopher A

机构信息

Division of Neurobiology, Department of Psychiatry, Mass Spectrometry and Proteomics Facility, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA.

出版信息

J Biol Chem. 2009 Apr 17;284(16):10855-67. doi: 10.1074/jbc.M804813200. Epub 2009 Feb 9.

Abstract

Huntingtin proteolysis is implicated in Huntington disease pathogenesis, yet, the nature of huntingtin toxic fragments remains unclear. Huntingtin undergoes proteolysis by calpains and caspases within an N-terminal region between amino acids 460 and 600. We have focused on proteolytic steps producing shorter N-terminal fragments, which we term cp-1 and cp-2 (distinct from previously described cp-A/cp-B). We used HEK293 cells to express the first 511 residues of huntingtin and further define the cp-1 and cp-2 cleavage sites. Based on epitope mapping with huntingtin-specific antibodies, we found that cp-1 cleavage occurs between residues 81 and 129 of huntingtin. Affinity and size exclusion chromatography were used to further purify huntingtin cleavage products and enrich for the cp-1/cp-2 fragments. Using mass spectrometry, we found that the cp-2 fragment is generated by cleavage of huntingtin at position Arg(167). This site was confirmed by deletion analysis and specific detection with a custom-generated cp-2 site neo-epitope antibody. Furthermore, alterations of this cleavage site resulted in a decrease in toxicity and an increase in aggregation of huntingtin in neuronal cells. These data suggest that cleavage of huntingtin at residue Arg(167) may mediate mutant huntingtin toxicity in Huntington disease.

摘要

亨廷顿蛋白的蛋白水解作用与亨廷顿病的发病机制有关,然而,亨廷顿蛋白毒性片段的性质仍不清楚。亨廷顿蛋白在氨基酸460至600之间的N端区域内被钙蛋白酶和半胱天冬酶进行蛋白水解。我们专注于产生较短N端片段的蛋白水解步骤,我们将其称为cp-1和cp-2(不同于先前描述的cp-A/cp-B)。我们使用HEK293细胞来表达亨廷顿蛋白的前511个残基,并进一步确定cp-1和cp-2的切割位点。基于用亨廷顿蛋白特异性抗体进行的表位作图,我们发现cp-1切割发生在亨廷顿蛋白的第81和129位残基之间。亲和色谱和尺寸排阻色谱被用于进一步纯化亨廷顿蛋白切割产物并富集cp-1/cp-2片段。使用质谱分析,我们发现cp-2片段是由亨廷顿蛋白在精氨酸(167)位置的切割产生的。该位点通过缺失分析和用定制生成的cp-2位点新表位抗体进行特异性检测得到证实。此外,该切割位点的改变导致神经元细胞中亨廷顿蛋白的毒性降低和聚集增加。这些数据表明,亨廷顿蛋白在精氨酸(167)残基处的切割可能介导亨廷顿病中突变型亨廷顿蛋白的毒性。

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