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小分子诱导的α-突触核蛋白可溶性寡聚物具有螺旋结构。

Small-Molecule-Induced Soluble Oligomers of α-Synuclein with Helical Structure.

机构信息

Department for NMR-based Structural Biology, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077, Göttingen, Germany.

Interdisciplinary Research Center HALOmem, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Str. 3, 06120, Halle/ Saale, Germany.

出版信息

Chemistry. 2017 Sep 21;23(53):13010-13014. doi: 10.1002/chem.201703001. Epub 2017 Aug 23.

Abstract

Accumulation of α-synuclein (αSyn) aggregates constitutes the hallmark of synucleinopathies including Parkinson's disease. However, many steps from the innocuous, monomeric αSyn toward misfolded oligomers and fibrillar species remain unclear. Here, we show that αSyn can form in solution α-helical oligomers, which are off-pathway to fibrillization, through interaction with the tetrapyrrole phthalocyanine tetrasulfonate. Chemical cross-linking combined with mass spectrometry reveals a large number of intermolecular cross-links along the entire αSyn sequence in the phthalocyanine tetrasulfonate-stabilized αSyn oligomers. Our study suggests that stabilization of structured oligomers by small molecules provides a viable strategy to interfere with αSyn fibrillization.

摘要

α-突触核蛋白(αSyn)聚集体的积累构成了包括帕金森病在内的突触核蛋白病的标志。然而,从无害的单体αSyn 到错误折叠的寡聚体和纤维状物种的许多步骤仍然不清楚。在这里,我们表明 αSyn 可以通过与四吡咯酞菁四磺酸盐相互作用在溶液中形成 α-螺旋寡聚体,这是偏离纤维形成的途径。化学交联结合质谱揭示了在酞菁四磺酸盐稳定的αSyn 寡聚体中沿整个αSyn 序列存在大量的分子间交联。我们的研究表明,小分子稳定的结构寡聚体为干扰αSyn 纤维形成提供了一种可行的策略。

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