Kametani Fuyuki, Tahira Marina, Takao Masaki, Matsubara Tomoyasu, Hasegawa Kazuko, Yoshida Mari, Saito Yuko, Murayama Shigeo, Hasegawa Masato
Department of Brain and Neurosciences, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo, 156-8506, Japan.
Department of Clinical Laboratory and Internal Medicine, National Center of Neurology and Psychiatry, Tokyo, Japan.
Sci Rep. 2024 Oct 2;14(1):22892. doi: 10.1038/s41598-024-74130-z.
Our previous cryogenic electron microscopy (cryoEM) analysis showed that the core structures of α-synuclein filaments accumulated in brains of patients diagnosed with dementia with Lewy bodies (DLB) and multiple system atrophy (MSA) patients are different. We analyzed the post-translational modifications (PTMs) in these filaments , and examined their relationship with the core filament structures and pathological features. Besides the common PTMs in MSA and DLB filaments, acetylation, methylation, oxidation and phosphorylation were frequently detected in MSA filaments, but not in DLB filaments. Furthermore, in DLB filament cases, the processing occurred at the C-terminal side of Asp at 119 residue and Asn at 122 residue, while in MSA cases, the processing occurred at multiple sites between residues 109-123. We have previously reported that PTMs in tau filaments depend on the filament core structure. This was considered to apply to α-synuclein filaments as well. As an example, PTMs including processing sites detected in α-synuclein filaments in early-onset DLB (an atypical form, now named juvenile-onset α-synucleinopathy) brain also supported this idea. These suggests that PTMs appeared to be closely related to the specific filament core structures.
我们之前的低温电子显微镜(cryoEM)分析表明,在被诊断为路易体痴呆(DLB)的患者和多系统萎缩(MSA)患者大脑中积累的α-突触核蛋白细丝的核心结构是不同的。我们分析了这些细丝中的翻译后修饰(PTM),并研究了它们与细丝核心结构和病理特征的关系。除了MSA和DLB细丝中常见的PTM外,乙酰化、甲基化、氧化和磷酸化在MSA细丝中经常被检测到,但在DLB细丝中未被检测到。此外,在DLB细丝病例中,加工发生在119位天冬氨酸(Asp)和122位天冬酰胺(Asn)的C末端侧,而在MSA病例中,加工发生在109-123位残基之间的多个位点。我们之前曾报道,tau细丝中的PTM取决于细丝核心结构。这被认为也适用于α-突触核蛋白细丝。例如,在早发性DLB(一种非典型形式,现称为青少年型α-突触核蛋白病)大脑中α-突触核蛋白细丝中检测到的包括加工位点在内的PTM也支持了这一观点。这些表明PTM似乎与特定的细丝核心结构密切相关。