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溶剂暴露的超氧化物歧化酶 1 赖氨酸残基的电荷缺失突变不会诱导培养细胞模型中的包涵体形成。

Loss of charge mutations in solvent exposed Lys residues of superoxide dismutase 1 do not induce inclusion formation in cultured cell models.

机构信息

Department of Neuroscience, Center for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, Florida, United States of America.

College of Arts and Sciences, University of Florida, Gainesville, Florida, United States of America.

出版信息

PLoS One. 2018 Nov 6;13(11):e0206751. doi: 10.1371/journal.pone.0206751. eCollection 2018.

Abstract

Mutations in superoxide dismutase 1 (SOD1) associated with familial amyotrophic lateral sclerosis (fALS) induce the protein to misfold and aggregate. Missense mutations at more than 80 different amino acid positions have been associated with disease. How these mutations heighten the propensity of SOD1 to misfold and aggregate is unclear. With so many mutations, it is possible that more than one mechanism of aggregation may be involved. Of many possible mechanisms to explain heightened aggregation, one that has been suggested is that mutations that eliminate charged amino acids could diminish repulsive forces that would inhibit aberrant protein:protein interactions. Mutations at twenty-one charged residues in SOD1 have been associated with fALS, but of the 11 Lys residues in the protein, only 1 has been identified as mutated in ALS patients. Here, we examined whether loss of positively charged surface Lys residues in SOD1 would induce misfolding and formation of intracellular inclusions. We mutated four different Lys residues (K30, K36, K75, K91) in SOD1 that are not particularly well conserved, and expressed these variants as fusion proteins with yellow fluorescent protein (YFP) to assess inclusion formation. We also assessed whether these mutations induced binding to a conformation-restricted SOD1 antibody, designated C4F6, which recognizes non-natively folded protein. Although we observed some mutations to cause enhanced C4F6 binding, we did not observe that mutations that reduce charge at these positions caused the protein to form intracellular inclusions. Our findings may have implications for the low frequency of mutations at Lys residues SOD1 in ALS patients.

摘要

超氧化物歧化酶 1(SOD1)中的突变与家族性肌萎缩侧索硬化症(fALS)有关,导致蛋白质错误折叠和聚集。在 80 多个不同的氨基酸位置发生的错义突变与疾病有关。这些突变如何增加 SOD1 错误折叠和聚集的倾向尚不清楚。由于有如此多的突变,可能涉及不止一种聚集机制。在许多可能的解释高度聚集的机制中,有人提出的一种机制是,消除带电荷氨基酸的突变可能会减少排斥力,从而抑制异常的蛋白质-蛋白质相互作用。SOD1 中的 21 个带电残基的突变与 fALS 有关,但在该蛋白的 11 个赖氨酸残基中,只有 1 个在 ALS 患者中被鉴定为突变。在这里,我们研究了 SOD1 中失去带正电荷的表面赖氨酸残基是否会诱导错误折叠和形成细胞内包涵体。我们突变了 SOD1 中四个不同的赖氨酸残基(K30、K36、K75、K91),这些残基不是特别保守,并用黄色荧光蛋白(YFP)表达这些变体,以评估包涵体的形成。我们还评估了这些突变是否诱导与构象受限的 SOD1 抗体(称为 C4F6)结合,该抗体识别非天然折叠的蛋白质。尽管我们观察到一些突变导致 C4F6 结合增强,但我们没有观察到这些突变降低这些位置的电荷会导致蛋白质形成细胞内包涵体。我们的研究结果可能对 ALS 患者 SOD1 中赖氨酸残基突变的低频率有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0baa/6219784/fbb000075b42/pone.0206751.g001.jpg

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