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肽或异常蛋白质聚集体细胞毒性的见解:一项荟萃分析。

Insight of the cytotoxicity of the aggregates of peptides or aberrant proteins: a meta-analysis.

作者信息

Zhou Rong, Xu Bing

机构信息

Department of Chemistry, Brandeis University, Waltham, Massachusetts, United States of America.

出版信息

PLoS One. 2014 Apr 25;9(4):e95759. doi: 10.1371/journal.pone.0095759. eCollection 2014.

Abstract

Aberrant proteins or peptide aggregates form soluble oligomers or nanofibrils that can cause a wide range of amyloidosis diseases, including Alzheimer's disease (AD). The mechanisms of their cytotoxicity, however, remain controversial and poorly understood, greatly hindering the development of AD drugs. Here we report a comprehensive evaluation of the cytotoxicity of the aggregates by meta-analysis. The analysis indicates that the cytotoxicity of the aggregates converges in a narrower range in the mass concentrations than in the molar concentrations, suggesting that it is the weight of the aggregates rather than the number of the molecules that dictates the cytotoxicity. This new perspective implies that these aggregates are likely to have non-specific interactions with cells to cause cell death. The comparison of several existing theories regarding cellular volumes supports that the aggregates may result in crowding effect and increase the free energy, thus resulting in instability of the cells.

摘要

异常蛋白质或肽聚集体形成可溶性寡聚体或纳米纤维,可导致包括阿尔茨海默病(AD)在内的多种淀粉样变性疾病。然而,它们的细胞毒性机制仍存在争议且了解甚少,这极大地阻碍了AD药物的开发。在此,我们通过荟萃分析报告了对这些聚集体细胞毒性的全面评估。分析表明,聚集体的细胞毒性在质量浓度方面比在摩尔浓度方面收敛于更窄的范围,这表明决定细胞毒性的是聚集体的重量而非分子数量。这一新观点意味着这些聚集体可能与细胞发生非特异性相互作用从而导致细胞死亡。对几种现有关于细胞体积的理论的比较支持了聚集体可能导致拥挤效应并增加自由能,进而导致细胞不稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969e/4000214/72c6f1738ce8/pone.0095759.g001.jpg

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