Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, United States.
Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, United States; Department of Entomology, Texas A&M University, College Station, TX 77843, United States.
Biophys Chem. 2024 Mar;306:107174. doi: 10.1016/j.bpc.2024.107174. Epub 2024 Jan 7.
The progressive aggregation of misfolded proteins is the underlying molecular cause of numerous pathologies including Parkinson's disease and injection and transthyretin amyloidosis. A growing body of evidence indicates that protein deposits detected in organs and tissues of patients diagnosed with such pathologies contain fragments of lipid membranes. In vitro experiments also showed that lipid membranes could strongly change the aggregation rate of amyloidogenic proteins, as well as alter the secondary structure and toxicity of oligomers and fibrils formed in their presence. In this review, the effect of large unilamellar vesicles (LUVs) composed of zwitterionic and anionic phospholipids on the aggregation rate of insulin, lysozyme, transthyretin (TTR) and α- synuclein (α-syn) will be discussed. The manuscript will also critically review the most recent findings on the lipid-induced changes in the secondary structure of protein oligomers and fibrils, as well as reveal the extent to which lipids could alter the toxicity of protein aggregates formed in their presence.
错误折叠蛋白质的渐进聚集是包括帕金森病和转甲状腺素淀粉样变性在内的许多病理学的潜在分子原因。越来越多的证据表明,在诊断出患有此类疾病的患者的器官和组织中检测到的蛋白质沉积物含有脂质膜的片段。体外实验还表明,脂质膜可以强烈改变淀粉样蛋白的聚集率,以及改变在其存在下形成的寡聚物和原纤维的二级结构和毒性。在这篇综述中,将讨论由两性离子和阴离子磷脂组成的大单室脂质体 (LUV) 对胰岛素、溶菌酶、转甲状腺素 (TTR) 和 α-突触核蛋白 (α-syn) 聚集率的影响。本文还将批判性地回顾脂质诱导的蛋白质寡聚物和原纤维二级结构变化的最新发现,并揭示脂质在多大程度上可以改变其存在下形成的蛋白质聚集体的毒性。