两种错误折叠蛋白质在聚集体形成过程中的空间差异特征。

microPublication biology Pub Date : 2024-10-21 eCollection Date: 2024-01-01 DOI:10.17912/micropub.biology.001312
Jordan N Goldy, Robert T Youker
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引用次数: 0

摘要

细胞进化出了一个复杂的折叠和降解途径网络,以维持蛋白质的原生状态。如果这些途径受到破坏(如突变)或超出其能力,细胞中就会形成蛋白质聚集体。作为一种保护机制,细胞会将这些聚集的蛋白质封存到凝集素体或凝集素体样体中。在这项研究中,我们在 HEK293 细胞中共同表达了两种错误折叠的模型蛋白,并测量了蛋白酶体抑制后聚集体的形成。与在细胞中单独表达相比,我们观察到共同表达错误折叠蛋白时凝集体形成的早期时间点存在空间差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of Spatial Differences in Two Misfolded Proteins During Aggresome Formation.

Cells have evolved an elaborate network of folding and degradation pathways to maintain the native state of proteins. If these pathways are disrupted (e.g., mutation) or their capacity is exceeded then protein aggregates form in cells. Cells sequester these aggregated proteins into aggresome or aggresome-like bodies as a protective mechanism. In this study, we co-expressed two model misfolded proteins in HEK293 cells and measured aggresome formation upon proteasomal inhibition. We observed spatial differences in early time points of aggresome formation upon co-expression of the misfolded proteins compared to individual expression in cells.

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