Wang Xiaodong, Venable John, LaPointe Paul, Hutt Darren M, Koulov Atanas V, Coppinger Judith, Gurkan Cemal, Kellner Wendy, Matteson Jeanne, Plutner Helen, Riordan John R, Kelly Jeffery W, Yates John R, Balch William E
Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Cell. 2006 Nov 17;127(4):803-15. doi: 10.1016/j.cell.2006.09.043.
The pathways that distinguish transport of folded and misfolded cargo through the exocytic (secretory) pathway of eukaryotic cells remain unknown. Using proteomics to assess global cystic fibrosis (CF) transmembrane conductance regulator (CFTR) protein interactions (the CFTR interactome), we show that Hsp90 cochaperones modulate Hsp90-dependent stability of CFTR protein folding in the endoplasmic reticulum (ER). Cell-surface rescue of the most common disease variant that is restricted to the ER, DeltaF508, can be initiated by partial siRNA silencing of the Hsp90 cochaperone ATPase regulator Aha1. We propose that failure of DeltaF508 to achieve an energetically favorable fold in response to the steady-state dynamics of the chaperone folding environment (the "chaperome") is responsible for the pathophysiology of CF. The activity of cargo-associated chaperome components may be a common mechanism regulating folding for ER exit, providing a general framework for correction of misfolding disease.
真核细胞中区分折叠和错误折叠货物通过胞吐(分泌)途径运输的机制仍不清楚。我们利用蛋白质组学评估了全球囊性纤维化(CF)跨膜电导调节因子(CFTR)的蛋白质相互作用(CFTR相互作用组),结果表明Hsp90共伴侣蛋白可调节内质网(ER)中CFTR蛋白折叠的Hsp90依赖性稳定性。最常见的局限于内质网的疾病变体DeltaF508在细胞表面的挽救可通过对Hsp90共伴侣蛋白ATP酶调节因子Aha1进行部分siRNA沉默来启动。我们认为,DeltaF508未能响应伴侣蛋白折叠环境(“伴侣组”)的稳态动力学而实现能量上有利的折叠,是导致CF病理生理的原因。货物相关伴侣组成分的活性可能是调节内质网出口折叠的常见机制,为错误折叠疾病的纠正提供了一个通用框架。