Department of Ophthalmology, West Virginia University, Morgantown, WV, United States.
Department of Molecular Physiology and Biophysics, The University of Iowa Carver College of Medicine, Iowa City, IA, United States.
Adv Protein Chem Struct Biol. 2019;114:85-117. doi: 10.1016/bs.apcsb.2018.09.001. Epub 2018 Nov 28.
Defects in protein folding and trafficking are a common cause of photoreceptor degeneration, causing blindness. Photoreceptor cells present an unusual challenge to the protein folding and transport machinery due to the high rate of protein synthesis, trafficking and the renewal of the outer segment, a primary cilium that has been modified into a specialized light-sensing compartment. Phototransduction components, such as rhodopsin and cGMP-phosphodiesterase, and multimeric ciliary transport complexes, such as the BBSome, are hotspots for mutations that disrupt proteostasis and lead to the death of photoreceptors. In this chapter, we review recent studies that advance our understanding of the chaperone and transport machinery of phototransduction proteins.
蛋白质折叠和运输缺陷是导致感光细胞退化和失明的常见原因。由于蛋白质合成、运输和外节更新的速度很快,感光细胞对外界蛋白质折叠和运输机制提出了一个特殊的挑战。外节是一种特化的光感受器,已经被改造成一个专门的光感受器。视紫红质和 cGMP 磷酸二酯酶等光转导成分以及 BBSome 等多聚体纤毛运输复合物是破坏蛋白质平衡并导致感光细胞死亡的突变热点。在本章中,我们回顾了最近的研究,这些研究增进了我们对光转导蛋白伴侣和运输机制的理解。