内质网
黑素体
生物发生
细胞生物学
细胞器
亚细胞定位
生物
蛋白质稳态
内体
细胞内
化学
生物化学
黑色素
细胞质
基因
作者
Ralf M. Leonhardt,Nathalie Vigneron,Christoph Rahner,Benoı̂t J. Van den Eynde,Peter Cresswell
标识
DOI:10.1074/jbc.m109.097725
摘要
Pmel17 is a melanocyte/melanoma-specific protein that subcellularly localizes to melanosomes, where it forms a fibrillar matrix that serves for the sequestration of potentially toxic reaction intermediates of melanin synthesis and deposition of the pigment. As a key factor in melanosomal biogenesis, understanding intracellular trafficking and processing of Pmel17 is of central importance to comprehend how these organelles are formed, how they mature, and how they function in the cell. Using a series of deletion and missense mutants of Pmel17, we are able to show that the integrity of the junction between the N-terminal region and the polycystic kidney disease-like domain is highly crucial for endoplasmic reticulum export, subcellular targeting, and fibril formation by Pmel17 and thus for establishing functional melanosomes.
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