相互作用体
生物
人类蛋白质组计划
合并(版本控制)
蛋白质组
计算生物学
生物发生
蛋白质组学
线粒体膜转运蛋白
细胞生物学
线粒体
线粒体内膜
遗传学
基因
情报检索
计算机科学
作者
Metin Özdemir,Silke Oeljeklaus,Alexander Benjamin Schendzielorz,Marcel Morgenstern,Anusha Valpadashi,Roya Yousefi,Bettina Warscheid,Sven Dennerlein
摘要
The mitochondrial proteome arises from dual genetic origin. Nuclear-encoded proteins need to be transported across or inserted into two distinguished membranes, and the TOM complex represents the main translocase in the outer mitochondrial membrane. Its composition and regulations have been extensively investigated within yeast cells. However, we have little knowledge of the TOM complex composition within human cells. Here, we have defined the TOM interactome in a comprehensive manner using biochemical approaches to isolate the TOM complex in combination with quantitative mass spectrometry analyses. Within these studies, we defined the pleiotropic nature of the human TOM complex, including new interactors, such as TRABD. Our studies provide a framework to understand the various biogenesis pathways that merge at the TOM complex within human cells.
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