| Literature DB >> 27720676 |
Sergio Guerrero-Castillo1, Fabian Baertling2, Daniel Kownatzki3, Hans J Wessels4, Susanne Arnold3, Ulrich Brandt1, Leo Nijtmans5.
Abstract
Mitochondrial complex I is the largest integral membrane enzyme of the respiratory chain and consists of 44 different subunits encoded in the mitochondrial and nuclear genome. Its biosynthesis is a highly complicated and multifaceted process involving at least 14 additional assembly factors. How these subunits assemble into a functional complex I and where the assembly factors come into play is largely unknown. Here, we applied a dynamic complexome profiling approach to elucidate the assembly of human mitochondrial complex I and its further incorporation into respiratory chain supercomplexes. We delineate the stepwise incorporation of all but one subunit into a series of distinct assembly intermediates and their association with known and putative assembly factors, which had not been implicated in this process before. The resulting detailed and comprehensive model of complex I assembly is fully consistent with recent structural data and the remarkable modular architecture of this multiprotein complex.Entities:
Keywords: assembly; assembly factors; complex I; complexome profiling; mitochondria; oxidative phosporylation
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Year: 2016 PMID: 27720676 DOI: 10.1016/j.cmet.2016.09.002
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287