High-Resolution Structural Proteomics of Mitochondria Using the 'Build and Retrieve' Methodology.

High-Resolution Structural Proteomics of Mitochondria Using the 'Build and Retrieve' Methodology.
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DOI:
10.1016/j.mcpro.2023.100666
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发表时间:
2023-12
影响因子:
7
通讯作者:
Yu, Edward W.
Yu, Edward W.
中科院分区:
生物学1区
文献类型:
--
作者:
Zhang, Zhemin;Tringides, Marios L.;Morgan, Christopher E.;Miyagi, Masaru;Mears, Jason A.;Hoppel, Charles L.;Yu, Edward W.

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The application of integrated systems biology to the field of structural biology is a promising new direction, although it is still in the infant stages of development. Here we report the use of single particle cryo-EM to identify multiple proteins from three enriched heterogeneous fractions prepared from human liver mitochondrial lysate. We simultaneously identify and solve high-resolution structures of nine essential mitochondrial enzymes with key metabolic functions, including fatty acid catabolism, reactive oxidative species clearance, and amino acid metabolism. Our methodology also identified multiple distinct members of the acyl-CoA dehydrogenase family. This work highlights the potential of cryo-EM to explore tissue proteomics at the atomic level. Using cryo-EM to define the composition of a human mitochondrial lysate. Simultaneously identifying and solving structures of nine mitochondrial enzymes. Application of cryo-EM in studying high-resolution structural omics of human enzymes. Zhang et al use cryo-EM to simultaneously identify and solve structures of nine different enzymes from human liver mitochondrial lysate. Their work highlights the potential of this methodology in facilitating structural proteomics of a biological system at high resolution.
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