Atomic Structure of the E2 Inner Core of Human Pyruvate Dehydrogenase Complex

Jiansen Jiang, Flavius L. Baiesc, Yasuaki Hiromasa, Xuekui Yu, Wong Hoi Hui, Xinghong Dai, Thomas E. Roche, Z. Hong Zhou

研究成果: ジャーナルへの寄稿記事

1 引用 (Scopus)

抄録

Pyruvate dehydrogenase complex (PDC) is a large multienzyme complex that catalyzes the irreversible conversion of pyruvate to acetyl-coenzyme A with reduction of NAD+. Distinctive from PDCs in lower forms of life, in mammalian PDC, dihydrolipoyl acetyltransferase (E2; E2p in PDC) and dihydrolipoamide dehydrogenase binding protein (E3BP) combine to form a complex that plays a central role in the organization, regulation, and integration of catalytic reactions of PDC. However, the atomic structure and organization of the mammalian E2p/E3BP heterocomplex are unknown. Here, we report the structure of the recombinant dodecahedral core formed by the C-terminal inner-core/catalytic (IC) domain of human E2p determined at 3.1 Å resolution by cryo electron microscopy (cryoEM). The structure of the N-terminal fragment and four other surface areas of the human E2p IC domain exhibit significant differences from those of the other E2 crystal structures, which may have implications for the integration of E3BP in mammals. This structure also allowed us to obtain a homology model for the highly homologous IC domain of E3BP. Analysis of the interactions of human E2p or E3BP with their adjacent IC domains in the dodecahedron provides new insights into the organization of the E2p/E3BP heterocomplex and suggests a potential contribution by E3BP to catalysis in mammalian PDC.

元の言語英語
ページ(範囲)2325-2334
ページ数10
ジャーナルBiochemistry
57
発行部数16
DOI
出版物ステータス出版済み - 4 24 2018

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Pyruvate Dehydrogenase Complex
Catalytic Domain
Dihydrolipoyllysine-Residue Acetyltransferase
Multienzyme Complexes
Dihydrolipoamide Dehydrogenase
Cryoelectron Microscopy
Acetyl Coenzyme A
Mammals
Catalysis
Pyruvic Acid
NAD
Electron microscopy
Carrier Proteins
Crystal structure

All Science Journal Classification (ASJC) codes

  • Biochemistry

これを引用

Jiang, J., Baiesc, F. L., Hiromasa, Y., Yu, X., Hui, W. H., Dai, X., ... Zhou, Z. H. (2018). Atomic Structure of the E2 Inner Core of Human Pyruvate Dehydrogenase Complex. Biochemistry, 57(16), 2325-2334. https://doi.org/10.1021/acs.biochem.8b00357

Atomic Structure of the E2 Inner Core of Human Pyruvate Dehydrogenase Complex. / Jiang, Jiansen; Baiesc, Flavius L.; Hiromasa, Yasuaki; Yu, Xuekui; Hui, Wong Hoi; Dai, Xinghong; Roche, Thomas E.; Zhou, Z. Hong.

:: Biochemistry, 巻 57, 番号 16, 24.04.2018, p. 2325-2334.

研究成果: ジャーナルへの寄稿記事

Jiang, J, Baiesc, FL, Hiromasa, Y, Yu, X, Hui, WH, Dai, X, Roche, TE & Zhou, ZH 2018, 'Atomic Structure of the E2 Inner Core of Human Pyruvate Dehydrogenase Complex', Biochemistry, 巻. 57, 番号 16, pp. 2325-2334. https://doi.org/10.1021/acs.biochem.8b00357
Jiang, Jiansen ; Baiesc, Flavius L. ; Hiromasa, Yasuaki ; Yu, Xuekui ; Hui, Wong Hoi ; Dai, Xinghong ; Roche, Thomas E. ; Zhou, Z. Hong. / Atomic Structure of the E2 Inner Core of Human Pyruvate Dehydrogenase Complex. :: Biochemistry. 2018 ; 巻 57, 番号 16. pp. 2325-2334.
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AB - Pyruvate dehydrogenase complex (PDC) is a large multienzyme complex that catalyzes the irreversible conversion of pyruvate to acetyl-coenzyme A with reduction of NAD+. Distinctive from PDCs in lower forms of life, in mammalian PDC, dihydrolipoyl acetyltransferase (E2; E2p in PDC) and dihydrolipoamide dehydrogenase binding protein (E3BP) combine to form a complex that plays a central role in the organization, regulation, and integration of catalytic reactions of PDC. However, the atomic structure and organization of the mammalian E2p/E3BP heterocomplex are unknown. Here, we report the structure of the recombinant dodecahedral core formed by the C-terminal inner-core/catalytic (IC) domain of human E2p determined at 3.1 Å resolution by cryo electron microscopy (cryoEM). The structure of the N-terminal fragment and four other surface areas of the human E2p IC domain exhibit significant differences from those of the other E2 crystal structures, which may have implications for the integration of E3BP in mammals. This structure also allowed us to obtain a homology model for the highly homologous IC domain of E3BP. Analysis of the interactions of human E2p or E3BP with their adjacent IC domains in the dodecahedron provides new insights into the organization of the E2p/E3BP heterocomplex and suggests a potential contribution by E3BP to catalysis in mammalian PDC.

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