NAGY, B., Martin POLÁK, O. OZOHANICS, Z. ZAMBO, E. SZABO, A. HUBERT, F. JORDAN, Jiří NOVÁČEK, V. ADAM-VIZI and A. AMBRUS. Structure of the dihydrolipoamide succinyltransferase (E2) component of the human alpha-ketoglutarate dehydrogenase complex (hKGDHc) revealed by cryo-EM and cross-linking mass spectrometry: Implications for the overall hKGDHc structure. Biochimica et Biophysica Acta - General Subjects. Amsterdam: Elsevier B.V., 2021, vol. 1865, No 6, p. 129889-129903. ISSN 0304-4165. Available from: https://dx.doi.org/10.1016/j.bbagen.2021.129889.
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Basic information
Original name Structure of the dihydrolipoamide succinyltransferase (E2) component of the human alpha-ketoglutarate dehydrogenase complex (hKGDHc) revealed by cryo-EM and cross-linking mass spectrometry: Implications for the overall hKGDHc structure
Authors NAGY, B., Martin POLÁK (203 Czech Republic, belonging to the institution), O. OZOHANICS, Z. ZAMBO, E. SZABO, A. HUBERT, F. JORDAN, Jiří NOVÁČEK (203 Czech Republic, guarantor, belonging to the institution), V. ADAM-VIZI and A. AMBRUS.
Edition Biochimica et Biophysica Acta - General Subjects, Amsterdam, Elsevier B.V. 2021, 0304-4165.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10608 Biochemistry and molecular biology
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.117
RIV identification code RIV/00216224:14740/21:00124433
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1016/j.bbagen.2021.129889
UT WoS 000640021000013
Keywords in English alpha-Ketoglutarate dehydrogenase complex; 2-Oxoglutarate dehydrogenase complex; Dihydrolipoamide succinyltransferase; Cryo-electron microscopy; Cross-linking mass spectrometry
Tags CF CRYO, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 23/3/2022 09:49.
Abstract
Background: The human mitochondrial alpha-ketoglutarate dehydrogenase complex (hKGDHc) converts KG to succinyl-CoA and NADH. Malfunction of and reactive oxygen species generation by the hKGDHc as well as its E1-E2 subcomplex are implicated in neurodegenerative disorders, ischemia-reperfusion injury, E3-deficiency and cancers. Methods: We performed cryo-EM, cross-linking mass spectrometry (CL-MS) and molecular modeling analyses to determine the structure of the E2 component of the hKGDHc (hE2k); hE2k transfers a succinyl group to CoA and forms the structural core of hKGDHc. We also assessed the overall structure of the hKGDHc by negative-stain EM and modeling. Results: We report the 2.9 angstrom resolution cryo-EM structure of the hE2k component. The cryo-EM map comprises density for hE2k residues 151-386 - the entire (inner) core catalytic domain plus a few additional residues -, while residues 1-150 are not observed due to the inherent flexibility of the N-terminal region. The structure of the latter segment was also determined by CL-MS and homology modeling. Negative-stain EM on in vitro assembled hKGDHc and previous data were used to build a putative overall structural model of the hKGDHc. Conclusions: The E2 core of the hKGDHc is composed of 24 hE2k chains organized in octahedral (8 x 3 type) assembly. Each lipoyl domain is oriented towards the core domain of an adjacent chain in the hE2k homotrimer. hE1k and hE3 are most likely tethered at the edges and faces, respectively, of the cubic hE2k assembly. General significance: The revealed structural information will support the future pharmacologically targeting of the hKGDHc.
Links
LM2018127, research and development projectName: Česká infrastruktura pro integrativní strukturní biologii (Acronym: CIISB)
Investor: Ministry of Education, Youth and Sports of the CR
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