Semi-Synthetic CoA-α-Synuclein Constructs Trap N-Terminal Acetyltransferase NatB for Binding Mechanism Studies.
Journal
Journal of the American Chemical Society
ISSN: 1520-5126
Titre abrégé: J Am Chem Soc
Pays: United States
ID NLM: 7503056
Informations de publication
Date de publication:
28 06 2023
28 06 2023
Historique:
medline:
29
6
2023
pubmed:
15
6
2023
entrez:
15
6
2023
Statut:
ppublish
Résumé
N-terminal acetylation is a chemical modification carried out by N-terminal acetyltransferases. A major member of this enzyme family, NatB, acts on much of the human proteome, including α-synuclein (αS), a synaptic protein that mediates vesicle trafficking. NatB acetylation of αS modulates its lipid vesicle binding properties and amyloid fibril formation, which underlies its role in the pathogenesis of Parkinson's disease. Although the molecular details of the interaction between human NatB (hNatB) and the N-terminus of αS have been resolved, whether the remainder of the protein plays a role in interacting with the enzyme is unknown. Here, we execute the first synthesis, by native chemical ligation, of a bisubstrate inhibitor of NatB consisting of coenzyme A and full-length human αS, additionally incorporating two fluorescent probes for studies of conformational dynamics. We use cryo-electron microscopy (cryo-EM) to characterize the structural features of the hNatB/inhibitor complex and show that, beyond the first few residues, αS remains disordered when in complex with hNatB. We further probe changes in the αS conformation by single molecule Förster resonance energy transfer (smFRET) to reveal that the C-terminus expands when bound to hNatB. Computational models based on the cryo-EM and smFRET data help to explain the conformational changes as well as their implications for hNatB substrate recognition and specific inhibition of the interaction with αS. Beyond the study of αS and NatB, these experiments illustrate valuable strategies for the study of challenging structural biology targets through a combination of protein semi-synthesis, cryo-EM, smFRET, and computational modeling.
Identifiants
pubmed: 37319422
doi: 10.1021/jacs.3c03887
doi:
Substances chimiques
alpha-Synuclein
0
N-Terminal Acetyltransferases
EC 2.3.1.88
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, N.I.H., Extramural
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
14019-14030Subventions
Organisme : NINDS NIH HHS
ID : R01 NS120625
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM133398
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM118090
Pays : United States
Organisme : NINDS NIH HHS
ID : RF1 NS125770
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS103873
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM132039
Pays : United States
Organisme : NIH HHS
ID : S10 OD030460
Pays : United States
Commentaires et corrections
Type : UpdateOf