Structural architecture of the acidic region of the B domain of coagulation factor V.

blood coagulation electron microscopy factor V plasma protein conformation

Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
23 Nov 2023
Historique:
received: 31 08 2023
revised: 03 11 2023
accepted: 06 11 2023
pubmed: 26 11 2023
medline: 26 11 2023
entrez: 25 11 2023
Statut: aheadofprint

Résumé

Coagulation factor (F)V features an A1-A2-B-A3-C1-C2 domain organization and functions as the inactive precursor of FVa, a component of the prothrombinase complex required for rapid thrombin generation in the penultimate step of the coagulation cascade. An intramolecular interaction within the large B domain (residues 710-1545) involves the basic region (BR, residues 963-1008) and acidic region (AR, residues 1493-1537) and locks FV in its inactive state. However, structural information on this important regulatory interaction or on the separate architecture of the AR and BR remains elusive due to conformational disorder of the B domain. To reveal the structure of the BR-AR interaction or of its separate components. The structure of FV is solved by cryogenic electron microscopy. A new 3.05 Å resolution cryogenic electron microscopy structure of FV confirms the overall organization of the A and C domains but resolves the segment 1507 to 1545 within a largely disordered B domain. The segment contains most of the AR and is organized as recently reported in FV short, a spliced variant of FV with a significantly shorter and less disordered B domain. The similar architecture of the AR in FV and FV short provides structural context for physiologically important interactions of this region with the BR in FV and with the basic C-terminal end of tissue factor pathway inhibitor α in FV short.

Sections du résumé

BACKGROUND BACKGROUND
Coagulation factor (F)V features an A1-A2-B-A3-C1-C2 domain organization and functions as the inactive precursor of FVa, a component of the prothrombinase complex required for rapid thrombin generation in the penultimate step of the coagulation cascade. An intramolecular interaction within the large B domain (residues 710-1545) involves the basic region (BR, residues 963-1008) and acidic region (AR, residues 1493-1537) and locks FV in its inactive state. However, structural information on this important regulatory interaction or on the separate architecture of the AR and BR remains elusive due to conformational disorder of the B domain.
OBJECTIVES OBJECTIVE
To reveal the structure of the BR-AR interaction or of its separate components.
METHODS METHODS
The structure of FV is solved by cryogenic electron microscopy.
RESULTS RESULTS
A new 3.05 Å resolution cryogenic electron microscopy structure of FV confirms the overall organization of the A and C domains but resolves the segment 1507 to 1545 within a largely disordered B domain. The segment contains most of the AR and is organized as recently reported in FV short, a spliced variant of FV with a significantly shorter and less disordered B domain.
CONCLUSION CONCLUSIONS
The similar architecture of the AR in FV and FV short provides structural context for physiologically important interactions of this region with the BR in FV and with the basic C-terminal end of tissue factor pathway inhibitor α in FV short.

Identifiants

pubmed: 38007061
pii: S1538-7836(23)00837-1
doi: 10.1016/j.jtha.2023.11.003
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interests There are no competing interests to disclose.

Auteurs

Bassem M Mohammed (BM)

Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, St. Louis, Missouri, USA.

Katherine Basore (K)

Washington University Center for Cellular Imaging, Washington University School of Medicine, Saint Louis, Missouri, USA.

Brock Summers (B)

Washington University Center for Cellular Imaging, Washington University School of Medicine, Saint Louis, Missouri, USA.

Leslie A Pelc (LA)

Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, St. Louis, Missouri, USA.

Enrico Di Cera (E)

Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, St. Louis, Missouri, USA. Electronic address: enrico@slu.edu.

Classifications MeSH