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Cryo-EM structures show the mechanistic basis of pan-peptidase inhibition by human α2-macroglobulin

Authors :
Daniel Luque
Theodoros Goulas
Carlos P. Mata
Soraia R. Mendes
F. Xavier Gomis-Rüth
José R. Castón
Ministerio de Ciencia, Innovación y Universidades (España)
Agencia Estatal de Investigación (España)
Comunidad de Madrid
Generalitat de Catalunya
Fundació La Marató de TV3
Ministerio de Economía y Competitividad (España)
Ministerio de Ciencia e Innovación (España)
Comunidad de Madrid (España)
Fundación La Marató TV3
Ministerio de Economía (España)
Molecular Biology Institute of Barcelona (España)
Ministerio de Ciencia e Innovación. Centro de Excelencia Severo Ochoa (España)
Ministerio de Economía, Industria y Competitividad (España)
Source :
Repisalud, Instituto de Salud Carlos III (ISCIII), Digital.CSIC. Repositorio Institucional del CSIC, instname
Publication Year :
2022
Publisher :
Proceedings of the National Academy of Sciences, 2022.

Abstract

Humanα2-macroglobulin (hα2M) is a multidomain protein with a plethoraof essential functions, including transport of signaling molecules and endopeptidaseinhibition in innate immunity. Here, we dissected the molecular mechanism of theinhibitory function of the∼720-kDa hα2M tetramer through eight cryo–electronmicroscopy (cryo-EM) structures of complexes from human plasma. In the native com-plex, the hα2M subunits are organized in twoflexible modules in expanded conforma-tion, which enclose a highly porous cavity in which the proteolytic activity ofcirculating plasma proteins is tested. Cleavage of bait regions exposed inside the cavitytriggers rearrangement to a compact conformation, which closes openings and entrapsthe prey proteinase. After the expanded-to-compact transition, which occurs indepen-dently in the four subunits, the reactive thioester bond triggers covalent linking of theproteinase, and the receptor-binding domain is exposed on the tetramer surface forreceptor-mediated clearance from circulation. These results depict the molecular mecha-nism of a unique suicidal inhibitory trap.<br />Thiswork was supported by grants from the Spanish Ministries of Economy and Com-petitivity (Grant No. BFU2017-88736-R) and of Science and Innovation (GrantNo. PID2020-113287RB-I00) and the Comunidad Aut onoma de Madrid (GrantNo. P2018/NMT-4389) to J.R.C. and by grants from Catalan and Spanish publicand private agencies (Grant Nos. BFU2019-107725-RB-I00 and 2017SGR00003;Fundaci o“La Marat odeTV3”Grant No. 201815) to F.X.G.-R. T.G. acknowledgesa Juan de la Cierva research contract (JCI-2012-13573) from the Ministry ofEconomy (MINECO) and S.R.M. a Ph.D.-fellowship (BES2016-076877) from theMinistry of Science and Innovation. The Structural Biology Unit of the MolecularBiology Institute of Barcelona (IBMB) was a Mar ıa de Maeztu Unit of Excellence(2015 to 2019) and the Centro Nacional de Biotecnolog ıa is a Severo OchoaCenter of Excellence (MINECO award SEV 2017-0712), as awarded by the Span-ish Ministry of Economy, Industry and Competitiveness.

Details

ISSN :
10916490 and 00278424
Volume :
119
Database :
OpenAIRE
Journal :
Proceedings of the National Academy of Sciences
Accession number :
edsair.doi.dedup.....8541d9ec2a54e8d191a66b846d9c6b44
Full Text :
https://doi.org/10.1073/pnas.2200102119