Author
Listed:
- Erandi Lira-Navarrete
(BIFI, University of Zaragoza, BIFI-IQFR (CSIC) Joint Unit, Mariano Esquillor s/n)
- Matilde de las Rivas
(BIFI, University of Zaragoza, BIFI-IQFR (CSIC) Joint Unit, Mariano Esquillor s/n)
- Ismael Compañón
(Universidad de La Rioja, Centro de Investigación en Síntesis Química)
- María Carmen Pallarés
(LMA, INA, Universidad de Zaragoza)
- Yun Kong
(Copenhagen Center for Glycomics, School of Dentistry, University of Copenhagen)
- Javier Iglesias-Fernández
(Departament de Química Orgànica i IQTCUB, Universitat de Barcelona
Present address: Department of Chemistry, Britannia House, 7 Trinity Street, King's College London, London SE1 1DB, UK)
- Gonçalo J. L. Bernardes
(University of Cambridge
Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa)
- Jesús M. Peregrina
(Universidad de La Rioja, Centro de Investigación en Síntesis Química)
- Carme Rovira
(Departament de Química Orgànica i IQTCUB, Universitat de Barcelona
ICREA, Passeig Lluís Companys 23)
- Pau Bernadó
(Centre de Biochimie Structurale, INSERM U1054, CNRS UMR 5048, Université Montpellier 1 and 2)
- Pierpaolo Bruscolini
(BIFI, University of Zaragoza, BIFI-IQFR (CSIC) Joint Unit, Mariano Esquillor s/n
Universidad de Zaragoza)
- Henrik Clausen
(Copenhagen Center for Glycomics, School of Dentistry, University of Copenhagen)
- Anabel Lostao
(LMA, INA, Universidad de Zaragoza
Fundación ARAID)
- Francisco Corzana
(Universidad de La Rioja, Centro de Investigación en Síntesis Química)
- Ramon Hurtado-Guerrero
(BIFI, University of Zaragoza, BIFI-IQFR (CSIC) Joint Unit, Mariano Esquillor s/n
Fundación ARAID)
Abstract
Protein O-glycosylation is controlled by polypeptide GalNAc-transferases (GalNAc-Ts) that uniquely feature both a catalytic and lectin domain. The underlying molecular basis of how the lectin domains of GalNAc-Ts contribute to glycopeptide specificity and catalysis remains unclear. Here we present the first crystal structures of complexes of GalNAc-T2 with glycopeptides that together with enhanced sampling molecular dynamics simulations demonstrate a cooperative mechanism by which the lectin domain enables free acceptor sites binding of glycopeptides into the catalytic domain. Atomic force microscopy and small-angle X-ray scattering experiments further reveal a dynamic conformational landscape of GalNAc-T2 and a prominent role of compact structures that are both required for efficient catalysis. Our model indicates that the activity profile of GalNAc-T2 is dictated by conformational heterogeneity and relies on a flexible linker located between the catalytic and the lectin domains. Our results also shed light on how GalNAc-Ts generate dense decoration of proteins with O-glycans.
Suggested Citation
Erandi Lira-Navarrete & Matilde de las Rivas & Ismael Compañón & María Carmen Pallarés & Yun Kong & Javier Iglesias-Fernández & Gonçalo J. L. Bernardes & Jesús M. Peregrina & Carme Rovira & Pau Bernad, 2015.
"Dynamic interplay between catalytic and lectin domains of GalNAc-transferases modulates protein O-glycosylation,"
Nature Communications, Nature, vol. 6(1), pages 1-12, November.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7937
DOI: 10.1038/ncomms7937
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Citations
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Cited by:
- Pranav Kumar & Tadakimi Tomita & Thomas A. Gerken & Collin J. Ballard & Yong Sok Lee & Louis M. Weiss & Nadine L. Samara, 2024.
"A Toxoplasma gondii O-glycosyltransferase that modulates bradyzoite cyst wall rigidity is distinct from host homologues,"
Nature Communications, Nature, vol. 15(1), pages 1-14, December.
- Andrés Manuel González-Ramírez & Ana Sofia Grosso & Zhang Yang & Ismael Compañón & Helena Coelho & Yoshiki Narimatsu & Henrik Clausen & Filipa Marcelo & Francisco Corzana & Ramon Hurtado-Guerrero, 2022.
"Structural basis for the synthesis of the core 1 structure by C1GalT1,"
Nature Communications, Nature, vol. 13(1), pages 1-15, December.
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