Display of the human mucinome with defined O-glycans by gene engineered cells

Rebecca Nason(University of Copenhagen), Christian Büll(University of Copenhagen), Andriana Konstantinidi(University of Copenhagen), Lingbo Sun(University of Copenhagen), Zilu Ye(University of Copenhagen), Adnan Halim(University of Copenhagen), Wenjuan Du(Utrecht University), Daniel Madriz Sørensen(University of Copenhagen), Fabien Durbesson(Centre National de la Recherche Scientifique), Sanae Furukawa(University of Copenhagen), Ulla Mandel(University of Copenhagen), Hiren J. Joshi(University of Copenhagen), Leo Alexander Dworkin(University of Copenhagen), Lars Hestbjerg Hansen(University of Copenhagen), Leonor David(Universidade do Porto), T.M. Iverson(Vanderbilt University), Barbara A. Bensing(San Francisco VA Medical Center), Paul M. Sullam(San Francisco VA Medical Center), Ajit Varki(University of California San Diego), Erik de Vries(Utrecht University), Cornelis A. M. de Haan(Utrecht University), Renaud Vincentelli(Centre National de la Recherche Scientifique), Bernard Henrissat(University of Copenhagen), Sergey Y. Vakhrushev(University of Copenhagen), Henrik Clausen(University of Copenhagen), Yoshiki Narimatsu(University of Copenhagen)
Nature Communications
July 1, 2021
Cited by 127Open Access
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Abstract

Mucins are a large family of heavily O-glycosylated proteins that cover all mucosal surfaces and constitute the major macromolecules in most body fluids. Mucins are primarily defined by their variable tandem repeat (TR) domains that are densely decorated with different O-glycan structures in distinct patterns, and these arguably convey much of the informational content of mucins. Here, we develop a cell-based platform for the display and production of human TR O-glycodomains (~200 amino acids) with tunable structures and patterns of O-glycans using membrane-bound and secreted reporters expressed in glycoengineered HEK293 cells. Availability of defined mucin TR O-glycodomains advances experimental studies into the versatile role of mucins at the interface with pathogenic microorganisms and the microbiome, and sparks new strategies for molecular dissection of specific roles of adhesins, glycoside hydrolases, glycopeptidases, viruses and other interactions with mucin TRs as highlighted by examples.


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