Display of the human mucinome with defined O-glycans by gene engineered cells
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Display of the human mucinome with defined O-glycans by gene engineered cells. / Nason, Rebecca; Büll, Christian; Konstantinidi, Andriana; Sun, Lingbo; Ye, Zilu; Halim, Adnan; Du, Wenjuan; Sørensen, Daniel M.; Durbesson, Fabien; Furukawa, Sanae; Mandel, Ulla; Joshi, Hiren J.; Dworkin, Leo Alexander; Hansen, Lars; David, Leonor; Iverson, Tina M.; Bensing, Barbara A.; Sullam, Paul M.; Varki, Ajit; Vries, Erik de; de Haan, Cornelis A.M.; Vincentelli, Renaud; Henrissat, Bernard; Vakhrushev, Sergey Y.; Clausen, Henrik; Narimatsu, Yoshiki.
In: Nature Communications, Vol. 12, No. 1, 4070, 2021.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Display of the human mucinome with defined O-glycans by gene engineered cells
AU - Nason, Rebecca
AU - Büll, Christian
AU - Konstantinidi, Andriana
AU - Sun, Lingbo
AU - Ye, Zilu
AU - Halim, Adnan
AU - Du, Wenjuan
AU - Sørensen, Daniel M.
AU - Durbesson, Fabien
AU - Furukawa, Sanae
AU - Mandel, Ulla
AU - Joshi, Hiren J.
AU - Dworkin, Leo Alexander
AU - Hansen, Lars
AU - David, Leonor
AU - Iverson, Tina M.
AU - Bensing, Barbara A.
AU - Sullam, Paul M.
AU - Varki, Ajit
AU - Vries, Erik de
AU - de Haan, Cornelis A.M.
AU - Vincentelli, Renaud
AU - Henrissat, Bernard
AU - Vakhrushev, Sergey Y.
AU - Clausen, Henrik
AU - Narimatsu, Yoshiki
N1 - Funding Information: This work was supported by the Lundbeck Foundation, the Novo Nordisk Foundation, the European Commission (GlycoImaging H2020-MSCA-ITN-721297, BioCapture H2020-MSCA-ITN-722171), the Danish National Research Foundation (DNRF107), the Mizutani Foundation (to Y.N.), the European Union’s Horizon 2020 Research and Innovation Program under the Marie Sklodowska-Curie grant agreement No 787684 (to C.B.), and the National Institutes of Health grant (R01GM32373 to A.V. and GM137458 to T.M.I.). Publisher Copyright: © 2021, The Author(s).
PY - 2021
Y1 - 2021
N2 - 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.
AB - 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.
U2 - 10.1038/s41467-021-24366-4
DO - 10.1038/s41467-021-24366-4
M3 - Journal article
C2 - 34210959
AN - SCOPUS:85109164107
VL - 12
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
IS - 1
M1 - 4070
ER -
ID: 274573616