The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells

Lysosomal replacement enzymes are taken up by cell surface receptors that recognize glycans, the effects of different glycan features are unknown. Here the authors present a gene engineering screen in CHO cells that allows custom N-glycan-decorated enzymes with improved circulation time and organ di...

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Main Authors: Weihua Tian, Zilu Ye, Shengjun Wang, Morten Alder Schulz, Julie Van Coillie, Lingbo Sun, Yen-Hsi Chen, Yoshiki Narimatsu, Lars Hansen, Claus Kristensen, Ulla Mandel, Eric Paul Bennett, Siamak Jabbarzadeh-Tabrizi, Raphael Schiffmann, Jin-Song Shen, Sergey Y. Vakhrushev, Henrik Clausen, Zhang Yang
Format: Article
Language:English
Published: Nature Publishing Group 2019-04-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-019-09809-3
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spelling doaj-61e178a4b78e40d9866c7f7e1c00ad4a2021-05-11T12:10:22ZengNature Publishing GroupNature Communications2041-17232019-04-0110111310.1038/s41467-019-09809-3The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cellsWeihua Tian0Zilu Ye1Shengjun Wang2Morten Alder Schulz3Julie Van Coillie4Lingbo Sun5Yen-Hsi Chen6Yoshiki Narimatsu7Lars Hansen8Claus Kristensen9Ulla Mandel10Eric Paul Bennett11Siamak Jabbarzadeh-Tabrizi12Raphael Schiffmann13Jin-Song Shen14Sergey Y. Vakhrushev15Henrik Clausen16Zhang Yang17Copenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenGlycoDisplay ApSCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenInstitute of Metabolic Disease, Baylor Scott & White Research InstituteInstitute of Metabolic Disease, Baylor Scott & White Research InstituteInstitute of Metabolic Disease, Baylor Scott & White Research InstituteCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenCopenhagen Center for Glycomics, Departments of Cellular and Molecular Medicine and Odontology, Faculty of Health Sciences, University of CopenhagenLysosomal replacement enzymes are taken up by cell surface receptors that recognize glycans, the effects of different glycan features are unknown. Here the authors present a gene engineering screen in CHO cells that allows custom N-glycan-decorated enzymes with improved circulation time and organ distribution.https://doi.org/10.1038/s41467-019-09809-3
collection DOAJ
language English
format Article
sources DOAJ
author Weihua Tian
Zilu Ye
Shengjun Wang
Morten Alder Schulz
Julie Van Coillie
Lingbo Sun
Yen-Hsi Chen
Yoshiki Narimatsu
Lars Hansen
Claus Kristensen
Ulla Mandel
Eric Paul Bennett
Siamak Jabbarzadeh-Tabrizi
Raphael Schiffmann
Jin-Song Shen
Sergey Y. Vakhrushev
Henrik Clausen
Zhang Yang
spellingShingle Weihua Tian
Zilu Ye
Shengjun Wang
Morten Alder Schulz
Julie Van Coillie
Lingbo Sun
Yen-Hsi Chen
Yoshiki Narimatsu
Lars Hansen
Claus Kristensen
Ulla Mandel
Eric Paul Bennett
Siamak Jabbarzadeh-Tabrizi
Raphael Schiffmann
Jin-Song Shen
Sergey Y. Vakhrushev
Henrik Clausen
Zhang Yang
The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells
Nature Communications
author_facet Weihua Tian
Zilu Ye
Shengjun Wang
Morten Alder Schulz
Julie Van Coillie
Lingbo Sun
Yen-Hsi Chen
Yoshiki Narimatsu
Lars Hansen
Claus Kristensen
Ulla Mandel
Eric Paul Bennett
Siamak Jabbarzadeh-Tabrizi
Raphael Schiffmann
Jin-Song Shen
Sergey Y. Vakhrushev
Henrik Clausen
Zhang Yang
author_sort Weihua Tian
title The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells
title_short The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells
title_full The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells
title_fullStr The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells
title_full_unstemmed The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells
title_sort glycosylation design space for recombinant lysosomal replacement enzymes produced in cho cells
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2019-04-01
description Lysosomal replacement enzymes are taken up by cell surface receptors that recognize glycans, the effects of different glycan features are unknown. Here the authors present a gene engineering screen in CHO cells that allows custom N-glycan-decorated enzymes with improved circulation time and organ distribution.
url https://doi.org/10.1038/s41467-019-09809-3
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