Chemistry-driven translocation of glycosylated proteins in mice

Cell surface glycans form various "glycan patterns" consisting of different types of glycan molecules, thus enabling strong and selective cell-to-cell recognition. We previously conjugated different N-glycans to human serum albumin to construct glycoalbumins mimicking natural glycan patterns that could selectively recognize target cells or control excretion pathways in mice. Here, we develop an innovative glycoalbumin capable of undergoing transformation and remodeling of its glycan pattern in vivo, which induces its translocation from the initial target to a second one. Replacing α(2,3)-sialylated N-glycans on glycoalbumin with galactosylated glycans induces the translocation of the glycoalbumin from blood or tumors to the intestine in mice. Such "in vivo glycan pattern remodeling" strategy can be used as a drug delivery system to promote excretion of a drug or medical radionuclide from the tumor after treatment, thereby preventing prolonged exposure leading to adverse effects. Alternatively, this study provides a potential strategy for using a single glycoalbumin for the simultaneous treatment of multiple diseases in a patient.

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Publication Details

Journal
Nature Communications
Published
2024-10-02
DOI
https://doi.org/10.1038/s41467-024-51342-5
Citations
4
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
0.94

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article

Chemistry-driven translocation of glycosylated proteins in mice

K. Yamada, Ambara R. Pradipta, Akari Mukaimine, Akiko Nakamura et al.
4 citations
Nature Communications
Glycosylation and Glycoproteins Research
0.94
article

Chemistry-driven translocation of glycosylated proteins in mice

K. Yamada, Ambara R. Pradipta, Akari Mukaimine, Akiko Nakamura, Yuriko Kusakari, Katsunori Tanaka, Tsung‐Che Chang
article en
4 citations

Abstract

Cell surface glycans form various "glycan patterns" consisting of different types of glycan molecules, thus enabling strong and selective cell-to-cell recognition. We previously conjugated different N-glycans to human serum albumin to construct glycoalbumins mimicking natural glycan patterns that could selectively recognize target cells or control excretion pathways in mice. Here, we develop an innovative glycoalbumin capable of undergoing transformation and remodeling of its glycan pattern in vivo, which induces its translocation from the initial target to a second one. Replacing α(2,3)-sialylated N-glycans on glycoalbumin with galactosylated glycans induces the translocation of the glycoalbumin from blood or tumors to the intestine in mice. Such "in vivo glycan pattern remodeling" strategy can be used as a drug delivery system to promote excretion of a drug or medical radionuclide from the tumor after treatment, thereby preventing prolonged exposure leading to adverse effects. Alternatively, this study provides a potential strategy for using a single glycoalbumin for the simultaneous treatment of multiple diseases in a patient.

Nature CommunicationsVol. 15(1)
Tokyo Institute of Technology (JP), Pioneer (United States) (US), Pioneer (Japan) (JP), RIKEN (JP)
Mizutani Foundation for Glycoscience, Japan Agency for Medical Research and Development, Astellas Pharma, Astellas Foundation for Research on Metabolic Disorders, Japan Society for the Promotion of Science
Openalex Percentile: Top 25%
Glycosylation and Glycoproteins Research
0.94
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Chemistry-driven translocation of glycosylated proteins in mice — K. Yamada, Ambara R. Pradipta, et al. · Nature Communications (2024) | TGRS Research Map | TGRS