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Multiplex glycan bead array for high throughput and high content analyses of glycan binding proteins

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Glycan-binding proteins (GBPs) play critical roles in diverse cellular functions such as cell adhesion, signal transduction and immune response. Studies of the interaction between GBPs and glycans have been hampered by the availability of high throughput and high-content technologies. Here we report multiplex glycan bead array (MGBA) that allows simultaneous analyses of 384 samples and up to 500 glycans in a single assay. The specificity, sensitivity and reproducibility of MGBA are evaluated using 39 plant lectins, 13 recombinant anti-glycan antibodies, and mammalian GBPs. We demonstrate the utility of this platform by the analyses of natural anti-glycan IgM and IgG antibodies in 961 human serum samples and the discovery of anti-glycan antibody biomarkers for ovarian cancer. Our data indicate that the MGBA platform is particularly suited for large population-based studies that require the analyses of large numbers of samples and glycans.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

258

Journal (Volume, Issue Number)

Nature communications (Volume 9, Issue 1)

Publication milestones

  • Published - 12/01/2018

Publication status

Published - 12/01/2018

ISSN

2041-1723

Publication IDs

  • Scopus: 85041391574
  • PubMed: 29343722
  • ORCID: /0000-0001-9597-4374/work/54990715
  • ORCID: /0000-0003-0385-3829/work/121881150

Publication metrics

Metrics

SciVal
FWCI
2.40
SciVal
Author count
15
SciVal
citations
30
SciVal
Paper percentile
95
SciVal
Top percentile
5
Scopus
citations
Fractional count
5
Fractional count
0.33
Fractional count
10
Fractional count
0.67
Fractional count
5
Fractional count
1

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Captures
140
Mentions
3
Citation count
82

Funding Details

This work was supported by National Institute of Health (NIH)/ National Cancer Institute (NCI) grant 1 R21 CA199868 and U01CA221242 to JXS, PGW, RDC and SP, as well as the P41GM103694 to RDC.
FundersFunding numbers
FNIH
-
NCI
1 R21 CA199868, U01CA221242
RDC
P41GM103694