Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Sweet spots in functional glycomics.

James C Paulson1, Ola Blixt, Brian E Collins

  • 1Department of Molecular Biology, The Scripps Research Institute, La Jolla, California 92037, USA. jpaulson@scripps.edu

Nature Chemical Biology
|April 19, 2006
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Vaccination elicits HIV broadly neutralizing antibodies in primates.

Nature·2026
Same author

Translating Innovation to Clinic: End-to-End Bioprocess Development and cGMP Manufacturing of N332-GT5 HIV Vaccine Candidate for First-in-Human Trials HVTN144.

bioRxiv : the preprint server for biology·2026
Same author

Diverse germline-targeting HIV Env immunogens select for distinct mutations in the same knock-in mice B cell receptors.

Nature communications·2026
Same author

Chemoenzymatic Synthesis of N-Linked Glycan Receptors of H1N1 Influenza Virus on Human Airway Epithelial Cells.

Journal of the American Chemical Society·2026
Same author

Fatal human H3N8 influenza virus has a moderate pandemic risk.

PLoS pathogens·2026
Same author

Virus glycoprotein nanodisc platform for vaccine analytics.

Nature communications·2026

Glycan-binding proteins (GBPs) decode information in the mammalian glycome. New tools help identify GBP glycan ligands and understand their functions in biological processes.

Area of Science:

  • Glycobiology
  • Molecular Biology
  • Cell Biology

Background:

  • Glycan-binding proteins (GBPs) are crucial for diverse biological functions, including cell signaling and host-pathogen interactions.
  • Identifying specific glycan ligands and understanding their influence on GBP function remains a significant challenge.
  • Low-affinity protein-glycan interactions often require multivalent binding for biological activity.

Purpose of the Study:

  • To highlight recent advancements in identifying glycan ligands for GBPs.
  • To elucidate the mechanisms underlying GBP function in biological contexts.
  • To address the challenges in understanding the specificity and impact of glycan recognition.

Main Methods:

  • Development and application of advanced glycan arrays.

Related Experiment Videos

  • Synthesis of multivalent glycan ligands for studying binding affinities.
  • Bioengineering of cell-surface glycans to mimic in vivo conditions.
  • Utilizing glycomics databases for comprehensive ligand identification.
  • Main Results:

    • New tools are enabling more precise identification of GBP glycan ligands.
    • Understanding of how multivalent interactions and other factors influence functional ligand recognition is improving.
    • Mechanisms of GBP participation in cellular processes are being elucidated.

    Conclusions:

    • Recent technological advances provide powerful new approaches to study glycan-protein interactions.
    • These tools are essential for deciphering the functional roles of GBPs in health and disease.
    • Further research will deepen our understanding of the mammalian glycome and GBP-mediated signaling.