Evidence map›Paper›PMID 30397147›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Site-selective chemoenzymatic glycoengineering of Fab and Fc glycans of a therapeutic antibody.

John P Giddens, Joseph V Lomino, David J DiLillo, Jeffrey V Ravetch, Lai-Xi Wang

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

63 citing papers in PubMed, 1 synthesis or guideline pooled it, 96 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Selective fluorination of Fc glycans enhances antibody-mediated effector functions.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Molecular determinants of sialylated IgG anti-inflammatory activity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. A Robust α-l-Fucosidase fromACS chemical biology · 2024
    Article
  17. A metabolic inhibitor blocks cellular fucosylation and enables production of afucosylated antibodies.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  18. Review
  19. Increased expression of SSEA-4 on TKI-resistant non-small cell lung cancer with EGFR-T790M mutation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  20. Frontiers in immunology · 2024
    Article

3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

John P GiddensDepartment of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742.
Joseph V LominoInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD 21201.
David J DiLilloLaboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, NY 10065.
Jeffrey V RavetchLaboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, NY 10065 ravetch@mail.rockefeller.edu wang518@umd.edu.ORCID 0000-0003-2024-9041
Lai-Xi WangDepartment of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742; ravetch@mail.rockefeller.edu wang518@umd.edu.
University of Maryland, Baltimore · USRockefeller University · US

Funding

Molecular mechanisms of antibody-mediated immunotherapiesR35CA196620 · NCI · ROCKEFELLER UNIVERSITY · PI JEFFREY Victor RAVETCH · 2016 to 2026
$11.5M
Personalized Immunotherapy of Patients with Ovarian CancerP01CA190174 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SABBATINI, PAUL J, SPRIGGS, DAVID R · 2015 to 2019
$10.5M
Covergent Chemoenzymatic Synthesis of Glycopeptides and GlycoproteinsR01GM080374 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI WANG, LAI-XI · 2007 to 2021
$3.9M
Synthesis and Function of Antibody Fc Domain GlycoformsR01GM096973 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI WANG, LAI-XI · 2011 to 2020
$2.4M
NCI NIH HHS P01 CA190174NCI NIH HHS R35 CA196620NIGMS NIH HHS R01 GM080374NIGMS NIH HHS R01 GM096973
6 · The paper itself

Abstract

The N-glycans attached to the Fab and Fc domains play distinct roles in modulating the functions of antibodies. However, posttranslational site-selective modifications of glycans in antibodies and other multiply glycosylated proteins remain a challenging task. Here, we report a chemoenzymatic method that permits independent manipulation of the Fab and Fc N-glycans, using cetuximab as a model therapeutic monoclonal antibody. Taking advantage of the substrate specificity of three endoglycosidases (Endo-S, Endo-S2, and Endo-F3) and their glycosynthase mutants, together with an unexpected substrate site-selectivity of a bacterial α1,6-fucosidase from

Indexed as

Antibodies, MonoclonalAntibody-Dependent Cell CytotoxicityCetuximabGlycoside HydrolasesGlycosylationHumansImmunoglobulin Fab FragmentsImmunoglobulin Fc FragmentsPolysaccharidesProtein EngineeringSubstrate SpecificityAntibodies, MonoclonalCetuximabGlycoside HydrolasesImmunoglobulin Fab FragmentsImmunoglobulin Fc FragmentsPolysaccharidesantibody glycosylationantibody therapyFc receptorglycoengineeringN-glycan

Identifiers

PMID30397147
PMCPMC6255169
OpenAlexW2900029851

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.