Evidence map›Paper›PMID 24759767›Full record

ArticlemAbs

Delineating the functional map of the interaction between nimotuzumab and the epidermal growth factor receptor.

Yaima Tundidor, Claudia Patricia García-Hernández, Amaury Pupo, Yanelys Cabrera Infante, Gertrudis Rojas

Open access · goldAbstract read
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Analysis of EGFR binding hotspots for design of new EGFR inhibitory biologics.Protein science : a publication of the Protein Society · 2024
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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 1 institution in 2 countries.

Yaima TundidorSystems Biology Department; Center of Molecular Immunology; Habana, Cuba.
Claudia Patricia García-HernándezSystems Biology Department; Center of Molecular Immunology; Habana, Cuba.
Amaury PupoSystems Biology Department; Center of Molecular Immunology; Habana, Cuba.
Yanelys Cabrera InfanteSystems Biology Department; Center of Molecular Immunology; Habana, Cuba.
Gertrudis RojasSystems Biology Department; Center of Molecular Immunology; Habana, Cuba.
Center of Molecular Immunology (Cuba) · CU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular details of epidermal growth factor receptor (EGFR) targeting by nimotuzumab, a therapeutic anti-cancer antibody, have been largely unknown. The current study delineated a functional map of their interface, based on phage display and extensive mutagenesis of both the target antigen and the Fv antibody fragment. Five residues in EGFR domain III (R353, S356, F357, T358, and H359T) and the third hypervariable region of nimotuzumab heavy chain were shown to be major functional contributors to the interaction. Fine specificity differences between nimotuzumab and other anti-EGFR antibodies were revealed. Mapping information guided the generation of a plausible in silico binding model. Knowledge about the epitope/paratope interface opens new avenues for the study of tumor sensitivity/resistance to nimotuzumab and for further engineering of its binding site. The developed mapping platform, also validated with the well-known cetuximab epitope, allows a comprehensive exploration of antigenic regions and could be expanded to map other anti-EGFR antibodies.

Indexed as

Antibody SpecificityAntibodies, Monoclonal, HumanizedEpitope MappingEpitopesErbB ReceptorsHumansProtein Structure, TertiaryAntibodies, Monoclonal, HumanizedEGFR protein, humanEpitopesErbB Receptorsnimotuzumabepitope mappingmolecular modelingparatopephage displaysite-directed mutagenesis

Identifiers

PMID24759767
PMCPMC4171005
OpenAlexW2077513301

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.