Evidence map›Paper›PMID 42202234›Full record

ArticleJournal of chemical information and modeling2026

SARS-CoV-2 Spike Protein's Structural Dynamics Affect the Activity of the Bebtelovimab Antibody.

Maher Mansur, Huixiao Hong, Sachleen Singh, Zhichao Liu, Marli Azevedo, Dongying Li, Bridgett Knox, Md Rashedul Hasan, Weida Tong, Jerome Baudry and 1 more

Abstract read
In one paragraph

Article in Journal of chemical information and modeling, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Maher MansurU.S. Food and Drug Administration (FDA), National Center for Toxicological Research, 3900 NCTR Road, Jefferson, Arkansas72079, United States.
Huixiao HongU.S. Food and Drug Administration (FDA), National Center for Toxicological Research, 3900 NCTR Road, Jefferson, Arkansas72079, United States.ORCID 0000-0001-8087-3968
Sachleen SinghU.S. Food and Drug Administration (FDA), National Center for Toxicological Research, 3900 NCTR Road, Jefferson, Arkansas72079, United States.
Zhichao LiuU.S. Food and Drug Administration (FDA), National Center for Toxicological Research, 3900 NCTR Road, Jefferson, Arkansas72079, United States.
Marli AzevedoU.S. Food and Drug Administration (FDA), National Center for Toxicological Research, 3900 NCTR Road, Jefferson, Arkansas72079, United States.
Dongying LiU.S. Food and Drug Administration (FDA), National Center for Toxicological Research, 3900 NCTR Road, Jefferson, Arkansas72079, United States.ORCID 0000-0003-0721-2500
Bridgett KnoxU.S. Food and Drug Administration (FDA), National Center for Toxicological Research, 3900 NCTR Road, Jefferson, Arkansas72079, United States.
Md Rashedul HasanCenter for Drug Evaluation and Research, U.S. Food and Drug Administration, 10903 New Hampshire Avenue, Silver Spring, Maryland20993, United States.
Weida TongU.S. Food and Drug Administration (FDA), National Center for Toxicological Research, 3900 NCTR Road, Jefferson, Arkansas72079, United States.ORCID 0000-0003-3488-6148
Jerome BaudryDepartment of Biological Sciences, The University of Alabama in Huntsville, 301 Sparkman Drive, Huntsville, Alabama35899, United States.
Baitang NingU.S. Food and Drug Administration (FDA), National Center for Toxicological Research, 3900 NCTR Road, Jefferson, Arkansas72079, United States.ORCID 0000-0003-0798-0331

Funding

Intramural FDA HHS FD999999
6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) therapeutic monoclonal antibody bebtelovimab (BEB) was designed to target the spike protein of SARS-CoV-2 and block its entry into host cells via the angiotensin-converting enzyme 2 (ACE2) receptor. In this study, we used molecular modeling to predict interactions of six clinically observed viral S-protein mutants with human ACE2, as well as BEB. We found that some of these mutants could reduce the activity of BEB by changing the relative binding affinity of the viral S-protein with BEB and ACE2. This may contribute to the resistance in viral mutants to BEB. Additionally, we demonstrated that this effect is highly dependent on the dynamic behavior of the involved proteins and their structural variations. We further assessed BEB's activity against SARS-CoV-2 Omicron subvariants BQ.1 and BQ.1.1. Our study provides insights into how mutations may affect BEB's activity, offering valuable information for the development of future therapeutics against rapidly mutating pathogens.

Indexed as

Angiotensin-Converting Enzyme 2Antibodies, Monoclonal, HumanizedSpike Glycoprotein, CoronavirusHumansSARS-CoV-2ACE2 protein, humanAngiotensin-Converting Enzyme 2Antibodies, Monoclonal, HumanizedetesevimabSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID42202234
PMCPMC13242228

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.