Evidence map›Paper›PMID 32727845›Full record

ArticleThe Journal of biological chemistry2020

Identification of an anti-SARS-CoV-2 receptor-binding domain-directed human monoclonal antibody from a naïve semisynthetic library.

Hilal Ahmad Parray, Adarsh Kumar Chiranjivi, Shailendra Asthana, Naveen Yadav, Tripti Shrivastava, Shailendra Mani, Chandresh Sharma, Preeti Vishwakarma, Supratik Das, Kamal Pindari and 4 more

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

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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

14 authors.

Hilal Ahmad ParrayTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.
Adarsh Kumar ChiranjiviTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.
Shailendra AsthanaTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.
Naveen YadavTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.
Tripti ShrivastavaTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.
Shailendra ManiTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.
Chandresh SharmaTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.
Preeti VishwakarmaTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.ORCID 0000-0001-8530-4860
Supratik DasTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.ORCID 0000-0002-7279-938X
Kamal PindariTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.
Subrata SinhaDepartment of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.
Sweety SamalTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India.
Shubbir AhmedTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India rajesh@thsti.res.in sahmed@thsti.res.in.
Rajesh KumarTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, Haryana, India rajesh@thsti.res.in sahmed@thsti.res.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a desperate need for safe and effective vaccines, therapies, and diagnostics for SARS- coronavirus 2 (CoV-2), the development of which will be aided by the discovery of potent and selective antibodies against relevant viral epitopes. Human phage display technology has revolutionized the process of identifying and optimizing antibodies, providing facile entry points for further applications. Herein, we use this technology to search for antibodies targeting the receptor-binding domain (RBD) of CoV-2. Specifically, we screened a naïve human semisynthetic phage library against RBD, leading to the identification of a high-affinity single-chain fragment variable region (scFv). The scFv was further engineered into two other antibody formats (scFv-Fc and IgG1). All three antibody formats showed high binding specificity to CoV-2 RBD and the spike antigens in different assay systems. Flow cytometry analysis demonstrated specific binding of the IgG1 format to cells expressing membrane-bound CoV-2 spike protein. Docking studies revealed that the scFv recognizes an epitope that partially overlaps with angiotensin-converting enzyme 2 (ACE2)-interacting sites on the CoV-2 RBD. Given its high specificity and affinity, we anticipate that these anti-CoV-2 antibodies will be useful as valuable reagents for accessing the antigenicity of vaccine candidates, as well as developing antibody-based therapeutics and diagnostics for CoV-2.

Indexed as

Antibody AffinityAngiotensin-Converting Enzyme 2Binding SitesEpitopesHEK293 CellsHumansImmunoglobulin GMolecular Docking SimulationPeptidyl-Dipeptidase AProtein BindingSingle-Chain AntibodiesSpike Glycoprotein, CoronavirusACE2 protein, humanAngiotensin-Converting Enzyme 2EpitopesImmunoglobulin GPeptidyl-Dipeptidase ASingle-Chain AntibodiesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2ACE2antigenIgG1infectious diseasemAbmonoclonal antibodyphage displayRBDscFvvirus

Identifiers

PMID32727845
PMCPMC7476711

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.