Evidence map›Paper›PMID 36048314›Full record

ArticleThe protein journal2022

Biophysical and Biochemical Characterization of the Receptor Binding Domain of SARS-CoV-2 Variants.

Ritika Khatri, Hilal Ahmad Parray, Gazala Siddiqui, Adarsh Kumar Chiranjivi, Sneha Raj, Rachel Kaul, Vikas Maithil, Sweety Samal, Shubbir Ahmed

Open access · bronzeAbstract read
In one paragraph

Article in The protein journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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

9 authors at 1 institution in 1 country.

Ritika KhatriTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, Haryana, India.
Hilal Ahmad ParrayTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, Haryana, India.
Gazala SiddiquiTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, Haryana, India.
Adarsh Kumar ChiranjiviTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, Haryana, India.
Sneha RajTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, Haryana, India.
Rachel KaulTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, Haryana, India.
Vikas MaithilTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, Haryana, India.
Sweety SamalTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, Haryana, India.
Shubbir AhmedTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, Haryana, India. sahmed@thsti.res.in.ORCID 0000-0003-1655-6735
Translational Health Science and Technology Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The newly emerging SARS-CoV-2 variants are potential threat and posing new challenges for medical intervention due to high transmissibility and escaping neutralizing antibody (NAb) responses. Many of these variants have mutations in the receptor binding domain (RBD) of SARS-CoV-2 spike protein that interacts with the host cell receptor. Rapid mutation in the RBD through natural selection to improve affinity for host receptor and antibody pressure from vaccinated or infected individual will greatly impact the presently adopted strategies for developing interventions. Understanding the nature of mutations and how they impact the biophysical, biochemical and immunological properties of the RBD will help immensely to improve the intervention strategies. To understand the impact of mutation on the protease sensitivity, thermal stability, affinity for the receptor and immune response, we prepared several mutants of soluble RBD that belong to the variants of concern (VoCs) and interest (VoIs) and characterize them. Our results show that the mutations do not impact the overall structure of the RBD. However, the mutants showed increase in the thermal melting point, few mutants were more sensitive to protease degradation, most of them have enhanced affinity for ACE2 and some of them induced better immune response compared to the parental RBD.

Indexed as

COVID-19SARS-CoV-2HumansMutationPeptide HydrolasesProtein BindingSpike Glycoprotein, CoronavirusPeptide HydrolasesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2AffinityMutationsRBDReceptorSARS-CoV-2Variants

Identifiers

PMID36048314
PMCPMC9434506
OpenAlexW4294086369

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.