Evidence map›Paper›PMID 36437440›Full record

ArticleMolecular biotechnology2023

Molecular Cloning, Expression, Sequence Characterization and Structural Insight of Bubalus bubalis Growth Hormone-Receptor.

Roquyya Gul, Muhammad Umair Hanif, Faiza Gul, Hafiz Muzzammel Rehman, Mahjabeen Saleem, Muhammad Sarfaraz Ahmad, Muhammad Usman Mirza

Abstract read
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Article in Molecular biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

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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

7 authors at 4 institutions in 3 countries.

Roquyya GulGulab Devi Educational Complex, Ferozepur Road Lahore, Lahore, Pakistan. roquyya@yahoo.com.ORCID http://orcid.org/0000-0002-5294-8421
Muhammad Umair HanifGulab Devi Educational Complex, Ferozepur Road Lahore, Lahore, Pakistan.
Faiza GulSchool of Biological Sciences, University of the Punjab, Lahore, Pakistan.
Hafiz Muzzammel RehmanAlnoorians Group of Institutes, 55-Elahi Bukhsh Park, Amir Road, Shad Bagh, Lahore, Pakistan.
Mahjabeen SaleemSchool of Medical Laboratory Technology, Minhaj University Lahore, Lahore, Pakistan.
Muhammad Sarfaraz AhmadDrug Design and Development Research Group (DDDRG), Department of Chemistry, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Muhammad Usman MirzaDepartment of Chemistry and Biochemistry, University of Windsor, ON, Canada.
University of the Punjab · PKMinhaj University Lahore · PKUniversity of Malaya · MYUniversity of Windsor · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current study focuses on molecular cloning, expression and structural characterization of growth hormone-receptor (GHR) and its extracellular domain as growth hormone binding protein (GHBP) from the liver of Nili-Ravi buffalo (Bubalus bubalis; Bb). RNA was isolated, genes were amplified by reverse transcriptase-polymerase chain reaction and sequence was characterized. The BbGHR sequence showed three amino acid variations in the extracellular domain when compared with Indian BbGHR. For the production of full length BbGHR and BbGHBP in Escherichia coli (E. coli) BL21 (RIPL) Codon Plus, expression plasmids were constructed under the control of T7lac promoter and isopropyl β-D thiogalactopyranoside was used as an inducer. BbGHR and BbGHBP were expressed as inclusion bodies at ~ 40% and > 30% of the total E. coli proteins, respectively. The BbGHBP was solubilized and refolded by dilution method using cysteine-cystine redox potential. The recombinant BbGHBP was purified and biological activity was checked on HeLa cell lines showing increase cell proliferation in the presence of ovine GH (oGH), hence justifying the increase in the half-life of GH in the presence of BbGHBP. For the molecular interactions of oGH-BbGHBP multiple docking programs were employed to explore the subsequent interactions which showed high binding affinity and presence of large number of hydrogen bonds. Molecular Dynamics studies performed to examine the stability of proteins and exhibited stable structures along with favorable molecular interactions. This study has described the sequence characterization of BbGHR in Nili-Ravi buffaloes and hence provided the basis for the assessment of GH-GHR binding in other Bovidae species.

Indexed as

BuffaloesReceptors, SomatotropinAnimalsCloning, MolecularEscherichia coliGrowth HormoneHeLa CellsHumansSheepGrowth HormoneReceptors, SomatotropinGHBPGHRHeLa cell linesMolecular Dynamics SimulationNili-Ravi buffalo

Identifiers

PMID36437440
OpenAlexW4310276493

What OpenQuestion holds

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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.