Design of hACE2-based small peptide inhibitors against spike protein of SARS-CoV-2: a computational approach

COVID-19 which is caused by the severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) has been declared pandemic in 2019. Though there is development of vaccines but there is an emergence requirement of drugs against SARS-CoV-2. Antiviral peptides can be rationally created and improved based...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Structural chemistry 2023-10, Vol.34 (5), p.1843-1856
Hauptverfasser: Dhingra, Naveen, Bhardwaj, Ravindra, Bhardwaj, Uma, Kapoor, Kapish
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1856
container_issue 5
container_start_page 1843
container_title Structural chemistry
container_volume 34
creator Dhingra, Naveen
Bhardwaj, Ravindra
Bhardwaj, Uma
Kapoor, Kapish
description COVID-19 which is caused by the severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) has been declared pandemic in 2019. Though there is development of vaccines but there is an emergence requirement of drugs against SARS-CoV-2. Antiviral peptides can be rationally created and improved based on the known structures of viral proteins and their biological targets. In the given study, small peptide inhibitors with three amino acids are designed and docked against SARS-CoV-2 coronavirus using molecular docking approach. All the designed peptides bind at the active site but the highest binding affinity was observed for HisGluAsp. Molecular dynamics was performed to validate the stability and interactions of compound. The molecule has followed the druglikeness properties and with highest probability of being absorbed by the gastrointestinal tract. The results of the current investigation point to the possibility that the identified small peptides may prevent SARS-CoV-2 infection, although additional wet-lab tests are still required to confirm these results.
doi_str_mv 10.1007/s11224-023-02125-z
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9875775</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A766432478</galeid><sourcerecordid>A766432478</sourcerecordid><originalsourceid>FETCH-LOGICAL-c492t-c2d2f7c7df2997dd415ac3ba718fa11eb3050aa6ea7cec087907a83ab36bf0433</originalsourceid><addsrcrecordid>eNp9kt1r1jAUxoMobk7_AS8k4I03mflom9YL4eV1fsBAcOptOE1P-2a2SU1awf31Znvn5kQkHBKS3_MkJzyEPBX8WHCuXyYhpCwYlyqXkCW7uEcORaklazgX9_OaF5zl4gfkUUrneVNUqnxIDlSlRcFFcUjGN5jc4Gno6W6zPZGshYQdTROMI51xXlyH1Pmda90SYqIwgPNpoWl235DOMSzortRnm09nbBu-MvmKArVhmtcFFhc8jBTmDILdPSYPehgTPrmej8iXtyeft-_Z6cd3H7abU2aLRi7Myk722uqul02ju64QJVjVghZ1D0Jgq3jJASoEbdHyWjdcQ62gVVXb80KpI_J67zuv7YSdRb9EGM0c3QTxpwngzN0T73ZmCD9MU-tS6zIbvLg2iOH7imkxk0sWxxE8hjUZqbXgdVVLkdHnf6HnYY2560zVldZVnd93Sw0wonG-D_lee2lqNrqqCiULXWfq-B9UHh1OzgaPvcv7dwRyL7AxpBSxv-lRcHOZEbPPiMkZMVcZMRdZ9OzP37mR_A5FBtQeSPnIDxhvW_qP7S-mX8bd</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2867768879</pqid></control><display><type>article</type><title>Design of hACE2-based small peptide inhibitors against spike protein of SARS-CoV-2: a computational approach</title><source>SpringerLink Journals - AutoHoldings</source><creator>Dhingra, Naveen ; Bhardwaj, Ravindra ; Bhardwaj, Uma ; Kapoor, Kapish</creator><creatorcontrib>Dhingra, Naveen ; Bhardwaj, Ravindra ; Bhardwaj, Uma ; Kapoor, Kapish</creatorcontrib><description>COVID-19 which is caused by the severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) has been declared pandemic in 2019. Though there is development of vaccines but there is an emergence requirement of drugs against SARS-CoV-2. Antiviral peptides can be rationally created and improved based on the known structures of viral proteins and their biological targets. In the given study, small peptide inhibitors with three amino acids are designed and docked against SARS-CoV-2 coronavirus using molecular docking approach. All the designed peptides bind at the active site but the highest binding affinity was observed for HisGluAsp. Molecular dynamics was performed to validate the stability and interactions of compound. The molecule has followed the druglikeness properties and with highest probability of being absorbed by the gastrointestinal tract. The results of the current investigation point to the possibility that the identified small peptides may prevent SARS-CoV-2 infection, although additional wet-lab tests are still required to confirm these results.</description><identifier>ISSN: 1040-0400</identifier><identifier>EISSN: 1572-9001</identifier><identifier>DOI: 10.1007/s11224-023-02125-z</identifier><identifier>PMID: 36714014</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Amino acids ; Antiviral agents ; Chemistry ; Chemistry and Materials Science ; Computer Applications in Chemistry ; Coronaviruses ; Dynamic stability ; Epidemics ; Gastrointestinal system ; Health aspects ; Inhibitors ; Laboratory tests ; Molecular docking ; Molecular dynamics ; Original Research ; Peptides ; Physical Chemistry ; Proteins ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Theoretical and Computational Chemistry ; Vaccines ; Viral diseases ; Viral proteins</subject><ispartof>Structural chemistry, 2023-10, Vol.34 (5), p.1843-1856</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>COPYRIGHT 2023 Springer</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c492t-c2d2f7c7df2997dd415ac3ba718fa11eb3050aa6ea7cec087907a83ab36bf0433</cites><orcidid>0000-0001-6331-8057</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11224-023-02125-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11224-023-02125-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36714014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dhingra, Naveen</creatorcontrib><creatorcontrib>Bhardwaj, Ravindra</creatorcontrib><creatorcontrib>Bhardwaj, Uma</creatorcontrib><creatorcontrib>Kapoor, Kapish</creatorcontrib><title>Design of hACE2-based small peptide inhibitors against spike protein of SARS-CoV-2: a computational approach</title><title>Structural chemistry</title><addtitle>Struct Chem</addtitle><addtitle>Struct Chem</addtitle><description>COVID-19 which is caused by the severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) has been declared pandemic in 2019. Though there is development of vaccines but there is an emergence requirement of drugs against SARS-CoV-2. Antiviral peptides can be rationally created and improved based on the known structures of viral proteins and their biological targets. In the given study, small peptide inhibitors with three amino acids are designed and docked against SARS-CoV-2 coronavirus using molecular docking approach. All the designed peptides bind at the active site but the highest binding affinity was observed for HisGluAsp. Molecular dynamics was performed to validate the stability and interactions of compound. The molecule has followed the druglikeness properties and with highest probability of being absorbed by the gastrointestinal tract. The results of the current investigation point to the possibility that the identified small peptides may prevent SARS-CoV-2 infection, although additional wet-lab tests are still required to confirm these results.</description><subject>Amino acids</subject><subject>Antiviral agents</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Computer Applications in Chemistry</subject><subject>Coronaviruses</subject><subject>Dynamic stability</subject><subject>Epidemics</subject><subject>Gastrointestinal system</subject><subject>Health aspects</subject><subject>Inhibitors</subject><subject>Laboratory tests</subject><subject>Molecular docking</subject><subject>Molecular dynamics</subject><subject>Original Research</subject><subject>Peptides</subject><subject>Physical Chemistry</subject><subject>Proteins</subject><subject>Severe acute respiratory syndrome</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Theoretical and Computational Chemistry</subject><subject>Vaccines</subject><subject>Viral diseases</subject><subject>Viral proteins</subject><issn>1040-0400</issn><issn>1572-9001</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kt1r1jAUxoMobk7_AS8k4I03mflom9YL4eV1fsBAcOptOE1P-2a2SU1awf31Znvn5kQkHBKS3_MkJzyEPBX8WHCuXyYhpCwYlyqXkCW7uEcORaklazgX9_OaF5zl4gfkUUrneVNUqnxIDlSlRcFFcUjGN5jc4Gno6W6zPZGshYQdTROMI51xXlyH1Pmda90SYqIwgPNpoWl235DOMSzortRnm09nbBu-MvmKArVhmtcFFhc8jBTmDILdPSYPehgTPrmej8iXtyeft-_Z6cd3H7abU2aLRi7Myk722uqul02ju64QJVjVghZ1D0Jgq3jJASoEbdHyWjdcQ62gVVXb80KpI_J67zuv7YSdRb9EGM0c3QTxpwngzN0T73ZmCD9MU-tS6zIbvLg2iOH7imkxk0sWxxE8hjUZqbXgdVVLkdHnf6HnYY2560zVldZVnd93Sw0wonG-D_lee2lqNrqqCiULXWfq-B9UHh1OzgaPvcv7dwRyL7AxpBSxv-lRcHOZEbPPiMkZMVcZMRdZ9OzP37mR_A5FBtQeSPnIDxhvW_qP7S-mX8bd</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Dhingra, Naveen</creator><creator>Bhardwaj, Ravindra</creator><creator>Bhardwaj, Uma</creator><creator>Kapoor, Kapish</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6331-8057</orcidid></search><sort><creationdate>20231001</creationdate><title>Design of hACE2-based small peptide inhibitors against spike protein of SARS-CoV-2: a computational approach</title><author>Dhingra, Naveen ; Bhardwaj, Ravindra ; Bhardwaj, Uma ; Kapoor, Kapish</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c492t-c2d2f7c7df2997dd415ac3ba718fa11eb3050aa6ea7cec087907a83ab36bf0433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amino acids</topic><topic>Antiviral agents</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Computer Applications in Chemistry</topic><topic>Coronaviruses</topic><topic>Dynamic stability</topic><topic>Epidemics</topic><topic>Gastrointestinal system</topic><topic>Health aspects</topic><topic>Inhibitors</topic><topic>Laboratory tests</topic><topic>Molecular docking</topic><topic>Molecular dynamics</topic><topic>Original Research</topic><topic>Peptides</topic><topic>Physical Chemistry</topic><topic>Proteins</topic><topic>Severe acute respiratory syndrome</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Theoretical and Computational Chemistry</topic><topic>Vaccines</topic><topic>Viral diseases</topic><topic>Viral proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dhingra, Naveen</creatorcontrib><creatorcontrib>Bhardwaj, Ravindra</creatorcontrib><creatorcontrib>Bhardwaj, Uma</creatorcontrib><creatorcontrib>Kapoor, Kapish</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Structural chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dhingra, Naveen</au><au>Bhardwaj, Ravindra</au><au>Bhardwaj, Uma</au><au>Kapoor, Kapish</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design of hACE2-based small peptide inhibitors against spike protein of SARS-CoV-2: a computational approach</atitle><jtitle>Structural chemistry</jtitle><stitle>Struct Chem</stitle><addtitle>Struct Chem</addtitle><date>2023-10-01</date><risdate>2023</risdate><volume>34</volume><issue>5</issue><spage>1843</spage><epage>1856</epage><pages>1843-1856</pages><issn>1040-0400</issn><eissn>1572-9001</eissn><abstract>COVID-19 which is caused by the severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) has been declared pandemic in 2019. Though there is development of vaccines but there is an emergence requirement of drugs against SARS-CoV-2. Antiviral peptides can be rationally created and improved based on the known structures of viral proteins and their biological targets. In the given study, small peptide inhibitors with three amino acids are designed and docked against SARS-CoV-2 coronavirus using molecular docking approach. All the designed peptides bind at the active site but the highest binding affinity was observed for HisGluAsp. Molecular dynamics was performed to validate the stability and interactions of compound. The molecule has followed the druglikeness properties and with highest probability of being absorbed by the gastrointestinal tract. The results of the current investigation point to the possibility that the identified small peptides may prevent SARS-CoV-2 infection, although additional wet-lab tests are still required to confirm these results.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>36714014</pmid><doi>10.1007/s11224-023-02125-z</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-6331-8057</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1040-0400
ispartof Structural chemistry, 2023-10, Vol.34 (5), p.1843-1856
issn 1040-0400
1572-9001
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9875775
source SpringerLink Journals - AutoHoldings
subjects Amino acids
Antiviral agents
Chemistry
Chemistry and Materials Science
Computer Applications in Chemistry
Coronaviruses
Dynamic stability
Epidemics
Gastrointestinal system
Health aspects
Inhibitors
Laboratory tests
Molecular docking
Molecular dynamics
Original Research
Peptides
Physical Chemistry
Proteins
Severe acute respiratory syndrome
Severe acute respiratory syndrome coronavirus 2
Theoretical and Computational Chemistry
Vaccines
Viral diseases
Viral proteins
title Design of hACE2-based small peptide inhibitors against spike protein of SARS-CoV-2: a computational approach
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T23%3A40%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Design%20of%20hACE2-based%20small%20peptide%20inhibitors%20against%20spike%20protein%20of%20SARS-CoV-2:%20a%20computational%20approach&rft.jtitle=Structural%20chemistry&rft.au=Dhingra,%20Naveen&rft.date=2023-10-01&rft.volume=34&rft.issue=5&rft.spage=1843&rft.epage=1856&rft.pages=1843-1856&rft.issn=1040-0400&rft.eissn=1572-9001&rft_id=info:doi/10.1007/s11224-023-02125-z&rft_dat=%3Cgale_pubme%3EA766432478%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2867768879&rft_id=info:pmid/36714014&rft_galeid=A766432478&rfr_iscdi=true