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In Silico Structural and Functional Analyses of NLRP3 Inflammasomes to Provide Insights for Treating Neurodegenerative Diseases
Inflammasomes are cytoplasmic intracellular multiprotein complexes that control the innate immune system’s activation of inflammation in response to derived chemicals. Recent advancements increased our molecular knowledge of activation of NLRP3 inflammasomes. Although several studies have been done...
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Published in: | BioMed research international 2023, Vol.2023 (1), p.9819005-9819005 |
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creator | Ghazi, Behram Khan Bangash, Maria Hussain Razzaq, Anam Abdul Kiyani, Madiha Girmay, Shishay Chaudhary, Waleed Razzaq Zahid, Usman Hussain, Uzma Mujahid, Huma Parvaiz, Usama Buzdar, Irfan Ahmed Nawaz, Shah Elsadek, Mohamed Farouk |
description | Inflammasomes are cytoplasmic intracellular multiprotein complexes that control the innate immune system’s activation of inflammation in response to derived chemicals. Recent advancements increased our molecular knowledge of activation of NLRP3 inflammasomes. Although several studies have been done to investigate the role of inflammasomes in innate immunity and other diseases, structural, functional, and evolutionary investigations are needed to further understand the clinical consequences of NLRP3 gene. The purpose of this study is to investigate the structural and functional impact of the NLRP3 protein by using a computational analysis to uncover putative protein sites involved in the stabilization of the protein-ligand complexes with inhibitors. This will allow for a deeper understanding of the molecular mechanism underlying these interactions. It was found that human NLRP3 gene coexpresses with PYCARD, NLRC4, CASP1, MAVS, and CTSB based on observed coexpression of homologs in other species. The NACHT, LRR, and PYD domain-containing protein 3 is a key player in innate immunity and inflammation as the sensor subunit of the NLRP3 inflammasome. The inflammasome polymeric complex, consisting of NLRP3, PYCARD, and CASP1, is formed in response to pathogens and other damage-associated signals (and possibly CASP4 and CASP5). Comprehensive structural and functional analyses of NLRP3 inflammasome components offer a fresh approach to the development of new treatments for a wide variety of human disorders. |
doi_str_mv | 10.1155/2023/9819005 |
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Recent advancements increased our molecular knowledge of activation of NLRP3 inflammasomes. Although several studies have been done to investigate the role of inflammasomes in innate immunity and other diseases, structural, functional, and evolutionary investigations are needed to further understand the clinical consequences of NLRP3 gene. The purpose of this study is to investigate the structural and functional impact of the NLRP3 protein by using a computational analysis to uncover putative protein sites involved in the stabilization of the protein-ligand complexes with inhibitors. This will allow for a deeper understanding of the molecular mechanism underlying these interactions. It was found that human NLRP3 gene coexpresses with PYCARD, NLRC4, CASP1, MAVS, and CTSB based on observed coexpression of homologs in other species. The NACHT, LRR, and PYD domain-containing protein 3 is a key player in innate immunity and inflammation as the sensor subunit of the NLRP3 inflammasome. The inflammasome polymeric complex, consisting of NLRP3, PYCARD, and CASP1, is formed in response to pathogens and other damage-associated signals (and possibly CASP4 and CASP5). Comprehensive structural and functional analyses of NLRP3 inflammasome components offer a fresh approach to the development of new treatments for a wide variety of human disorders.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2023/9819005</identifier><identifier>PMID: 36726838</identifier><language>eng</language><publisher>United States: Hindawi</publisher><subject>Alzheimer's disease ; Binding sites ; Caspase 1 - metabolism ; Cytokines ; Degeneration ; Humans ; Immune system ; Immunity ; Immunity, Innate ; Inflammasomes ; Inflammasomes - metabolism ; Inflammation ; Inflammation - genetics ; Innate immunity ; Ligands ; Nervous system ; Neurodegenerative diseases ; Neurodegenerative Diseases - genetics ; NLR Family, Pyrin Domain-Containing 3 Protein - genetics ; NLR Family, Pyrin Domain-Containing 3 Protein - metabolism ; Proteins ; Software ; Structure-function relationships</subject><ispartof>BioMed research international, 2023, Vol.2023 (1), p.9819005-9819005</ispartof><rights>Copyright © 2023 Behram Khan Ghazi et al.</rights><rights>COPYRIGHT 2023 John Wiley & Sons, Inc.</rights><rights>Copyright © 2023 Behram Khan Ghazi et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2023 Behram Khan Ghazi et al. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-3014c6773957df6106e8bd34865035fde33457bc2a9fee4f8ab434fcbced35a53</citedby><cites>FETCH-LOGICAL-c476t-3014c6773957df6106e8bd34865035fde33457bc2a9fee4f8ab434fcbced35a53</cites><orcidid>0000-0002-5318-4902 ; 0000-0001-6180-0384</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2772878635/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2772878635?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,4024,25753,27923,27924,27925,37012,37013,44590,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36726838$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Shah, Shahid Ali</contributor><contributor>Shahid Ali Shah</contributor><creatorcontrib>Ghazi, Behram Khan</creatorcontrib><creatorcontrib>Bangash, Maria Hussain</creatorcontrib><creatorcontrib>Razzaq, Anam Abdul</creatorcontrib><creatorcontrib>Kiyani, Madiha</creatorcontrib><creatorcontrib>Girmay, Shishay</creatorcontrib><creatorcontrib>Chaudhary, Waleed Razzaq</creatorcontrib><creatorcontrib>Zahid, Usman</creatorcontrib><creatorcontrib>Hussain, Uzma</creatorcontrib><creatorcontrib>Mujahid, Huma</creatorcontrib><creatorcontrib>Parvaiz, Usama</creatorcontrib><creatorcontrib>Buzdar, Irfan Ahmed</creatorcontrib><creatorcontrib>Nawaz, Shah</creatorcontrib><creatorcontrib>Elsadek, Mohamed Farouk</creatorcontrib><title>In Silico Structural and Functional Analyses of NLRP3 Inflammasomes to Provide Insights for Treating Neurodegenerative Diseases</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Inflammasomes are cytoplasmic intracellular multiprotein complexes that control the innate immune system’s activation of inflammation in response to derived chemicals. Recent advancements increased our molecular knowledge of activation of NLRP3 inflammasomes. Although several studies have been done to investigate the role of inflammasomes in innate immunity and other diseases, structural, functional, and evolutionary investigations are needed to further understand the clinical consequences of NLRP3 gene. The purpose of this study is to investigate the structural and functional impact of the NLRP3 protein by using a computational analysis to uncover putative protein sites involved in the stabilization of the protein-ligand complexes with inhibitors. This will allow for a deeper understanding of the molecular mechanism underlying these interactions. It was found that human NLRP3 gene coexpresses with PYCARD, NLRC4, CASP1, MAVS, and CTSB based on observed coexpression of homologs in other species. The NACHT, LRR, and PYD domain-containing protein 3 is a key player in innate immunity and inflammation as the sensor subunit of the NLRP3 inflammasome. The inflammasome polymeric complex, consisting of NLRP3, PYCARD, and CASP1, is formed in response to pathogens and other damage-associated signals (and possibly CASP4 and CASP5). Comprehensive structural and functional analyses of NLRP3 inflammasome components offer a fresh approach to the development of new treatments for a wide variety of human disorders.</description><subject>Alzheimer's disease</subject><subject>Binding sites</subject><subject>Caspase 1 - metabolism</subject><subject>Cytokines</subject><subject>Degeneration</subject><subject>Humans</subject><subject>Immune system</subject><subject>Immunity</subject><subject>Immunity, Innate</subject><subject>Inflammasomes</subject><subject>Inflammasomes - metabolism</subject><subject>Inflammation</subject><subject>Inflammation - genetics</subject><subject>Innate immunity</subject><subject>Ligands</subject><subject>Nervous system</subject><subject>Neurodegenerative diseases</subject><subject>Neurodegenerative Diseases - genetics</subject><subject>NLR Family, Pyrin Domain-Containing 3 Protein - genetics</subject><subject>NLR Family, Pyrin Domain-Containing 3 Protein - metabolism</subject><subject>Proteins</subject><subject>Software</subject><subject>Structure-function relationships</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9kktvEzEQgFcIRKvSG2dkiQsShNrr516QokIhUlQqWs6W1ztOXO3arb0b1BN_HYeE8Djggx_jT5899lTVc4LfEsL5WY1retYo0mDMH1XHNSVsJggjjw9zSo-q05xvcWmKCNyIp9URFbIWiqrj6vsioGvfexvR9ZgmO07J9MiEDl1MwY4-hrKcl-4hQ0bRocvllyuKFsH1ZhhMjkMJjxFdpbjxHZSN7FfrMSMXE7pJYEYfVugSphQ7WEGAVCIbQO99BlOUz6onzvQZTvfjSfX14sPN-afZ8vPHxfl8ObNMinFGMWFWSEkbLjsnCBag2o4yJTim3HVAKeOytbVpHABzyrSMMmdbCx3lhtOT6t3Oeze1A3QWwlgS1XfJDyY96Gi8_nsn-LVexY1ulBJM1EXwai9I8X6CPOrBZwt9bwLEKetaStIwXDeioC__QW_jlMob_qRqJZWg_De1Mj1oH1ws59qtVM8l5U1Dqdi63uwom2LOCdzhygTrbQnobQnofQkU_MWfaR7gXx9egNc7YO1DZ775_-t-AIOJuTY</recordid><startdate>2023</startdate><enddate>2023</enddate><creator>Ghazi, Behram Khan</creator><creator>Bangash, Maria Hussain</creator><creator>Razzaq, Anam Abdul</creator><creator>Kiyani, Madiha</creator><creator>Girmay, Shishay</creator><creator>Chaudhary, Waleed Razzaq</creator><creator>Zahid, Usman</creator><creator>Hussain, Uzma</creator><creator>Mujahid, Huma</creator><creator>Parvaiz, Usama</creator><creator>Buzdar, Irfan Ahmed</creator><creator>Nawaz, Shah</creator><creator>Elsadek, Mohamed Farouk</creator><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5318-4902</orcidid><orcidid>https://orcid.org/0000-0001-6180-0384</orcidid></search><sort><creationdate>2023</creationdate><title>In Silico Structural and Functional Analyses of NLRP3 Inflammasomes to Provide Insights for Treating Neurodegenerative Diseases</title><author>Ghazi, Behram Khan ; Bangash, Maria Hussain ; Razzaq, Anam Abdul ; Kiyani, Madiha ; Girmay, Shishay ; Chaudhary, Waleed Razzaq ; Zahid, Usman ; Hussain, Uzma ; Mujahid, Huma ; Parvaiz, Usama ; Buzdar, Irfan Ahmed ; Nawaz, Shah ; Elsadek, Mohamed Farouk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-3014c6773957df6106e8bd34865035fde33457bc2a9fee4f8ab434fcbced35a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alzheimer's disease</topic><topic>Binding sites</topic><topic>Caspase 1 - 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Recent advancements increased our molecular knowledge of activation of NLRP3 inflammasomes. Although several studies have been done to investigate the role of inflammasomes in innate immunity and other diseases, structural, functional, and evolutionary investigations are needed to further understand the clinical consequences of NLRP3 gene. The purpose of this study is to investigate the structural and functional impact of the NLRP3 protein by using a computational analysis to uncover putative protein sites involved in the stabilization of the protein-ligand complexes with inhibitors. This will allow for a deeper understanding of the molecular mechanism underlying these interactions. It was found that human NLRP3 gene coexpresses with PYCARD, NLRC4, CASP1, MAVS, and CTSB based on observed coexpression of homologs in other species. The NACHT, LRR, and PYD domain-containing protein 3 is a key player in innate immunity and inflammation as the sensor subunit of the NLRP3 inflammasome. The inflammasome polymeric complex, consisting of NLRP3, PYCARD, and CASP1, is formed in response to pathogens and other damage-associated signals (and possibly CASP4 and CASP5). Comprehensive structural and functional analyses of NLRP3 inflammasome components offer a fresh approach to the development of new treatments for a wide variety of human disorders.</abstract><cop>United States</cop><pub>Hindawi</pub><pmid>36726838</pmid><doi>10.1155/2023/9819005</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-5318-4902</orcidid><orcidid>https://orcid.org/0000-0001-6180-0384</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer's disease Binding sites Caspase 1 - metabolism Cytokines Degeneration Humans Immune system Immunity Immunity, Innate Inflammasomes Inflammasomes - metabolism Inflammation Inflammation - genetics Innate immunity Ligands Nervous system Neurodegenerative diseases Neurodegenerative Diseases - genetics NLR Family, Pyrin Domain-Containing 3 Protein - genetics NLR Family, Pyrin Domain-Containing 3 Protein - metabolism Proteins Software Structure-function relationships |
title | In Silico Structural and Functional Analyses of NLRP3 Inflammasomes to Provide Insights for Treating Neurodegenerative Diseases |
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