Preparation of truncated orf virus entry fusion complex proteins by chemical synthesis
Members of the Chordopoxvirinae subfamily possess an unusual 11 protein entry–fusion complex (EFC) that is highly conserved and present in all species. The mode of action of this EFC is unknown, and the interactions of the constituent proteins are uncharacterised. Here, we present the chemical synth...
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Veröffentlicht in: | Journal of peptide science 2014-06, Vol.20 (6), p.398-405 |
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description | Members of the Chordopoxvirinae subfamily possess an unusual 11 protein entry–fusion complex (EFC) that is highly conserved and present in all species. The mode of action of this EFC is unknown, and the interactions of the constituent proteins are uncharacterised. Here, we present the chemical synthesis of membrane domain truncated linear constructs of two EFC proteins in orf virus, ORFV036 and 049. By using Boc solid phase peptide synthesis and native chemical ligation methods, these truncated proteins have been readily prepared in milligram quantities. These robust synthetic protocols allow ready access to these polypeptides to facilitate biological studies. Copyright © 2014 European Peptide Society and John Wiley & Sons, Ltd.
Orf virus requires an unusually large ≥11‐protein entry fusion complex to enter host cells. Through chemical synthesis, we have prepared truncated constructs of two of these entry fusion proteins (ORFV036 and 049), which were previously found to be intractable to bacterial expression. The robust synthetic protocols used allow access to milligram quantities in high purity for further biological studies. |
doi_str_mv | 10.1002/psc.2627 |
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Orf virus requires an unusually large ≥11‐protein entry fusion complex to enter host cells. Through chemical synthesis, we have prepared truncated constructs of two of these entry fusion proteins (ORFV036 and 049), which were previously found to be intractable to bacterial expression. The robust synthetic protocols used allow access to milligram quantities in high purity for further biological studies.</description><identifier>ISSN: 1075-2617</identifier><identifier>EISSN: 1099-1387</identifier><identifier>DOI: 10.1002/psc.2627</identifier><identifier>PMID: 24652714</identifier><identifier>CODEN: JPSIEI</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Chordopoxvirinae ; chordopoxvirus ; entry fusion complex ; Molecular Structure ; native chemical ligation ; Orf virus ; Orf virus - chemistry ; Peptides ; Peptides - chemical synthesis ; Peptides - chemistry ; Viral Fusion Proteins - chemical synthesis ; Viral Fusion Proteins - chemistry</subject><ispartof>Journal of peptide science, 2014-06, Vol.20 (6), p.398-405</ispartof><rights>Copyright © 2014 European Peptide Society and John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3817-c5d71fcdd5767a83a003e26f34c85526d109011293ee749c78f5a8540d5c801b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpsc.2627$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpsc.2627$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24652714$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yeung, Ho</creatorcontrib><creatorcontrib>Harris, Paul W. R.</creatorcontrib><creatorcontrib>Squire, Christopher J.</creatorcontrib><creatorcontrib>Baker, Edward N.</creatorcontrib><creatorcontrib>Brimble, Margaret A.</creatorcontrib><title>Preparation of truncated orf virus entry fusion complex proteins by chemical synthesis</title><title>Journal of peptide science</title><addtitle>J. Pept. Sci</addtitle><description>Members of the Chordopoxvirinae subfamily possess an unusual 11 protein entry–fusion complex (EFC) that is highly conserved and present in all species. The mode of action of this EFC is unknown, and the interactions of the constituent proteins are uncharacterised. Here, we present the chemical synthesis of membrane domain truncated linear constructs of two EFC proteins in orf virus, ORFV036 and 049. By using Boc solid phase peptide synthesis and native chemical ligation methods, these truncated proteins have been readily prepared in milligram quantities. These robust synthetic protocols allow ready access to these polypeptides to facilitate biological studies. Copyright © 2014 European Peptide Society and John Wiley & Sons, Ltd.
Orf virus requires an unusually large ≥11‐protein entry fusion complex to enter host cells. Through chemical synthesis, we have prepared truncated constructs of two of these entry fusion proteins (ORFV036 and 049), which were previously found to be intractable to bacterial expression. The robust synthetic protocols used allow access to milligram quantities in high purity for further biological studies.</description><subject>Chordopoxvirinae</subject><subject>chordopoxvirus</subject><subject>entry fusion complex</subject><subject>Molecular Structure</subject><subject>native chemical ligation</subject><subject>Orf virus</subject><subject>Orf virus - chemistry</subject><subject>Peptides</subject><subject>Peptides - chemical synthesis</subject><subject>Peptides - chemistry</subject><subject>Viral Fusion Proteins - chemical synthesis</subject><subject>Viral Fusion Proteins - chemistry</subject><issn>1075-2617</issn><issn>1099-1387</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0dtKHTEUBuAgFbVW8Akk0BtvRnOYHOZSt9YWRIV6ugvZmTUYOyeTmXbP2zeDuxYKBa9WYH38ZPEjtE_JESWEHffRHTHJ1AbaoaQoMsq1-jC_lciYpGobfYzxmZC0E3ILbbNcCqZovoPubwL0NtjBdy3uKjyEsXV2gBJ3ocI_fRgjhnYIE67GOBvXNX0NK9yHbgDfRrycsHuCxjtb4zi1wxNEHz-hzcrWEfbWcxfdfTm_XXzNLq8vvi1OLjPHNVWZE6WilStLoaSymltCODBZ8dxpIZgs0zWEUlZwAJUXTulKWC1yUgqnCV3yXXT4mpu-8zJCHEzjo4O6ti10YzRUsKLIU5R-D82pIgWViX7-hz53Y2jTIbNimnBF1N9AF7oYA1SmD76xYTKUmLkWk2oxcy2JHqwDx2UD5Rv800MC2Sv45WuY_htkbr4v1oFr7-MAqzdvww8jFVfCPFxdGHb2uDh9zK_MPf8N6kOkQw</recordid><startdate>201406</startdate><enddate>201406</enddate><creator>Yeung, Ho</creator><creator>Harris, Paul W. 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R. ; Squire, Christopher J. ; Baker, Edward N. ; Brimble, Margaret A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3817-c5d71fcdd5767a83a003e26f34c85526d109011293ee749c78f5a8540d5c801b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Chordopoxvirinae</topic><topic>chordopoxvirus</topic><topic>entry fusion complex</topic><topic>Molecular Structure</topic><topic>native chemical ligation</topic><topic>Orf virus</topic><topic>Orf virus - chemistry</topic><topic>Peptides</topic><topic>Peptides - chemical synthesis</topic><topic>Peptides - chemistry</topic><topic>Viral Fusion Proteins - chemical synthesis</topic><topic>Viral Fusion Proteins - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yeung, Ho</creatorcontrib><creatorcontrib>Harris, Paul W. R.</creatorcontrib><creatorcontrib>Squire, Christopher J.</creatorcontrib><creatorcontrib>Baker, Edward N.</creatorcontrib><creatorcontrib>Brimble, Margaret A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of peptide science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yeung, Ho</au><au>Harris, Paul W. R.</au><au>Squire, Christopher J.</au><au>Baker, Edward N.</au><au>Brimble, Margaret A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of truncated orf virus entry fusion complex proteins by chemical synthesis</atitle><jtitle>Journal of peptide science</jtitle><addtitle>J. Pept. Sci</addtitle><date>2014-06</date><risdate>2014</risdate><volume>20</volume><issue>6</issue><spage>398</spage><epage>405</epage><pages>398-405</pages><issn>1075-2617</issn><eissn>1099-1387</eissn><coden>JPSIEI</coden><abstract>Members of the Chordopoxvirinae subfamily possess an unusual 11 protein entry–fusion complex (EFC) that is highly conserved and present in all species. The mode of action of this EFC is unknown, and the interactions of the constituent proteins are uncharacterised. Here, we present the chemical synthesis of membrane domain truncated linear constructs of two EFC proteins in orf virus, ORFV036 and 049. By using Boc solid phase peptide synthesis and native chemical ligation methods, these truncated proteins have been readily prepared in milligram quantities. These robust synthetic protocols allow ready access to these polypeptides to facilitate biological studies. Copyright © 2014 European Peptide Society and John Wiley & Sons, Ltd.
Orf virus requires an unusually large ≥11‐protein entry fusion complex to enter host cells. Through chemical synthesis, we have prepared truncated constructs of two of these entry fusion proteins (ORFV036 and 049), which were previously found to be intractable to bacterial expression. The robust synthetic protocols used allow access to milligram quantities in high purity for further biological studies.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24652714</pmid><doi>10.1002/psc.2627</doi><tpages>8</tpages></addata></record> |
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subjects | Chordopoxvirinae chordopoxvirus entry fusion complex Molecular Structure native chemical ligation Orf virus Orf virus - chemistry Peptides Peptides - chemical synthesis Peptides - chemistry Viral Fusion Proteins - chemical synthesis Viral Fusion Proteins - chemistry |
title | Preparation of truncated orf virus entry fusion complex proteins by chemical synthesis |
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