The crystal structure of the Hazara virus nucleocapsid protein
Hazara virus (HAZV) is a member of the Bunyaviridae family of segmented negative stranded RNA viruses, and shares the same serogroup as Crimean-Congo haemorrhagic fever virus (CCHFV). CCHFV is responsible for fatal human disease with a mortality rate approaching 30 %, which has an increased recent i...
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description | Hazara virus (HAZV) is a member of the Bunyaviridae family of segmented negative stranded RNA viruses, and shares the same serogroup as Crimean-Congo haemorrhagic fever virus (CCHFV). CCHFV is responsible for fatal human disease with a mortality rate approaching 30 %, which has an increased recent incidence within southern Europe. There are no preventative or therapeutic treatments for CCHFV-mediated disease, and thus CCHFV is classified as a hazard group 4 pathogen. In contrast HAZV is not associated with serious human disease, although infection of interferon receptor knockout mice with either CCHFV or HAZV results in similar disease progression. To characterise further similarities between HAZV and CCHFV, and support the use of HAZV as a model for CCHFV infection, we investigated the structure of the HAZV nucleocapsid protein (N) and compared it to CCHFV N. N performs an essential role in the viral life cycle by encapsidating the viral RNA genome, and thus, N represents a potential therapeutic target.
We present the purification, crystallisation and crystal structure of HAZV N at 2.7 Å resolution. HAZV N was expressed as an N-terminal glutathione S-transferase (GST) fusion protein then purified using glutathione affinity chromatography followed by ion-exchange chromatography. HAZV N crystallised in the P212121 space group with unit cell parameters a = 64.99, b = 76.10, and c = 449.28 Å. HAZV N consists of a globular domain formed mostly of alpha helices derived from both the N- and C-termini, and an arm domain comprising two long alpha helices. HAZV N has a similar overall structure to CCHFV N, with their globular domains superposing with an RMSD = 0.70 Å, over 368 alpha carbons that share 59 % sequence identity. Four HAZV N monomers crystallised in the asymmetric unit, and their head-to-tail assembly reveals a potential interaction site between monomers.
The crystal structure of HAZV N reveals a close similarity to CCHFV N, supporting the use of HAZV as a model for CCHFV. Structural similarity between the N proteins should facilitate study of the CCHFV and HAZV replication cycles without the necessity of working under containment level 4 (CL-4) conditions. |
doi_str_mv | 10.1186/s12900-015-0051-3 |
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We present the purification, crystallisation and crystal structure of HAZV N at 2.7 Å resolution. HAZV N was expressed as an N-terminal glutathione S-transferase (GST) fusion protein then purified using glutathione affinity chromatography followed by ion-exchange chromatography. HAZV N crystallised in the P212121 space group with unit cell parameters a = 64.99, b = 76.10, and c = 449.28 Å. HAZV N consists of a globular domain formed mostly of alpha helices derived from both the N- and C-termini, and an arm domain comprising two long alpha helices. HAZV N has a similar overall structure to CCHFV N, with their globular domains superposing with an RMSD = 0.70 Å, over 368 alpha carbons that share 59 % sequence identity. Four HAZV N monomers crystallised in the asymmetric unit, and their head-to-tail assembly reveals a potential interaction site between monomers.
The crystal structure of HAZV N reveals a close similarity to CCHFV N, supporting the use of HAZV as a model for CCHFV. Structural similarity between the N proteins should facilitate study of the CCHFV and HAZV replication cycles without the necessity of working under containment level 4 (CL-4) conditions.</description><identifier>ISSN: 1472-6807</identifier><identifier>EISSN: 1472-6807</identifier><identifier>DOI: 10.1186/s12900-015-0051-3</identifier><identifier>PMID: 26715309</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Amino Acid Sequence ; Analysis ; Care and treatment ; Complications and side effects ; Crystallography, X-Ray ; Crystals ; Health aspects ; Hemorrhagic fever ; Humans ; Interferon ; Models, Molecular ; Molecular Sequence Data ; Nairovirus ; Nucleocapsid Proteins - chemistry ; Nucleocapsid Proteins - genetics ; Nucleocapsid Proteins - isolation & purification ; Nucleocapsid Proteins - metabolism ; Protein Structure, Secondary ; Static Electricity ; Structure</subject><ispartof>BMC structural biology, 2015-12, Vol.15 (24), p.24-24, Article 24</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Surtees et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-22e4db07fcc830dba2453cb3c1cae6c561cba3832f3374275979428a8f131aac3</citedby><cites>FETCH-LOGICAL-c594t-22e4db07fcc830dba2453cb3c1cae6c561cba3832f3374275979428a8f131aac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696240/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696240/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26715309$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Surtees, Rebecca</creatorcontrib><creatorcontrib>Ariza, Antonio</creatorcontrib><creatorcontrib>Punch, Emma K</creatorcontrib><creatorcontrib>Trinh, Chi H</creatorcontrib><creatorcontrib>Dowall, Stuart D</creatorcontrib><creatorcontrib>Hewson, Roger</creatorcontrib><creatorcontrib>Hiscox, Julian A</creatorcontrib><creatorcontrib>Barr, John N</creatorcontrib><creatorcontrib>Edwards, Thomas A</creatorcontrib><title>The crystal structure of the Hazara virus nucleocapsid protein</title><title>BMC structural biology</title><addtitle>BMC Struct Biol</addtitle><description>Hazara virus (HAZV) is a member of the Bunyaviridae family of segmented negative stranded RNA viruses, and shares the same serogroup as Crimean-Congo haemorrhagic fever virus (CCHFV). CCHFV is responsible for fatal human disease with a mortality rate approaching 30 %, which has an increased recent incidence within southern Europe. There are no preventative or therapeutic treatments for CCHFV-mediated disease, and thus CCHFV is classified as a hazard group 4 pathogen. In contrast HAZV is not associated with serious human disease, although infection of interferon receptor knockout mice with either CCHFV or HAZV results in similar disease progression. To characterise further similarities between HAZV and CCHFV, and support the use of HAZV as a model for CCHFV infection, we investigated the structure of the HAZV nucleocapsid protein (N) and compared it to CCHFV N. N performs an essential role in the viral life cycle by encapsidating the viral RNA genome, and thus, N represents a potential therapeutic target.
We present the purification, crystallisation and crystal structure of HAZV N at 2.7 Å resolution. HAZV N was expressed as an N-terminal glutathione S-transferase (GST) fusion protein then purified using glutathione affinity chromatography followed by ion-exchange chromatography. HAZV N crystallised in the P212121 space group with unit cell parameters a = 64.99, b = 76.10, and c = 449.28 Å. HAZV N consists of a globular domain formed mostly of alpha helices derived from both the N- and C-termini, and an arm domain comprising two long alpha helices. HAZV N has a similar overall structure to CCHFV N, with their globular domains superposing with an RMSD = 0.70 Å, over 368 alpha carbons that share 59 % sequence identity. Four HAZV N monomers crystallised in the asymmetric unit, and their head-to-tail assembly reveals a potential interaction site between monomers.
The crystal structure of HAZV N reveals a close similarity to CCHFV N, supporting the use of HAZV as a model for CCHFV. Structural similarity between the N proteins should facilitate study of the CCHFV and HAZV replication cycles without the necessity of working under containment level 4 (CL-4) conditions.</description><subject>Amino Acid Sequence</subject><subject>Analysis</subject><subject>Care and treatment</subject><subject>Complications and side effects</subject><subject>Crystallography, X-Ray</subject><subject>Crystals</subject><subject>Health aspects</subject><subject>Hemorrhagic fever</subject><subject>Humans</subject><subject>Interferon</subject><subject>Models, Molecular</subject><subject>Molecular Sequence Data</subject><subject>Nairovirus</subject><subject>Nucleocapsid Proteins - chemistry</subject><subject>Nucleocapsid Proteins - genetics</subject><subject>Nucleocapsid Proteins - isolation & purification</subject><subject>Nucleocapsid Proteins - metabolism</subject><subject>Protein Structure, Secondary</subject><subject>Static Electricity</subject><subject>Structure</subject><issn>1472-6807</issn><issn>1472-6807</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptks1rFTEUxQdRbK3-AW5kwI0upubmYzKzKZSitlAQtK7DnTuZ15R5k2c-ivWvN49Xa59IFgm5v3NCDqeqXgM7BujaDxF4z1jDQDWMKWjEk-oQpOZN2zH99NH5oHoR4w1joDsln1cHvNWgBOsPq5Ora1tTuIsJ5zqmkCnlYGs_1akMzvEXBqxvXcixXjLN1hNuohvrTfDJuuVl9WzCOdpX9_tR9f3Tx6uz8-byy-eLs9PLhlQvU8O5lePA9ETUCTYOyKUSNAgCQtuSaoEGFJ3gkxBacq163UveYTeBAEQSR9XJzneTh7UdyS4p4Gw2wa0x3BmPzuxPFndtVv7WyLZvuWTF4N29QfA_so3JrF0kO8-4WJ-jAa247jTnqqBv_0FvfA5L-V6hdK-01gr-UiucrXHL5Mu7tDU1p1JBCZgBL9Txf6iyRrt25Bc7uXK_J3i_JyhMsj_TCnOM5uLb130WdiwFH2Ow00MewMy2IGZXEFMKYrYFMaJo3jwO8kHxpxHiN04us9I</recordid><startdate>20151229</startdate><enddate>20151229</enddate><creator>Surtees, Rebecca</creator><creator>Ariza, Antonio</creator><creator>Punch, Emma K</creator><creator>Trinh, Chi H</creator><creator>Dowall, Stuart D</creator><creator>Hewson, Roger</creator><creator>Hiscox, Julian A</creator><creator>Barr, John N</creator><creator>Edwards, Thomas A</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><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>ISR</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151229</creationdate><title>The crystal structure of the Hazara virus nucleocapsid protein</title><author>Surtees, Rebecca ; Ariza, Antonio ; Punch, Emma K ; Trinh, Chi H ; Dowall, Stuart D ; Hewson, Roger ; Hiscox, Julian A ; Barr, John N ; Edwards, Thomas A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-22e4db07fcc830dba2453cb3c1cae6c561cba3832f3374275979428a8f131aac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Amino Acid Sequence</topic><topic>Analysis</topic><topic>Care and treatment</topic><topic>Complications and side effects</topic><topic>Crystallography, X-Ray</topic><topic>Crystals</topic><topic>Health aspects</topic><topic>Hemorrhagic fever</topic><topic>Humans</topic><topic>Interferon</topic><topic>Models, Molecular</topic><topic>Molecular Sequence Data</topic><topic>Nairovirus</topic><topic>Nucleocapsid Proteins - chemistry</topic><topic>Nucleocapsid Proteins - genetics</topic><topic>Nucleocapsid Proteins - isolation & purification</topic><topic>Nucleocapsid Proteins - metabolism</topic><topic>Protein Structure, Secondary</topic><topic>Static Electricity</topic><topic>Structure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Surtees, Rebecca</creatorcontrib><creatorcontrib>Ariza, Antonio</creatorcontrib><creatorcontrib>Punch, Emma K</creatorcontrib><creatorcontrib>Trinh, Chi H</creatorcontrib><creatorcontrib>Dowall, Stuart D</creatorcontrib><creatorcontrib>Hewson, Roger</creatorcontrib><creatorcontrib>Hiscox, Julian A</creatorcontrib><creatorcontrib>Barr, John N</creatorcontrib><creatorcontrib>Edwards, Thomas A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC structural biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Surtees, Rebecca</au><au>Ariza, Antonio</au><au>Punch, Emma K</au><au>Trinh, Chi H</au><au>Dowall, Stuart D</au><au>Hewson, Roger</au><au>Hiscox, Julian A</au><au>Barr, John N</au><au>Edwards, Thomas A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The crystal structure of the Hazara virus nucleocapsid protein</atitle><jtitle>BMC structural biology</jtitle><addtitle>BMC Struct Biol</addtitle><date>2015-12-29</date><risdate>2015</risdate><volume>15</volume><issue>24</issue><spage>24</spage><epage>24</epage><pages>24-24</pages><artnum>24</artnum><issn>1472-6807</issn><eissn>1472-6807</eissn><abstract>Hazara virus (HAZV) is a member of the Bunyaviridae family of segmented negative stranded RNA viruses, and shares the same serogroup as Crimean-Congo haemorrhagic fever virus (CCHFV). CCHFV is responsible for fatal human disease with a mortality rate approaching 30 %, which has an increased recent incidence within southern Europe. There are no preventative or therapeutic treatments for CCHFV-mediated disease, and thus CCHFV is classified as a hazard group 4 pathogen. In contrast HAZV is not associated with serious human disease, although infection of interferon receptor knockout mice with either CCHFV or HAZV results in similar disease progression. To characterise further similarities between HAZV and CCHFV, and support the use of HAZV as a model for CCHFV infection, we investigated the structure of the HAZV nucleocapsid protein (N) and compared it to CCHFV N. N performs an essential role in the viral life cycle by encapsidating the viral RNA genome, and thus, N represents a potential therapeutic target.
We present the purification, crystallisation and crystal structure of HAZV N at 2.7 Å resolution. HAZV N was expressed as an N-terminal glutathione S-transferase (GST) fusion protein then purified using glutathione affinity chromatography followed by ion-exchange chromatography. HAZV N crystallised in the P212121 space group with unit cell parameters a = 64.99, b = 76.10, and c = 449.28 Å. HAZV N consists of a globular domain formed mostly of alpha helices derived from both the N- and C-termini, and an arm domain comprising two long alpha helices. HAZV N has a similar overall structure to CCHFV N, with their globular domains superposing with an RMSD = 0.70 Å, over 368 alpha carbons that share 59 % sequence identity. Four HAZV N monomers crystallised in the asymmetric unit, and their head-to-tail assembly reveals a potential interaction site between monomers.
The crystal structure of HAZV N reveals a close similarity to CCHFV N, supporting the use of HAZV as a model for CCHFV. Structural similarity between the N proteins should facilitate study of the CCHFV and HAZV replication cycles without the necessity of working under containment level 4 (CL-4) conditions.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26715309</pmid><doi>10.1186/s12900-015-0051-3</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Analysis Care and treatment Complications and side effects Crystallography, X-Ray Crystals Health aspects Hemorrhagic fever Humans Interferon Models, Molecular Molecular Sequence Data Nairovirus Nucleocapsid Proteins - chemistry Nucleocapsid Proteins - genetics Nucleocapsid Proteins - isolation & purification Nucleocapsid Proteins - metabolism Protein Structure, Secondary Static Electricity Structure |
title | The crystal structure of the Hazara virus nucleocapsid protein |
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