VP24

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m (Sandbox VP24 Clark Wilson moved to VP24: original Sandbox by Clark Wilson)
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==VP24==
==VP24==
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<StructureSection load='4D9O' size='340' side='right' caption='VP24 from the Reston Ebola Virus' scene=''>
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<StructureSection load='4d9o' size='340' side='right' caption='VP24 from the Reston Ebola Virus [[4d9o]]' scene=''>
== Introduction ==
== Introduction ==
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VP24 is a protein present in the Ebola and Marburg viruses, both of which are members of ''Filoviridae'' family. Presently there are five strains of Ebola: Sudan, Reston, Zaire, Bundibugyo, and Taï Forest, each with minor differences in VP24 sequences(1).
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VP24 is a protein present in the Ebola and Marburg viruses, both of which are members of ''Filoviridae'' family. Presently there are five strains of Ebola: Sudan, Reston, Zaire, Bundibugyo, and Taï Forest, each with minor differences in VP24 sequences <ref name='24574400 '>pmid 24574400</ref>.
== Function ==
== Function ==
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'''Ebola'''
'''Ebola'''
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In a normal immune response interferons (IFN) are produced to alert surrounding cells to the presence of a pathogen, which activates STAT1 by phosphorylation(2). STAT1 is a transcription factor that increases production of immune fighting genes in cells, STAT1 is brought to the nucleus by karyopherin α proteins(2). Ebola protein VP24 <scene name='60/602719/Vp24_bound_to_karyopherin_a5/1'>binds to karyopherin</scene> α1, α5, and α6, which normally bring the P-STAT1 to the nucleus(3). With the karyopherin proteins bound, P-STAT1 does not make it to the nucleus which greatly weakens the immune response in cells (3).
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In a normal immune response interferons (IFN) are produced to alert surrounding cells to the presence of a pathogen, which activates STAT1 by phosphorylation <ref name='4or8'>pmid 24574400</ref>. STAT1 is a transcription factor that increases production of immune fighting genes in cells, STAT1 is brought to the nucleus by karyopherin α proteins <ref name='4or8'/>. Ebola protein VP24 <scene name='60/602719/Vp24_bound_to_karyopherin_a5/1'>binds to karyopherin</scene> α1, α5, and α6, which normally bring the P-STAT1 to the nucleus(3). With the karyopherin proteins bound, P-STAT1 does not make it to the nucleus which greatly weakens the immune response in cells (3).
'''Marburg'''
'''Marburg'''
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<scene name='60/602719/Chain_b/1'>Ebola Domain</scene> (Reston)
<scene name='60/602719/Chain_b/1'>Ebola Domain</scene> (Reston)
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There are a few structural characteristics only found in the Ebola viruses. At the top of the pyramidal domain, there are α helices present which are thought to interact with the α karyopherin(1). An α helix formed by the N-terminus runs from the top of the "pyramid" to another nearby VP24, where it binds to one of the pockets located underneath the "pyramid"(1).
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There are a few structural characteristics only found in the Ebola viruses. At the top of the pyramidal domain, there are α helices present which are thought to interact with the α karyopherin <ref name='24574400 '/>. An α helix formed by the N-terminus runs from the top of the "pyramid" to another nearby VP24, where it binds to one of the pockets located underneath the "pyramid" <ref name='24574400 '/>.
<scene name='60/602719/Marburg_vp24_domain/1'>Marburg Domain</scene>
<scene name='60/602719/Marburg_vp24_domain/1'>Marburg Domain</scene>
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The Marburg domain has a beta shelf present that sticks out from the structure(1). The Marburg VP24 doesn't use an alpha helix to bind to another VP24 like the Ebola VP24(1). Instead, it uses a flexible strand that binds to a groove of a close-by VP24(1).
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The Marburg domain has a beta shelf present that sticks out from the structure <ref name='24574400 '/>. The Marburg VP24 doesn't use an alpha helix to bind to another VP24 like the Ebola VP24 <ref name='24574400 '/>. Instead, it uses a flexible strand that binds to a groove of a close-by VP24 <ref name='24574400 '/>.
</StructureSection>
</StructureSection>
== References ==
== References ==
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1. Zhang, A.P.P., Bornholdt, Z.A., Abelson, D.M., Saphire, E.O. Crystal Structure of Marburg Virus VP24. J. Virol.2014, Feb 26;88(10):5859
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<references/>
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2. Zhang, P.P., Abelson, D.M., Bornholdt, Z.A., Liu, T., Woods, V.L. Jr., Saphire, E. O. The ebolavirus VP24 interferon antagonist: Know your enemy. Virulence. 2012, Aug 15;3(5)440-445
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3. Xu, W., Edwards, M.R., Borek, D.M., Feagins, A.R., Mittal, A., Alinger, J.B., Berry, K.N., Yen, B., Hamilton, J., Brett, T.J., Pappu, R.V., Leung, D.W., Basler, C.F., Amarasinghe, G.K. Ebola Virus VP24 Targets a Unique NLS Binding Site on Karyopherin Alpha 5 to Selectively Compete with Nuclear Import of Phosphorylated STAT1. Cell Host & Microbe. 2014, Aug 13;16 187-200
3. Xu, W., Edwards, M.R., Borek, D.M., Feagins, A.R., Mittal, A., Alinger, J.B., Berry, K.N., Yen, B., Hamilton, J., Brett, T.J., Pappu, R.V., Leung, D.W., Basler, C.F., Amarasinghe, G.K. Ebola Virus VP24 Targets a Unique NLS Binding Site on Karyopherin Alpha 5 to Selectively Compete with Nuclear Import of Phosphorylated STAT1. Cell Host & Microbe. 2014, Aug 13;16 187-200

Revision as of 07:45, 6 November 2014

VP24

VP24 from the Reston Ebola Virus 4d9o

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References

  1. 1.0 1.1 Zhang AP, Bornholdt ZA, Abelson DM, Saphire EO. Crystal Structure of Marburg Virus VP24. J Virol. 2014 May;88(10):5859-63. doi: 10.1128/JVI.03565-13. Epub 2014 Feb 26. PMID:24574400 doi:http://dx.doi.org/10.1128/JVI.03565-13

3. Xu, W., Edwards, M.R., Borek, D.M., Feagins, A.R., Mittal, A., Alinger, J.B., Berry, K.N., Yen, B., Hamilton, J., Brett, T.J., Pappu, R.V., Leung, D.W., Basler, C.F., Amarasinghe, G.K. Ebola Virus VP24 Targets a Unique NLS Binding Site on Karyopherin Alpha 5 to Selectively Compete with Nuclear Import of Phosphorylated STAT1. Cell Host & Microbe. 2014, Aug 13;16 187-200

4. Edwards, R. M., Johnson, B., Mire, C.E., Xu, W., Shabman, R.S., Speller, L.N., Leung, D.W., Geisbert, T.W., Amarasinghe, G.K., Basler, C.F. The Marburg Virus VP24 Protein Interacts with Keap1 to Activate the Cytoprotective Antioxidant Response Pathway. Cell. 2014, Mar 27. 6 1017-1025

5. Bharat, T.A.M., Noda, T., Riches, J.D., Kraehling, V., Kolesnikova, L., Becker, S., Kawaoka, Y., Briggs, J.A.G. Structural dissection of Ebola virus and its assembly determinants using cryo-electron tomography. PNAS. 2012, Feb 6 109(11) 4275-4280.


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