Sandbox Reserved 1487
From Proteopedia
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{{Sandbox_Reserved_ESBS}}<!-- PLEASE ADD YOUR CONTENT BELOW HERE --> | {{Sandbox_Reserved_ESBS}}<!-- PLEASE ADD YOUR CONTENT BELOW HERE --> | ||
==Your Heading Here (maybe something like 'Structure')== | ==Your Heading Here (maybe something like 'Structure')== | ||
- | <StructureSection load='1ki4' size='340' side='right' caption=' | + | <StructureSection load='1ki4' size='340' side='right' caption='Thymidine kinase from Herpes simplex virus type I compexes with 5-bromothienyldeoxyuridine' scene=''> |
This is a default text for your page ''''''. Click above on '''edit this page''' to modify. Be careful with the < and > signs. | This is a default text for your page ''''''. Click above on '''edit this page''' to modify. Be careful with the < and > signs. | ||
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue. | You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue. | ||
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The role of kinase is to catalyse protein phosphorylation. To do this, they transmit a phosphate group to the protein in the side chain of an amino acid chains. The phosphate group comes from the hydrolysis of ATP in ADP. This reaction can be in both directions. | The role of kinase is to catalyse protein phosphorylation. To do this, they transmit a phosphate group to the protein in the side chain of an amino acid chains. The phosphate group comes from the hydrolysis of ATP in ADP. This reaction can be in both directions. | ||
- | The HSV1-TK is involved in the reactivation of Herpes simplex virus. Indeed this protein is involved in the salvage pathway of pyrimidine synthesis. As seen previously, this enzyme allows to transfert the γ phosphate group from ATP to the deoxythymidine | + | The HSV1-TK is involved in the reactivation of Herpes simplex virus. Indeed this protein is involved in the salvage pathway of pyrimidine synthesis. As seen previously, this enzyme allows to transfert the γ phosphate group from ATP to the deoxythymidine to generate deoxythymidine monophosphate.[[Image:reaction.jpeg]] |
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After the first infection, wounds can reappear, and the frequency depends on person. Antivirals are used to reduce the viral load of people infected but they do not cure the infection. However, a mutation in the HSV1-TK protein causes the resistance of the virus against antivirals in immunocompromised patients. | After the first infection, wounds can reappear, and the frequency depends on person. Antivirals are used to reduce the viral load of people infected but they do not cure the infection. However, a mutation in the HSV1-TK protein causes the resistance of the virus against antivirals in immunocompromised patients. | ||
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+ | == Therapeutic application == | ||
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+ | The first suicide gene system developed for a therapeutic gene use, uses the thymidine kinase from Herpes simplex type I virus. | ||
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+ | The aim was to develop a gene encoding an enzyme that performs an activity normally absent in the target cells of the therapy. This enzyme would then allow the synthesis of toxic compounds. | ||
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+ | Aciclovir (ACV) and Ganciclovir (GVC) are 2 nucleosides analogues of guanosine. These are metabolized by HSV1-TK to a monophosphoryl compound which is then transformed into di and tri phosphate metabolites by cellular kinases. Then, ACV-TP and GVC-TP are incorporated into DNA during the elongation causing the death of infected cells by apoptosis. They also inhibit the viral replication. Death of cells is also triggered when they are treated with GVC when there has been an upstream transfection of the HSV1-TK gene outside a viral infection. | ||
Revision as of 17:36, 10 January 2019
This Sandbox is Reserved from 06/12/2018, through 30/06/2019 for use in the course "Structural Biology" taught by Bruno Kieffer at the University of Strasbourg, ESBS. This reservation includes Sandbox Reserved 1480 through Sandbox Reserved 1543. |
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References
- ↑ Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
- ↑ Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644