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Modeling of the SV40 DNA Replication Machine

The mechanism of SV40 DNA replication is certainly not completely understood. The proteins that are necessary for replication have been known for quite some time, but how they work together to form a nanomachine capable of faithfully replicating the virus DNA is only partially understood. Some of th...

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Autor principal: Simmons, Daniel T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902795/
https://www.ncbi.nlm.nih.gov/pubmed/24705083
http://dx.doi.org/10.3390/genes3040742
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author Simmons, Daniel T
author_facet Simmons, Daniel T
author_sort Simmons, Daniel T
collection PubMed
description The mechanism of SV40 DNA replication is certainly not completely understood. The proteins that are necessary for replication have been known for quite some time, but how they work together to form a nanomachine capable of faithfully replicating the virus DNA is only partially understood. Some of the proteins involved have been crystallized and their 3D structures determined, and several EM reconstructions of SV40 T antigen have been generated. In addition, there is a fair amount of biochemical data that pinpoints the sites of interaction between various proteins. With this information, various models were assembled that show how the SV40 DNA replication nanomachine could be structured in three dimensional space. This process was aided by the use of a 3D docking program as well as fitting of structures. The advantage of the availability of these models is that they are experimentally testable and they provide an insight into how the replication machine could work. Another advantage is that it is possible to quickly compare newly published structures to the models in order to come up with improved models.
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spelling pubmed-39027952014-03-26 Modeling of the SV40 DNA Replication Machine Simmons, Daniel T Genes (Basel) Concept Paper The mechanism of SV40 DNA replication is certainly not completely understood. The proteins that are necessary for replication have been known for quite some time, but how they work together to form a nanomachine capable of faithfully replicating the virus DNA is only partially understood. Some of the proteins involved have been crystallized and their 3D structures determined, and several EM reconstructions of SV40 T antigen have been generated. In addition, there is a fair amount of biochemical data that pinpoints the sites of interaction between various proteins. With this information, various models were assembled that show how the SV40 DNA replication nanomachine could be structured in three dimensional space. This process was aided by the use of a 3D docking program as well as fitting of structures. The advantage of the availability of these models is that they are experimentally testable and they provide an insight into how the replication machine could work. Another advantage is that it is possible to quickly compare newly published structures to the models in order to come up with improved models. MDPI 2012-11-09 /pmc/articles/PMC3902795/ /pubmed/24705083 http://dx.doi.org/10.3390/genes3040742 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Concept Paper
Simmons, Daniel T
Modeling of the SV40 DNA Replication Machine
title Modeling of the SV40 DNA Replication Machine
title_full Modeling of the SV40 DNA Replication Machine
title_fullStr Modeling of the SV40 DNA Replication Machine
title_full_unstemmed Modeling of the SV40 DNA Replication Machine
title_short Modeling of the SV40 DNA Replication Machine
title_sort modeling of the sv40 dna replication machine
topic Concept Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902795/
https://www.ncbi.nlm.nih.gov/pubmed/24705083
http://dx.doi.org/10.3390/genes3040742
work_keys_str_mv AT simmonsdanielt modelingofthesv40dnareplicationmachine