Repositorio Institucional de la Universidad Alfonso X el Sabio

A Novel Systems-Biology Algorithm for the Analysis of Coordinated Protein Responses Using Quantitative Proteomics

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APA

García Marqués, Fernando & Trevisan Herraz, Marco & Martínez Martínez, Sara & Camafeita, Emilio & Jorge, Inmaculada & López, Juan Antonio & Méndez Barbero, Nerea & Méndez Ferrer, Simón & del Pozo, Miguel Angel & Ibáñez, Borja & Andrés, Vicente & Sánchez Madrid, Francisco & Redondo, Juan Miguel & Bonzon Kulichenko, Elena & Vázquez, Jesús (2016-05 ) .A Novel Systems-Biology Algorithm for the Analysis of Coordinated Protein Responses Using Quantitative Proteomics.

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García Marqués, Fernando & Trevisan Herraz, Marco & Martínez Martínez, Sara & Camafeita, Emilio & Jorge, Inmaculada & López, Juan Antonio & Méndez Barbero, Nerea & Méndez Ferrer, Simón & del Pozo, Miguel Angel & Ibáñez, Borja & Andrés, Vicente & Sánchez Madrid, Francisco & Redondo, Juan Miguel & Bonzon Kulichenko, Elena & Vázquez, Jesús. 2016-05 .A Novel Systems-Biology Algorithm for the Analysis of Coordinated Protein Responses Using Quantitative Proteomics.

https://hdl.handle.net/20.500.12080/45598
dc.contributor.author García Marqués, Fernando
dc.contributor.author Trevisan Herraz, Marco
dc.contributor.author Martínez Martínez, Sara
dc.contributor.author Camafeita, Emilio
dc.contributor.author Jorge, Inmaculada
dc.contributor.author López, Juan Antonio
dc.contributor.author Méndez Barbero, Nerea
dc.contributor.author Méndez Ferrer, Simón
dc.contributor.author del Pozo, Miguel Angel
dc.contributor.author Ibáñez, Borja
dc.contributor.author Andrés, Vicente
dc.contributor.author Sánchez Madrid, Francisco
dc.contributor.author Redondo, Juan Miguel
dc.contributor.author Bonzon Kulichenko, Elena
dc.contributor.author Vázquez, Jesús
dc.date.accessioned 2025-03-12T16:10:58Z
dc.date.available 2025-03-12T16:10:58Z
dc.date.created 2016-05
dc.date.issued 2016-05
dc.identifier.uri https://hdl.handle.net/20.500.12080/45598
dc.description.abstract The coordinated behavior of proteins is central to systems biology. However, the underlying mechanisms are poorly known and methods to analyze coordination by conventional quantitative proteomics are still lacking. We present the Systems Biology Triangle (SBT), a new algorithm that allows the study of protein coordination by pairwise quantitative proteomics. The Systems Biology Triangle detected statistically significant coordination in diverse biological models of very different nature and subjected to different kinds of perturbations. The Systems Biology Triangle also revealed with unprecedented molecular detail an array of coordinated, early protein responses in vascular smooth muscle cells treated at different times with angiotensin-II. These responses included activation of protein synthesis, folding, turnover, and muscle contraction ¿ consistent with a differentiated phenotype¿as well as the induction of migration and the repression of cell proliferation and secretion. Remarkably, the majority of the altered functional categories were protein complexes, interaction networks, or metabolic pathways. These changes could not be detected by other algorithms widely used by the proteomics community, and the vast majority of proteins involved have not been described before to be regulated by AngII. The unique capabilities of The Systems Biology Triangle to detect functional protein alterations produced by the coordinated action of proteins in pairwise quantitative proteomics experiments make this algorithm an attractive choice for the biological interpretation of results on a routine basis. es_ES
dc.format application/pdf es_ES
dc.language eng es_ES
dc.relation.ispartof Molecular & Cellular Proteomics es_ES
dc.rights CC-BY es_ES
dc.rights.uri http://creativecommons.org/licenses/by/4.0/deed.es es_ES
dc.source Molecular & Cellular Proteomics es_ES
dc.title A Novel Systems-Biology Algorithm for the Analysis of Coordinated Protein Responses Using Quantitative Proteomics es_ES
dc.type info:eu-repo/semantics/article es_ES
dc.rights.accessrights info:eu-repo/semantics/openAccess es_ES
dc.identifier.location N/A es_ES


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