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Kinetic and cell-based analyses of GTPase regulators

Regulatory GTPases are often portrayed as binary molecular switches that control a wide range of cellular processes, including, but not limited to, the generation of second messengers (e.g., cAMP and inositol phosphates), intracellular traffic, cytoskeleton organization and cell proliferation. GEF s...

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Detalles Bibliográficos
Autores principales: Segev, Nava, Kahn, Richard A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3498071/
https://www.ncbi.nlm.nih.gov/pubmed/23181195
http://dx.doi.org/10.4161/cl.22645
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author Segev, Nava
Kahn, Richard A.
author_facet Segev, Nava
Kahn, Richard A.
author_sort Segev, Nava
collection PubMed
description Regulatory GTPases are often portrayed as binary molecular switches that control a wide range of cellular processes, including, but not limited to, the generation of second messengers (e.g., cAMP and inositol phosphates), intracellular traffic, cytoskeleton organization and cell proliferation. GEF stimulators and GAP inhibitors regulate the nucleotide-bound state of these proteins. Because of the relevance of GTPases and their regulators to human diseases, they comprise a major therapeutic target. Currently, most of the information about GTPase regulators comes from structure analyses. Such structural information is limited to certain conditions and does not necessarily reflect specificity or physiological activity. To address questions about specificity and mechanisms of action, kinetic and cell-based analyses of GTPase regulators is necessary. Here, we compare these two approaches in the context of regulators of Arf and heterotrimeric G-proteins.
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spelling pubmed-34980712012-11-23 Kinetic and cell-based analyses of GTPase regulators Segev, Nava Kahn, Richard A. Cell Logist Editorial Regulatory GTPases are often portrayed as binary molecular switches that control a wide range of cellular processes, including, but not limited to, the generation of second messengers (e.g., cAMP and inositol phosphates), intracellular traffic, cytoskeleton organization and cell proliferation. GEF stimulators and GAP inhibitors regulate the nucleotide-bound state of these proteins. Because of the relevance of GTPases and their regulators to human diseases, they comprise a major therapeutic target. Currently, most of the information about GTPase regulators comes from structure analyses. Such structural information is limited to certain conditions and does not necessarily reflect specificity or physiological activity. To address questions about specificity and mechanisms of action, kinetic and cell-based analyses of GTPase regulators is necessary. Here, we compare these two approaches in the context of regulators of Arf and heterotrimeric G-proteins. Landes Bioscience 2012-07-01 /pmc/articles/PMC3498071/ /pubmed/23181195 http://dx.doi.org/10.4161/cl.22645 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Editorial
Segev, Nava
Kahn, Richard A.
Kinetic and cell-based analyses of GTPase regulators
title Kinetic and cell-based analyses of GTPase regulators
title_full Kinetic and cell-based analyses of GTPase regulators
title_fullStr Kinetic and cell-based analyses of GTPase regulators
title_full_unstemmed Kinetic and cell-based analyses of GTPase regulators
title_short Kinetic and cell-based analyses of GTPase regulators
title_sort kinetic and cell-based analyses of gtpase regulators
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3498071/
https://www.ncbi.nlm.nih.gov/pubmed/23181195
http://dx.doi.org/10.4161/cl.22645
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