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Tau Avoids the GTP Cap at Growing Microtubule Plus-Ends

Plus-end tracking proteins (+TIPs) associate with the growing end of microtubules and mediate important cellular functions. The majority of +TIPs are directed to the plus-end through a family of end-binding proteins (EBs), which preferentially bind the stabilizing cap of GTP-tubulin present during m...

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Detalles Bibliográficos
Autores principales: Castle, Brian T., McKibben, Kristen M., Rhoades, Elizabeth, Odde, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691178/
https://www.ncbi.nlm.nih.gov/pubmed/33294790
http://dx.doi.org/10.1016/j.isci.2020.101782
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author Castle, Brian T.
McKibben, Kristen M.
Rhoades, Elizabeth
Odde, David J.
author_facet Castle, Brian T.
McKibben, Kristen M.
Rhoades, Elizabeth
Odde, David J.
author_sort Castle, Brian T.
collection PubMed
description Plus-end tracking proteins (+TIPs) associate with the growing end of microtubules and mediate important cellular functions. The majority of +TIPs are directed to the plus-end through a family of end-binding proteins (EBs), which preferentially bind the stabilizing cap of GTP-tubulin present during microtubule growth. One outstanding question is whether there may exist other microtubule-associated proteins (MAPs) that preferentially bind specific nucleotide states of tubulin. Here, we report that the neuronal MAP tau preferentially binds GDP-tubulin (K(D) = 0.26 μM) over GMPCPP-tubulin (K(D) = 1.1 μM) in vitro, as well as GTP-tubulin at the tips of growing microtubules, causing tau binding to lag behind the plus-end both in vitro and in live cells. Thus, tau is a microtubule tip avoiding protein, establishing the framework for a possible new class of tip avoiding MAPs. We speculate that disease-relevant tau mutations may exert their phenotype by their failure to properly recognize GDP-tubulin.
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spelling pubmed-76911782020-12-07 Tau Avoids the GTP Cap at Growing Microtubule Plus-Ends Castle, Brian T. McKibben, Kristen M. Rhoades, Elizabeth Odde, David J. iScience Article Plus-end tracking proteins (+TIPs) associate with the growing end of microtubules and mediate important cellular functions. The majority of +TIPs are directed to the plus-end through a family of end-binding proteins (EBs), which preferentially bind the stabilizing cap of GTP-tubulin present during microtubule growth. One outstanding question is whether there may exist other microtubule-associated proteins (MAPs) that preferentially bind specific nucleotide states of tubulin. Here, we report that the neuronal MAP tau preferentially binds GDP-tubulin (K(D) = 0.26 μM) over GMPCPP-tubulin (K(D) = 1.1 μM) in vitro, as well as GTP-tubulin at the tips of growing microtubules, causing tau binding to lag behind the plus-end both in vitro and in live cells. Thus, tau is a microtubule tip avoiding protein, establishing the framework for a possible new class of tip avoiding MAPs. We speculate that disease-relevant tau mutations may exert their phenotype by their failure to properly recognize GDP-tubulin. Elsevier 2020-11-06 /pmc/articles/PMC7691178/ /pubmed/33294790 http://dx.doi.org/10.1016/j.isci.2020.101782 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Castle, Brian T.
McKibben, Kristen M.
Rhoades, Elizabeth
Odde, David J.
Tau Avoids the GTP Cap at Growing Microtubule Plus-Ends
title Tau Avoids the GTP Cap at Growing Microtubule Plus-Ends
title_full Tau Avoids the GTP Cap at Growing Microtubule Plus-Ends
title_fullStr Tau Avoids the GTP Cap at Growing Microtubule Plus-Ends
title_full_unstemmed Tau Avoids the GTP Cap at Growing Microtubule Plus-Ends
title_short Tau Avoids the GTP Cap at Growing Microtubule Plus-Ends
title_sort tau avoids the gtp cap at growing microtubule plus-ends
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691178/
https://www.ncbi.nlm.nih.gov/pubmed/33294790
http://dx.doi.org/10.1016/j.isci.2020.101782
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