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A Screen for Membrane Fission Catalysts Identifies the ATPase EHD1

[Image: see text] Membrane fission manifests during cell division, synaptic transmission, vesicular transport, and organelle biogenesis, yet identifying proteins that catalyze fission remains a challenge. Using a facile and robust assay system of supported membrane tubes in a microscopic screen that...

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Autores principales: Kamerkar, Sukrut C., Roy, Krishnendu, Bhattacharyya, Soumya, Pucadyil, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327249/
https://www.ncbi.nlm.nih.gov/pubmed/30403133
http://dx.doi.org/10.1021/acs.biochem.8b00925
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author Kamerkar, Sukrut C.
Roy, Krishnendu
Bhattacharyya, Soumya
Pucadyil, Thomas J.
author_facet Kamerkar, Sukrut C.
Roy, Krishnendu
Bhattacharyya, Soumya
Pucadyil, Thomas J.
author_sort Kamerkar, Sukrut C.
collection PubMed
description [Image: see text] Membrane fission manifests during cell division, synaptic transmission, vesicular transport, and organelle biogenesis, yet identifying proteins that catalyze fission remains a challenge. Using a facile and robust assay system of supported membrane tubes in a microscopic screen that directly monitors membrane tube scission, we detect robust GTP- and ATP-dependent as well as nucleotide-independent fission activity in the brain cytosol. Using previously established interacting partner proteins as bait for pulldowns, we attribute the GTP-dependent fission activity to dynamin. Biochemical fractionation followed by mass spectrometric analyses identifies the Eps15-homology domain-containing protein1 (EHD1) as a novel ATP-dependent membrane fission catalyst. Together, our approach establishes an experimental workflow for the discovery of novel membrane fission catalysts.
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spelling pubmed-63272492019-01-17 A Screen for Membrane Fission Catalysts Identifies the ATPase EHD1 Kamerkar, Sukrut C. Roy, Krishnendu Bhattacharyya, Soumya Pucadyil, Thomas J. Biochemistry [Image: see text] Membrane fission manifests during cell division, synaptic transmission, vesicular transport, and organelle biogenesis, yet identifying proteins that catalyze fission remains a challenge. Using a facile and robust assay system of supported membrane tubes in a microscopic screen that directly monitors membrane tube scission, we detect robust GTP- and ATP-dependent as well as nucleotide-independent fission activity in the brain cytosol. Using previously established interacting partner proteins as bait for pulldowns, we attribute the GTP-dependent fission activity to dynamin. Biochemical fractionation followed by mass spectrometric analyses identifies the Eps15-homology domain-containing protein1 (EHD1) as a novel ATP-dependent membrane fission catalyst. Together, our approach establishes an experimental workflow for the discovery of novel membrane fission catalysts. American Chemical Society 2018-11-07 2019-01-08 /pmc/articles/PMC6327249/ /pubmed/30403133 http://dx.doi.org/10.1021/acs.biochem.8b00925 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Kamerkar, Sukrut C.
Roy, Krishnendu
Bhattacharyya, Soumya
Pucadyil, Thomas J.
A Screen for Membrane Fission Catalysts Identifies the ATPase EHD1
title A Screen for Membrane Fission Catalysts Identifies the ATPase EHD1
title_full A Screen for Membrane Fission Catalysts Identifies the ATPase EHD1
title_fullStr A Screen for Membrane Fission Catalysts Identifies the ATPase EHD1
title_full_unstemmed A Screen for Membrane Fission Catalysts Identifies the ATPase EHD1
title_short A Screen for Membrane Fission Catalysts Identifies the ATPase EHD1
title_sort screen for membrane fission catalysts identifies the atpase ehd1
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327249/
https://www.ncbi.nlm.nih.gov/pubmed/30403133
http://dx.doi.org/10.1021/acs.biochem.8b00925
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