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A Novel Family of Apicomplexan Glideosome-associated Proteins with an Inner Membrane-anchoring Role

The phylum Apicomplexa are a group of obligate intracellular parasites responsible for a wide range of important diseases. Central to the lifecycle of these unicellular parasites is their ability to migrate through animal tissue and invade target host cells. Apicomplexan movement is generated by a u...

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Autores principales: Bullen, Hayley E., Tonkin, Christopher J., O'Donnell, Rebecca A., Tham, Wai-Hong, Papenfuss, Anthony T., Gould, Sven, Cowman, Alan F., Crabb, Brendan S., Gilson, Paul R.
Formato: Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2757237/
https://www.ncbi.nlm.nih.gov/pubmed/19561073
http://dx.doi.org/10.1074/jbc.M109.036772
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author Bullen, Hayley E.
Tonkin, Christopher J.
O'Donnell, Rebecca A.
Tham, Wai-Hong
Papenfuss, Anthony T.
Gould, Sven
Cowman, Alan F.
Crabb, Brendan S.
Gilson, Paul R.
author_facet Bullen, Hayley E.
Tonkin, Christopher J.
O'Donnell, Rebecca A.
Tham, Wai-Hong
Papenfuss, Anthony T.
Gould, Sven
Cowman, Alan F.
Crabb, Brendan S.
Gilson, Paul R.
author_sort Bullen, Hayley E.
collection PubMed
description The phylum Apicomplexa are a group of obligate intracellular parasites responsible for a wide range of important diseases. Central to the lifecycle of these unicellular parasites is their ability to migrate through animal tissue and invade target host cells. Apicomplexan movement is generated by a unique system of gliding motility in which substrate adhesins and invasion-related proteins are pulled across the plasma membrane by an underlying actin-myosin motor. The myosins of this motor are inserted into a dual membrane layer called the inner membrane complex (IMC) that is sandwiched between the plasma membrane and an underlying cytoskeletal basket. Central to our understanding of gliding motility is the characterization of proteins residing within the IMC, but to date only a few proteins are known. We report here a novel family of six-pass transmembrane proteins, termed the GAPM family, which are highly conserved and specific to Apicomplexa. In Plasmodium falciparum and Toxoplasma gondii the GAPMs localize to the IMC where they form highly SDS-resistant oligomeric complexes. The GAPMs co-purify with the cytoskeletal alveolin proteins and also to some degree with the actin-myosin motor itself. Hence, these proteins are strong candidates for an IMC-anchoring role, either directly or indirectly tethering the motor to the cytoskeleton.
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spelling pubmed-27572372009-10-13 A Novel Family of Apicomplexan Glideosome-associated Proteins with an Inner Membrane-anchoring Role Bullen, Hayley E. Tonkin, Christopher J. O'Donnell, Rebecca A. Tham, Wai-Hong Papenfuss, Anthony T. Gould, Sven Cowman, Alan F. Crabb, Brendan S. Gilson, Paul R. J Biol Chem Protein Structure and Folding The phylum Apicomplexa are a group of obligate intracellular parasites responsible for a wide range of important diseases. Central to the lifecycle of these unicellular parasites is their ability to migrate through animal tissue and invade target host cells. Apicomplexan movement is generated by a unique system of gliding motility in which substrate adhesins and invasion-related proteins are pulled across the plasma membrane by an underlying actin-myosin motor. The myosins of this motor are inserted into a dual membrane layer called the inner membrane complex (IMC) that is sandwiched between the plasma membrane and an underlying cytoskeletal basket. Central to our understanding of gliding motility is the characterization of proteins residing within the IMC, but to date only a few proteins are known. We report here a novel family of six-pass transmembrane proteins, termed the GAPM family, which are highly conserved and specific to Apicomplexa. In Plasmodium falciparum and Toxoplasma gondii the GAPMs localize to the IMC where they form highly SDS-resistant oligomeric complexes. The GAPMs co-purify with the cytoskeletal alveolin proteins and also to some degree with the actin-myosin motor itself. Hence, these proteins are strong candidates for an IMC-anchoring role, either directly or indirectly tethering the motor to the cytoskeleton. American Society for Biochemistry and Molecular Biology 2009-09-11 2009-06-26 /pmc/articles/PMC2757237/ /pubmed/19561073 http://dx.doi.org/10.1074/jbc.M109.036772 Text en © 2009 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) applies to Author Choice Articles
spellingShingle Protein Structure and Folding
Bullen, Hayley E.
Tonkin, Christopher J.
O'Donnell, Rebecca A.
Tham, Wai-Hong
Papenfuss, Anthony T.
Gould, Sven
Cowman, Alan F.
Crabb, Brendan S.
Gilson, Paul R.
A Novel Family of Apicomplexan Glideosome-associated Proteins with an Inner Membrane-anchoring Role
title A Novel Family of Apicomplexan Glideosome-associated Proteins with an Inner Membrane-anchoring Role
title_full A Novel Family of Apicomplexan Glideosome-associated Proteins with an Inner Membrane-anchoring Role
title_fullStr A Novel Family of Apicomplexan Glideosome-associated Proteins with an Inner Membrane-anchoring Role
title_full_unstemmed A Novel Family of Apicomplexan Glideosome-associated Proteins with an Inner Membrane-anchoring Role
title_short A Novel Family of Apicomplexan Glideosome-associated Proteins with an Inner Membrane-anchoring Role
title_sort novel family of apicomplexan glideosome-associated proteins with an inner membrane-anchoring role
topic Protein Structure and Folding
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2757237/
https://www.ncbi.nlm.nih.gov/pubmed/19561073
http://dx.doi.org/10.1074/jbc.M109.036772
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