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Stability and membrane interactions of an autotransport protein: MD simulations of the Hia translocator domain in a complex membrane environment

Stability and membrane interactions of an autotransport protein: MD simulations of the Hia translocator domain in a complex membrane environment
Stability and membrane interactions of an autotransport protein: MD simulations of the Hia translocator domain in a complex membrane environment
Hia is a trimeric autotransporter found in the outer membrane of Haemphilus influenzae. The X-ray structure of Hia translocator domain revealed each monomer to consist of an ?-helix connected via a loop to a 4-stranded ?-sheet, thus the topology of the trimeric translocator domain is a 12-stranded ?-barrel containing 3 ?-helices that protrude from the mouth of the ?-barrel into the extracellular medium. Molecular dynamics simulations of the Hia monomer and trimer have been employed to explore the interactions between the helices, ?-barrel and connecting loops that may contribute to the stability of the trimer. In simulations of the Hia monomer we show that the central ?-helix may stabilise the fold of the 4-stranded ?-sheet. In simulations of the Hia trimer, a H-bond network involving residues in the ?-barrel, ?-helices and loops has been identified as providing stability for the trimeric arrangement of the monomers. Glutamine residues located in the loops connecting the ?-helices to the ?-barrel are orientated in a triangular arrangement such that each forms 2 hydrogen bonds to each of the corresponding glutamines in the other loops. In the absence of the loops, the ??barrel becomes distorted. Simulations show that while the trimeric translocator domain ?-barrel is inherently flexible, it is unlikely to accommodate the passenger domain in a folded conformation. Simulations of Hia in an asymmetric model of the outer membrane have revealed membrane–protein interactions that anchor the protein within its native membrane environment.
autotransporter, membrane protein, molecular dynamics
0304-4165
715-723
Holdbrook, Daniel A.
d114c018-fb42-4a49-9b50-f7739feb75f5
Piggot, Thomas J.
75829b71-d73b-43d1-b24f-3e70c2c4d0c8
Sansom, Mark S.P.
ed30b4fc-bc73-4ad7-8c56-f51a67136e4e
Khalid, Syma
90fbd954-7248-4f47-9525-4d6af9636394
Holdbrook, Daniel A.
d114c018-fb42-4a49-9b50-f7739feb75f5
Piggot, Thomas J.
75829b71-d73b-43d1-b24f-3e70c2c4d0c8
Sansom, Mark S.P.
ed30b4fc-bc73-4ad7-8c56-f51a67136e4e
Khalid, Syma
90fbd954-7248-4f47-9525-4d6af9636394

Holdbrook, Daniel A., Piggot, Thomas J., Sansom, Mark S.P. and Khalid, Syma (2013) Stability and membrane interactions of an autotransport protein: MD simulations of the Hia translocator domain in a complex membrane environment. Biochimica et Biophysica Acta (BBA) - Biomembranes, 1828 (2), 715-723. (doi:10.1016/j.bbamem.2012.09.002). (PMID:22982599)

Record type: Article

Abstract

Hia is a trimeric autotransporter found in the outer membrane of Haemphilus influenzae. The X-ray structure of Hia translocator domain revealed each monomer to consist of an ?-helix connected via a loop to a 4-stranded ?-sheet, thus the topology of the trimeric translocator domain is a 12-stranded ?-barrel containing 3 ?-helices that protrude from the mouth of the ?-barrel into the extracellular medium. Molecular dynamics simulations of the Hia monomer and trimer have been employed to explore the interactions between the helices, ?-barrel and connecting loops that may contribute to the stability of the trimer. In simulations of the Hia monomer we show that the central ?-helix may stabilise the fold of the 4-stranded ?-sheet. In simulations of the Hia trimer, a H-bond network involving residues in the ?-barrel, ?-helices and loops has been identified as providing stability for the trimeric arrangement of the monomers. Glutamine residues located in the loops connecting the ?-helices to the ?-barrel are orientated in a triangular arrangement such that each forms 2 hydrogen bonds to each of the corresponding glutamines in the other loops. In the absence of the loops, the ??barrel becomes distorted. Simulations show that while the trimeric translocator domain ?-barrel is inherently flexible, it is unlikely to accommodate the passenger domain in a folded conformation. Simulations of Hia in an asymmetric model of the outer membrane have revealed membrane–protein interactions that anchor the protein within its native membrane environment.

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More information

e-pub ahead of print date: 13 September 2012
Published date: February 2013
Keywords: autotransporter, membrane protein, molecular dynamics
Organisations: Computational Systems Chemistry

Identifiers

Local EPrints ID: 356320
URI: http://eprints.soton.ac.uk/id/eprint/356320
ISSN: 0304-4165
PURE UUID: f3068bbd-aa08-459f-8a6f-213bc45f9d71
ORCID for Syma Khalid: ORCID iD orcid.org/0000-0002-3694-5044

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Date deposited: 18 Sep 2013 16:17
Last modified: 15 Mar 2024 03:29

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Contributors

Author: Daniel A. Holdbrook
Author: Thomas J. Piggot
Author: Mark S.P. Sansom
Author: Syma Khalid ORCID iD

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