A virtual high-throughput screening approach to the discovery of novel inhibitors of the bacterial leucine transporter, LeuT

Katie J Simmons; Kamil Gotfryd; Christian B Billesbølle; Claus J Loland; Ulrik Gether; Colin W G Fishwick; A Peter Johnson

doi:10.3109/09687688.2012.710341

A virtual high-throughput screening approach to the discovery of novel inhibitors of the bacterial leucine transporter, LeuT

Katie J Simmons, Kamil Gotfryd, Christian B Billesbølle, Claus J Loland, Ulrik Gether, Colin W G Fishwick, A Peter Johnson

Neuropharm and Genetics

Abstract

Membrane proteins are intrinsically involved in both human and pathogen physiology, and are the target of 60% of all marketed drugs. During the past decade, advances in the studies of membrane proteins using X-ray crystallography, electron microscopy and NMR-based techniques led to the elucidation of over 250 unique membrane protein crystal structures. The aim of the European Drug Initiative for Channels and Transporter (EDICT) project is to use the structures of clinically significant membrane proteins for the development of lead molecules. One of the approaches used to achieve this is a virtual high-throughput screening (vHTS) technique initially developed for soluble proteins. This paper describes application of this technique to the discovery of inhibitors of the leucine transporter (LeuT), a member of the neurotransmitter:sodium symporter (NSS) family.

Originalsprog	Engelsk
Tidsskrift	Molecular Membrane Biology
Vol/bind	30
Udgave nummer	2
Sider (fra-til)	184-94
Antal sider	11
ISSN	0968-7688
DOI	https://doi.org/10.3109/09687688.2012.710341
Status	Udgivet - mar. 2013

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10.3109/09687688.2012.710341

Citationsformater

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title = "A virtual high-throughput screening approach to the discovery of novel inhibitors of the bacterial leucine transporter, LeuT",

abstract = "Membrane proteins are intrinsically involved in both human and pathogen physiology, and are the target of 60% of all marketed drugs. During the past decade, advances in the studies of membrane proteins using X-ray crystallography, electron microscopy and NMR-based techniques led to the elucidation of over 250 unique membrane protein crystal structures. The aim of the European Drug Initiative for Channels and Transporter (EDICT) project is to use the structures of clinically significant membrane proteins for the development of lead molecules. One of the approaches used to achieve this is a virtual high-throughput screening (vHTS) technique initially developed for soluble proteins. This paper describes application of this technique to the discovery of inhibitors of the leucine transporter (LeuT), a member of the neurotransmitter:sodium symporter (NSS) family.",

author = "Simmons, {Katie J} and Kamil Gotfryd and Billesb{\o}lle, {Christian B} and Loland, {Claus J} and Ulrik Gether and Fishwick, {Colin W G} and Johnson, {A Peter}",

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AU - Simmons, Katie J

AU - Gotfryd, Kamil

AU - Billesbølle, Christian B

AU - Loland, Claus J

AU - Gether, Ulrik

AU - Fishwick, Colin W G

AU - Johnson, A Peter

PY - 2013/3

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N2 - Membrane proteins are intrinsically involved in both human and pathogen physiology, and are the target of 60% of all marketed drugs. During the past decade, advances in the studies of membrane proteins using X-ray crystallography, electron microscopy and NMR-based techniques led to the elucidation of over 250 unique membrane protein crystal structures. The aim of the European Drug Initiative for Channels and Transporter (EDICT) project is to use the structures of clinically significant membrane proteins for the development of lead molecules. One of the approaches used to achieve this is a virtual high-throughput screening (vHTS) technique initially developed for soluble proteins. This paper describes application of this technique to the discovery of inhibitors of the leucine transporter (LeuT), a member of the neurotransmitter:sodium symporter (NSS) family.

AB - Membrane proteins are intrinsically involved in both human and pathogen physiology, and are the target of 60% of all marketed drugs. During the past decade, advances in the studies of membrane proteins using X-ray crystallography, electron microscopy and NMR-based techniques led to the elucidation of over 250 unique membrane protein crystal structures. The aim of the European Drug Initiative for Channels and Transporter (EDICT) project is to use the structures of clinically significant membrane proteins for the development of lead molecules. One of the approaches used to achieve this is a virtual high-throughput screening (vHTS) technique initially developed for soluble proteins. This paper describes application of this technique to the discovery of inhibitors of the leucine transporter (LeuT), a member of the neurotransmitter:sodium symporter (NSS) family.

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DO - 10.3109/09687688.2012.710341

M3 - Journal article

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SN - 0968-7688

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EP - 194

JO - Membrane Biochemistry

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ER -

A virtual high-throughput screening approach to the discovery of novel inhibitors of the bacterial leucine transporter, LeuT

Abstract

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