Literature DB >> 21524670

The Haemonchus contortus UNC-49B subunit possesses the residues required for GABA sensitivity in homomeric and heteromeric channels.

Michael V Accardi1, Sean G Forrester.   

Abstract

Hco-UNC-49 is a GABA receptor from the parasitic nematode Haemonchus contortus that has a relatively low overall sequence similarity to vertebrate GABA receptors but is very similar to the UNC-49 receptor found in the free living nematode Caenorhabditis elegans. While the nematode receptors do share >80% sequence similarity they exhibit different sensitivities to GABA. In addition, the UNC-49C subunit appears to be a positive modulator of GABA sensitivity in the H. contortus heteromeric channel, but is a negative modulator in the C. elegans heteromeric channel. The cause(s) of these differences is currently unknown since the structural elements essential for GABA sensitivity in nematode receptors have been largely unexplored. Thus, the overall aim of this study was to investigate the residues that are important for UNC-49 receptor sensitivity through the use of homology modeling, site-directed mutagenesis, and two-electrode voltage clamp. This study revealed that Met(170) in Loop B of the GABA binding-site may partially account for the observed differences in GABA receptor sensitivity between the nematode species. Residues in Loops A-D that have been reported to form the GABA binding pocket in mammalian receptors, including those forming the conserved 'aromatic box', also appear to play analogous roles in Hco-UNC-49. In addition, the two mutations that produced the most significant reduction in GABA sensitivity were R66S and Y166S. Homology modeling indicates that these two residues share a hydrogen bond and are positioned close to the carboxyl end of the GABA molecule. However, of residues examined in this study, only those on the Hco-UNC-49B subunit and not its subunit partner, Hco-UNC-49C, appear important for GABA sensitivity. Overall, results from this study suggest that the binding site of the UNC-49 heteromeric GABA receptor exhibits some differences compared to classical vertebrate GABA(A) receptors.
Copyright © 2011 Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21524670     DOI: 10.1016/j.molbiopara.2011.04.002

Source DB:  PubMed          Journal:  Mol Biochem Parasitol        ISSN: 0166-6851            Impact factor:   1.759


  5 in total

Review 1.  Nematode cys-loop GABA receptors: biological function, pharmacology and sites of action for anthelmintics.

Authors:  Michael V Accardi; Robin N Beech; Sean G Forrester
Journal:  Invert Neurosci       Date:  2012-03-20

2.  A molecular characterization of the agonist binding site of a nematode cys-loop GABA receptor.

Authors:  Mark D Kaji; Ariel Kwaka; Micah K Callanan; Humza Nusrat; Jean-Paul Desaulniers; Sean G Forrester
Journal:  Br J Pharmacol       Date:  2015-05-19       Impact factor: 8.739

3.  Molecular basis for convergent evolution of glutamate recognition by pentameric ligand-gated ion channels.

Authors:  Timothy Lynagh; Robin N Beech; Maryline J Lalande; Kevin Keller; Brett A Cromer; Adrian J Wolstenholme; Bodo Laube
Journal:  Sci Rep       Date:  2015-02-24       Impact factor: 4.379

4.  Recent Duplication and Functional Divergence in Parasitic Nematode Levamisole-Sensitive Acetylcholine Receptors.

Authors:  Thomas B Duguet; Claude L Charvet; Sean G Forrester; Claudia M Wever; Joseph A Dent; Cedric Neveu; Robin N Beech
Journal:  PLoS Negl Trop Dis       Date:  2016-07-14

5.  A mutational and molecular dynamics study of the cys-loop GABA receptor Hco-UNC-49 from Haemonchus contortus: Agonist recognition in the nematode GABA receptor family.

Authors:  Josh Foster; Everett Cochrane; Mohammad Hassan Khatami; Sarah A Habibi; Hendrick de Haan; Sean G Forrester
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2018-10-06       Impact factor: 4.077

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.