The A- and B-type muscarinic acetylcholine receptors from Drosophila melanogaster couple to different second messenger pathways

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The A- and B-type muscarinic acetylcholine receptors from Drosophila melanogaster couple to different second messenger pathways. / Ren, Guilin Robin; Folke, Jonas; Hauser, Frank; Li, Shizhong; Grimmelikhuijzen, Cornelis.

In: Biochemical and Biophysical Research Communications, Vol. 462, No. 4, 2015, p. 358-364.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ren, GR, Folke, J, Hauser, F, Li, S & Grimmelikhuijzen, C 2015, 'The A- and B-type muscarinic acetylcholine receptors from Drosophila melanogaster couple to different second messenger pathways', Biochemical and Biophysical Research Communications, vol. 462, no. 4, pp. 358-364. https://doi.org/10.1016/j.bbrc.2015.04.141

APA

Ren, G. R., Folke, J., Hauser, F., Li, S., & Grimmelikhuijzen, C. (2015). The A- and B-type muscarinic acetylcholine receptors from Drosophila melanogaster couple to different second messenger pathways. Biochemical and Biophysical Research Communications, 462(4), 358-364. https://doi.org/10.1016/j.bbrc.2015.04.141

Vancouver

Ren GR, Folke J, Hauser F, Li S, Grimmelikhuijzen C. The A- and B-type muscarinic acetylcholine receptors from Drosophila melanogaster couple to different second messenger pathways. Biochemical and Biophysical Research Communications. 2015;462(4):358-364. https://doi.org/10.1016/j.bbrc.2015.04.141

Author

Ren, Guilin Robin ; Folke, Jonas ; Hauser, Frank ; Li, Shizhong ; Grimmelikhuijzen, Cornelis. / The A- and B-type muscarinic acetylcholine receptors from Drosophila melanogaster couple to different second messenger pathways. In: Biochemical and Biophysical Research Communications. 2015 ; Vol. 462, No. 4. pp. 358-364.

Bibtex

@article{4d6a8ef516344bb88f51b1af047e2a9b,
title = "The A- and B-type muscarinic acetylcholine receptors from Drosophila melanogaster couple to different second messenger pathways",
abstract = "Muscarinic acetylcholine receptors (mAChRs) are G protein-coupled receptors (GPCRs) that are activated by the agonists acetylcholine and muscarine and blocked by several antagonists, among them atropine. In mammals five mAChRs (m1-m5) exist of which m1, m3, and m5 are coupled to members of the Gq/11 family and m2 and m4 to members of the Gi/0 family. We have recently shown that Drosophila melanogaster and other arthropods have two mAChRs, named A and B, where the A-type has the same pharmacology as the mammalian mAChRs, while the B-type has a very low affinity to muscarine and no affinity to classical antagonists such as atropine. Here, we find that the D. melanogaster A-type mAChR is coupled to Gq/11 and D. melanogaster B-type mAChR to Gi/0. Furthermore, by comparing the second and third intracellular loops of all animal mAChRs for which the G protein coupling has been established, we could identify several amino acid residues likely to be specific for either Gq/11 or Gi/0 coupling. Using these hallmarks for specific mAChR G protein interaction we found that all protostomes with a sequenced genome have one mAChR coupled to Gq/11 and one to four mAChRs coupled to Gi/0. Furthermore, in protostomes, probably all A-type mAChRs are coupled to Gq/11 and all B-type mAChRs to G0/i.",
author = "Ren, {Guilin Robin} and Jonas Folke and Frank Hauser and Shizhong Li and Cornelis Grimmelikhuijzen",
note = "Copyright {\textcopyright} 2015. Published by Elsevier Inc.",
year = "2015",
doi = "10.1016/j.bbrc.2015.04.141",
language = "English",
volume = "462",
pages = "358--364",
journal = "Biochemical and Biophysical Research Communications",
issn = "0006-291X",
publisher = "Elsevier",
number = "4",

}

RIS

TY - JOUR

T1 - The A- and B-type muscarinic acetylcholine receptors from Drosophila melanogaster couple to different second messenger pathways

AU - Ren, Guilin Robin

AU - Folke, Jonas

AU - Hauser, Frank

AU - Li, Shizhong

AU - Grimmelikhuijzen, Cornelis

N1 - Copyright © 2015. Published by Elsevier Inc.

PY - 2015

Y1 - 2015

N2 - Muscarinic acetylcholine receptors (mAChRs) are G protein-coupled receptors (GPCRs) that are activated by the agonists acetylcholine and muscarine and blocked by several antagonists, among them atropine. In mammals five mAChRs (m1-m5) exist of which m1, m3, and m5 are coupled to members of the Gq/11 family and m2 and m4 to members of the Gi/0 family. We have recently shown that Drosophila melanogaster and other arthropods have two mAChRs, named A and B, where the A-type has the same pharmacology as the mammalian mAChRs, while the B-type has a very low affinity to muscarine and no affinity to classical antagonists such as atropine. Here, we find that the D. melanogaster A-type mAChR is coupled to Gq/11 and D. melanogaster B-type mAChR to Gi/0. Furthermore, by comparing the second and third intracellular loops of all animal mAChRs for which the G protein coupling has been established, we could identify several amino acid residues likely to be specific for either Gq/11 or Gi/0 coupling. Using these hallmarks for specific mAChR G protein interaction we found that all protostomes with a sequenced genome have one mAChR coupled to Gq/11 and one to four mAChRs coupled to Gi/0. Furthermore, in protostomes, probably all A-type mAChRs are coupled to Gq/11 and all B-type mAChRs to G0/i.

AB - Muscarinic acetylcholine receptors (mAChRs) are G protein-coupled receptors (GPCRs) that are activated by the agonists acetylcholine and muscarine and blocked by several antagonists, among them atropine. In mammals five mAChRs (m1-m5) exist of which m1, m3, and m5 are coupled to members of the Gq/11 family and m2 and m4 to members of the Gi/0 family. We have recently shown that Drosophila melanogaster and other arthropods have two mAChRs, named A and B, where the A-type has the same pharmacology as the mammalian mAChRs, while the B-type has a very low affinity to muscarine and no affinity to classical antagonists such as atropine. Here, we find that the D. melanogaster A-type mAChR is coupled to Gq/11 and D. melanogaster B-type mAChR to Gi/0. Furthermore, by comparing the second and third intracellular loops of all animal mAChRs for which the G protein coupling has been established, we could identify several amino acid residues likely to be specific for either Gq/11 or Gi/0 coupling. Using these hallmarks for specific mAChR G protein interaction we found that all protostomes with a sequenced genome have one mAChR coupled to Gq/11 and one to four mAChRs coupled to Gi/0. Furthermore, in protostomes, probably all A-type mAChRs are coupled to Gq/11 and all B-type mAChRs to G0/i.

U2 - 10.1016/j.bbrc.2015.04.141

DO - 10.1016/j.bbrc.2015.04.141

M3 - Journal article

C2 - 25964087

VL - 462

SP - 358

EP - 364

JO - Biochemical and Biophysical Research Communications

JF - Biochemical and Biophysical Research Communications

SN - 0006-291X

IS - 4

ER -

ID: 137422818