Selective Negative Allosteric Modulation Of Metabotropic Glutamate Receptors - A Structural Perspective of Ligands and Mutants

Research output: Contribution to journalJournal articleResearchpeer-review

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Selective Negative Allosteric Modulation Of Metabotropic Glutamate Receptors - A Structural Perspective of Ligands and Mutants. / Harpsøe, Kasper; Isberg, Vignir; Tehan, Benjamin G; Weiss, Dahlia; Arsova, Angela; Marshall, Fiona H; Bräuner-Osborne, Hans; Gloriam, David E.

In: Scientific Reports, Vol. 5, 13869, 11.09.2015, p. 1-11.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Harpsøe, K, Isberg, V, Tehan, BG, Weiss, D, Arsova, A, Marshall, FH, Bräuner-Osborne, H & Gloriam, DE 2015, 'Selective Negative Allosteric Modulation Of Metabotropic Glutamate Receptors - A Structural Perspective of Ligands and Mutants' Scientific Reports, vol. 5, 13869, pp. 1-11. https://doi.org/10.1038/srep13869

APA

Harpsøe, K., Isberg, V., Tehan, B. G., Weiss, D., Arsova, A., Marshall, F. H., ... Gloriam, D. E. (2015). Selective Negative Allosteric Modulation Of Metabotropic Glutamate Receptors - A Structural Perspective of Ligands and Mutants. Scientific Reports, 5, 1-11. [13869]. https://doi.org/10.1038/srep13869

Vancouver

Harpsøe K, Isberg V, Tehan BG, Weiss D, Arsova A, Marshall FH et al. Selective Negative Allosteric Modulation Of Metabotropic Glutamate Receptors - A Structural Perspective of Ligands and Mutants. Scientific Reports. 2015 Sep 11;5:1-11. 13869. https://doi.org/10.1038/srep13869

Author

Harpsøe, Kasper ; Isberg, Vignir ; Tehan, Benjamin G ; Weiss, Dahlia ; Arsova, Angela ; Marshall, Fiona H ; Bräuner-Osborne, Hans ; Gloriam, David E. / Selective Negative Allosteric Modulation Of Metabotropic Glutamate Receptors - A Structural Perspective of Ligands and Mutants. In: Scientific Reports. 2015 ; Vol. 5. pp. 1-11.

Bibtex

@article{cfb1519ade1c498ea44d6c773b3fe0fd,
title = "Selective Negative Allosteric Modulation Of Metabotropic Glutamate Receptors - A Structural Perspective of Ligands and Mutants",
abstract = "The metabotropic glutamate receptors have a wide range of modulatory functions in the central nervous system. They are among the most highly pursued drug targets, with relevance for several neurological diseases, and a number of allosteric modulators have entered clinical trials. However, so far this has not led to a marketed drug, largely because of the difficulties in achieving subtype-selective compounds with desired properties. Very recently the first crystal structures were published for the transmembrane domain of two metabotropic glutamate receptors in complex with negative allosteric modulators. In this analysis, we make the first comprehensive structural comparison of all metabotropic glutamate receptors, placing selective negative allosteric modulators and critical mutants into the detailed context of the receptor binding sites. A better understanding of how the different mGlu allosteric modulator binding modes relates to selective pharmacological actions will be very valuable for rational design of safer drugs.",
author = "Kasper Harps{\o}e and Vignir Isberg and Tehan, {Benjamin G} and Dahlia Weiss and Angela Arsova and Marshall, {Fiona H} and Hans Br{\"a}uner-Osborne and Gloriam, {David E}",
year = "2015",
month = "9",
day = "11",
doi = "10.1038/srep13869",
language = "English",
volume = "5",
pages = "1--11",
journal = "Scientific Reports",
issn = "2045-2322",
publisher = "nature publishing group",

}

RIS

TY - JOUR

T1 - Selective Negative Allosteric Modulation Of Metabotropic Glutamate Receptors - A Structural Perspective of Ligands and Mutants

AU - Harpsøe, Kasper

AU - Isberg, Vignir

AU - Tehan, Benjamin G

AU - Weiss, Dahlia

AU - Arsova, Angela

AU - Marshall, Fiona H

AU - Bräuner-Osborne, Hans

AU - Gloriam, David E

PY - 2015/9/11

Y1 - 2015/9/11

N2 - The metabotropic glutamate receptors have a wide range of modulatory functions in the central nervous system. They are among the most highly pursued drug targets, with relevance for several neurological diseases, and a number of allosteric modulators have entered clinical trials. However, so far this has not led to a marketed drug, largely because of the difficulties in achieving subtype-selective compounds with desired properties. Very recently the first crystal structures were published for the transmembrane domain of two metabotropic glutamate receptors in complex with negative allosteric modulators. In this analysis, we make the first comprehensive structural comparison of all metabotropic glutamate receptors, placing selective negative allosteric modulators and critical mutants into the detailed context of the receptor binding sites. A better understanding of how the different mGlu allosteric modulator binding modes relates to selective pharmacological actions will be very valuable for rational design of safer drugs.

AB - The metabotropic glutamate receptors have a wide range of modulatory functions in the central nervous system. They are among the most highly pursued drug targets, with relevance for several neurological diseases, and a number of allosteric modulators have entered clinical trials. However, so far this has not led to a marketed drug, largely because of the difficulties in achieving subtype-selective compounds with desired properties. Very recently the first crystal structures were published for the transmembrane domain of two metabotropic glutamate receptors in complex with negative allosteric modulators. In this analysis, we make the first comprehensive structural comparison of all metabotropic glutamate receptors, placing selective negative allosteric modulators and critical mutants into the detailed context of the receptor binding sites. A better understanding of how the different mGlu allosteric modulator binding modes relates to selective pharmacological actions will be very valuable for rational design of safer drugs.

U2 - 10.1038/srep13869

DO - 10.1038/srep13869

M3 - Journal article

VL - 5

SP - 1

EP - 11

JO - Scientific Reports

JF - Scientific Reports

SN - 2045-2322

M1 - 13869

ER -

ID: 144697865