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Dihydroisoxazole inhibitors of Anopheles gambiae seminal transglutaminase AgTG3

BACKGROUND: Current vector-based malaria control strategies are threatened by the rise of biochemical and behavioural resistance in mosquitoes. Researching mosquito traits of immunity and fertility is required to find potential targets for new vector control strategies. The seminal transglutaminase...

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Autores principales: Le, Binh V, Klöck, Cornelius, Schatz, Alexandra, Nguyen, Jennifer B, Kakani, Evdoxia G, Catteruccia, Flaminia, Khosla, Chaitan, Baxter, Richard HG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113009/
https://www.ncbi.nlm.nih.gov/pubmed/24888439
http://dx.doi.org/10.1186/1475-2875-13-210
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author Le, Binh V
Klöck, Cornelius
Schatz, Alexandra
Nguyen, Jennifer B
Kakani, Evdoxia G
Catteruccia, Flaminia
Khosla, Chaitan
Baxter, Richard HG
author_facet Le, Binh V
Klöck, Cornelius
Schatz, Alexandra
Nguyen, Jennifer B
Kakani, Evdoxia G
Catteruccia, Flaminia
Khosla, Chaitan
Baxter, Richard HG
author_sort Le, Binh V
collection PubMed
description BACKGROUND: Current vector-based malaria control strategies are threatened by the rise of biochemical and behavioural resistance in mosquitoes. Researching mosquito traits of immunity and fertility is required to find potential targets for new vector control strategies. The seminal transglutaminase AgTG3 coagulates male Anopheles gambiae seminal fluids, forming a ‘mating plug’ that is required for male reproductive success. Inhibitors of AgTG3 can be useful both as chemical probes of A. gambiae reproductive biology and may further the development of new chemosterilants for mosquito population control. METHODS: A targeted library of 3-bromo-4,5-dihydroxoisoxazole inhibitors were synthesized and screened for inhibition of AgTG3 in a fluorescent, plate-based assay. Positive hits were tested for in vitro activity using cross-linking and mass spectrometry, and in vivo efficacy in laboratory mating assays. RESULTS: A targeted chemical library was screened for inhibition of AgTG3 in a fluorescent plate-based assay using its native substrate, plugin. Several inhibitors were identified with IC(50) < 10 μM. Preliminary structure-activity relationships within the library support the stereo-specificity and preference for aromatic substituents in the chemical scaffold. Both inhibition of plugin cross-linking and covalent modification of the active site cysteine of AgTG3 were verified. Administration of an AgTG3 inhibitor to A. gambiae males by intrathoracic injection led to a 15% reduction in mating plug transfer in laboratory mating assays. CONCLUSIONS: A targeted screen has identified chemical inhibitors of A. gambiae transglutaminase 3 (AgTG3). The most potent inhibitors are known inhibitors of human transglutaminase 2, suggesting a common binding pose may exist within the active site of both enzymes. Future efforts to develop additional inhibitors will provide chemical tools to address important biological questions regarding the role of the A. gambiae mating plug. A second use for transglutaminase inhibitors exists for the study of haemolymph coagulation and immune responses to wound healing in insects.
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spelling pubmed-41130092014-08-05 Dihydroisoxazole inhibitors of Anopheles gambiae seminal transglutaminase AgTG3 Le, Binh V Klöck, Cornelius Schatz, Alexandra Nguyen, Jennifer B Kakani, Evdoxia G Catteruccia, Flaminia Khosla, Chaitan Baxter, Richard HG Malar J Research BACKGROUND: Current vector-based malaria control strategies are threatened by the rise of biochemical and behavioural resistance in mosquitoes. Researching mosquito traits of immunity and fertility is required to find potential targets for new vector control strategies. The seminal transglutaminase AgTG3 coagulates male Anopheles gambiae seminal fluids, forming a ‘mating plug’ that is required for male reproductive success. Inhibitors of AgTG3 can be useful both as chemical probes of A. gambiae reproductive biology and may further the development of new chemosterilants for mosquito population control. METHODS: A targeted library of 3-bromo-4,5-dihydroxoisoxazole inhibitors were synthesized and screened for inhibition of AgTG3 in a fluorescent, plate-based assay. Positive hits were tested for in vitro activity using cross-linking and mass spectrometry, and in vivo efficacy in laboratory mating assays. RESULTS: A targeted chemical library was screened for inhibition of AgTG3 in a fluorescent plate-based assay using its native substrate, plugin. Several inhibitors were identified with IC(50) < 10 μM. Preliminary structure-activity relationships within the library support the stereo-specificity and preference for aromatic substituents in the chemical scaffold. Both inhibition of plugin cross-linking and covalent modification of the active site cysteine of AgTG3 were verified. Administration of an AgTG3 inhibitor to A. gambiae males by intrathoracic injection led to a 15% reduction in mating plug transfer in laboratory mating assays. CONCLUSIONS: A targeted screen has identified chemical inhibitors of A. gambiae transglutaminase 3 (AgTG3). The most potent inhibitors are known inhibitors of human transglutaminase 2, suggesting a common binding pose may exist within the active site of both enzymes. Future efforts to develop additional inhibitors will provide chemical tools to address important biological questions regarding the role of the A. gambiae mating plug. A second use for transglutaminase inhibitors exists for the study of haemolymph coagulation and immune responses to wound healing in insects. BioMed Central 2014-06-02 /pmc/articles/PMC4113009/ /pubmed/24888439 http://dx.doi.org/10.1186/1475-2875-13-210 Text en Copyright © 2014 Le et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Le, Binh V
Klöck, Cornelius
Schatz, Alexandra
Nguyen, Jennifer B
Kakani, Evdoxia G
Catteruccia, Flaminia
Khosla, Chaitan
Baxter, Richard HG
Dihydroisoxazole inhibitors of Anopheles gambiae seminal transglutaminase AgTG3
title Dihydroisoxazole inhibitors of Anopheles gambiae seminal transglutaminase AgTG3
title_full Dihydroisoxazole inhibitors of Anopheles gambiae seminal transglutaminase AgTG3
title_fullStr Dihydroisoxazole inhibitors of Anopheles gambiae seminal transglutaminase AgTG3
title_full_unstemmed Dihydroisoxazole inhibitors of Anopheles gambiae seminal transglutaminase AgTG3
title_short Dihydroisoxazole inhibitors of Anopheles gambiae seminal transglutaminase AgTG3
title_sort dihydroisoxazole inhibitors of anopheles gambiae seminal transglutaminase agtg3
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113009/
https://www.ncbi.nlm.nih.gov/pubmed/24888439
http://dx.doi.org/10.1186/1475-2875-13-210
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