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Mosquito-Derived Anophelin Sulfoproteins Are Potent Antithrombotics

[Image: see text] The anophelins are small protein thrombin inhibitors that are produced in the salivary glands of the Anopheles mosquito to fulfill a vital role in blood feeding. A bioinformatic analysis of anophelin sequences revealed the presence of conserved tyrosine residues in an acidic enviro...

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Autores principales: Watson, Emma E., Liu, Xuyu, Thompson, Robert E., Ripoll-Rozada, Jorge, Wu, Mike, Alwis, Imala, Gori, Alessandro, Loh, Choy-Theng, Parker, Benjamin L., Otting, Gottfried, Jackson, Shaun, Pereira, Pedro José Barbosa, Payne, Richard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920608/
https://www.ncbi.nlm.nih.gov/pubmed/29721529
http://dx.doi.org/10.1021/acscentsci.7b00612
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author Watson, Emma E.
Liu, Xuyu
Thompson, Robert E.
Ripoll-Rozada, Jorge
Wu, Mike
Alwis, Imala
Gori, Alessandro
Loh, Choy-Theng
Parker, Benjamin L.
Otting, Gottfried
Jackson, Shaun
Pereira, Pedro José Barbosa
Payne, Richard J.
author_facet Watson, Emma E.
Liu, Xuyu
Thompson, Robert E.
Ripoll-Rozada, Jorge
Wu, Mike
Alwis, Imala
Gori, Alessandro
Loh, Choy-Theng
Parker, Benjamin L.
Otting, Gottfried
Jackson, Shaun
Pereira, Pedro José Barbosa
Payne, Richard J.
author_sort Watson, Emma E.
collection PubMed
description [Image: see text] The anophelins are small protein thrombin inhibitors that are produced in the salivary glands of the Anopheles mosquito to fulfill a vital role in blood feeding. A bioinformatic analysis of anophelin sequences revealed the presence of conserved tyrosine residues in an acidic environment that were predicted to be post-translationally sulfated in vivo. To test this prediction, insect cell expression of two anophelin proteins, from Anopheles albimanus and Anopheles gambiae, was performed, followed by analysis by mass spectrometry, which showed heterogeneous sulfation at the predicted sites. Homogeneously sulfated variants of the two proteins were subsequently generated by chemical synthesis via a one-pot ligation–desulfurization strategy. Tyrosine sulfation of the anophelins was shown to significantly enhance the thrombin inhibitory activity, with a doubly sulfated variant of the anophelin from A. albimanus exhibiting a 100-fold increase in potency compared with the unmodified homologue. Sulfated anophelins were also shown to exhibit potent in vivo anticoagulant and antithrombotic activity.
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spelling pubmed-59206082018-05-02 Mosquito-Derived Anophelin Sulfoproteins Are Potent Antithrombotics Watson, Emma E. Liu, Xuyu Thompson, Robert E. Ripoll-Rozada, Jorge Wu, Mike Alwis, Imala Gori, Alessandro Loh, Choy-Theng Parker, Benjamin L. Otting, Gottfried Jackson, Shaun Pereira, Pedro José Barbosa Payne, Richard J. ACS Cent Sci [Image: see text] The anophelins are small protein thrombin inhibitors that are produced in the salivary glands of the Anopheles mosquito to fulfill a vital role in blood feeding. A bioinformatic analysis of anophelin sequences revealed the presence of conserved tyrosine residues in an acidic environment that were predicted to be post-translationally sulfated in vivo. To test this prediction, insect cell expression of two anophelin proteins, from Anopheles albimanus and Anopheles gambiae, was performed, followed by analysis by mass spectrometry, which showed heterogeneous sulfation at the predicted sites. Homogeneously sulfated variants of the two proteins were subsequently generated by chemical synthesis via a one-pot ligation–desulfurization strategy. Tyrosine sulfation of the anophelins was shown to significantly enhance the thrombin inhibitory activity, with a doubly sulfated variant of the anophelin from A. albimanus exhibiting a 100-fold increase in potency compared with the unmodified homologue. Sulfated anophelins were also shown to exhibit potent in vivo anticoagulant and antithrombotic activity. American Chemical Society 2018-03-28 2018-04-25 /pmc/articles/PMC5920608/ /pubmed/29721529 http://dx.doi.org/10.1021/acscentsci.7b00612 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Watson, Emma E.
Liu, Xuyu
Thompson, Robert E.
Ripoll-Rozada, Jorge
Wu, Mike
Alwis, Imala
Gori, Alessandro
Loh, Choy-Theng
Parker, Benjamin L.
Otting, Gottfried
Jackson, Shaun
Pereira, Pedro José Barbosa
Payne, Richard J.
Mosquito-Derived Anophelin Sulfoproteins Are Potent Antithrombotics
title Mosquito-Derived Anophelin Sulfoproteins Are Potent Antithrombotics
title_full Mosquito-Derived Anophelin Sulfoproteins Are Potent Antithrombotics
title_fullStr Mosquito-Derived Anophelin Sulfoproteins Are Potent Antithrombotics
title_full_unstemmed Mosquito-Derived Anophelin Sulfoproteins Are Potent Antithrombotics
title_short Mosquito-Derived Anophelin Sulfoproteins Are Potent Antithrombotics
title_sort mosquito-derived anophelin sulfoproteins are potent antithrombotics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920608/
https://www.ncbi.nlm.nih.gov/pubmed/29721529
http://dx.doi.org/10.1021/acscentsci.7b00612
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