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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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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. |
format | Online Article Text |
id | pubmed-5920608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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