The anophelins are small protein thrombin inhibitors that are produced in the salivary glands of the 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 . To test this prediction, insect cell expression of two anophelin proteins, from and , 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 exhibiting a 100-fold increase in potency compared with the unmodified homologue. Sulfated anophelins were also shown to exhibit potent anticoagulant and antithrombotic activity.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920608 | PMC |
http://dx.doi.org/10.1021/acscentsci.7b00612 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!