6nan
From Proteopedia
NMR structure determination of Ixolaris and Factor X interaction reveals a noncanonical mechanism of Kunitz inhibition
Structural highlights
FunctionIXOSP_IXOSC Anticoagulant protein that modulates blood feeding of ticks on vertebrate species (PubMed:16807644, PubMed:32394234). Inhibits activation of host blood coagulation factor X (F10) (PubMed:11986214, PubMed:18042685, PubMed:28734839). Inhibits activity of host coagulation factor VIIa-tissue factor (F7-F3) complex in a factor X/Xa-dependent manner (PubMed:11986214). Prevents interaction between host coagulation factor X and activated factor VIIIa (F8) (PubMed:18042685).[1] [2] [3] [4] [5] Publication Abstract from PubMedIxolaris is a potent tick salivary anticoagulant that binds coagulation factor Xa (FXa) and zymogen FX, with formation of a quaternary Tissue Factor (TF)/FVIIa/ FX(a)/Ixolaris inhibitory complex. Ixolaris blocks TF-induced coagulation and PAR2 signaling and prevents thrombosis, tumor growth and immune activation. We present a high-resolution structure and dynamics of Ixolaris and describe the structural basis for recognition of FX. Ixolaris consists of two Kunitz domains (K1 and K2) in which K2 is strikingly dynamic and encompasses several residues involved in FX binding. This indicates that the backbone plasticity of K2 is critical for Ixolaris biological activity. Notably, NMR-derived model reveals a mechanism for an electrostatically guided, high-affinity interaction between Ixolaris and FX heparin-binding (pro)exosite, resulting in allosteric switch in the catalytic site. This is the first report revealing the structure-function relationship of an anticoagulant targeting a zymogen serving as a scaffold for TF inhibition. NMR structure determination of Ixolaris and Factor X interaction reveals a noncanonical mechanism of Kunitz inhibition.,De Paula VS, Sgourakis NG, Francischetti IMB, Almeida FCL, Monteiro RQ Prof, Valente AP Blood. 2019 May 27. pii: blood.2018889493. doi: 10.1182/blood.2018889493. PMID:31133602[6] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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