Journal of Biological Chemistry · 1996 · 84 citations · 34 references
MedicineMolecular BiologyPharmacologyHemostasisMolecular PharmacologyStructural BiologyEnzyme InhibitionLigand BindingPlatelet AdhesionPlatelet AggregationProtein BindingProtein StructureAmino Acid AnalysisGlycoprotein Iib FunctionGlycoprotein Iiia FunctionGlycoprotein StructurePlatelet Aggregation InhibitionPlatelet Membrane GlycoproteinsPlatelet Surface ReceptorsSalivary Glycoproteins
A novel inhibitor of human platelet aggregation, named variabilin, was isolated from salivary glands of the hard tick Dermacentor variabilis using a combination of gel filtration and high pressure liquid chromatography. Variabilin was a potent antagonist of the fibrinogen receptor glycoprotein IIb-IIIa (GPIIb-IIIa; αIIbβ3) and the vitronectin receptor αvβ3. Amino acid sequence analysis by Edman degradation revealed that it has 47 residues, with a molecular weight of 4968.5. Like many other naturally occurring antagonists of GPIIb-IIIa, variabilin contains the RGD (Arg-Gly-Asp) motif. However, unlike the RGD-containing antagonists of GPIIb-IIIa, the RGD sequence of variabilin is not positioned in a loop bracketed by cysteine residues. It has little sequence homology to the other known naturally occurring antagonists of GPIIb-IIIa, including the disintegrins from snakes, decorsin and ornatin from leeches, and disagregin from soft ticks. Variabilin is the first RGD-containing antagonist isolated from ticks. A novel inhibitor of human platelet aggregation, named variabilin, was isolated from salivary glands of the hard tick Dermacentor variabilis using a combination of gel filtration and high pressure liquid chromatography. Variabilin was a potent antagonist of the fibrinogen receptor glycoprotein IIb-IIIa (GPIIb-IIIa; αIIbβ3) and the vitronectin receptor αvβ3. Amino acid sequence analysis by Edman degradation revealed that it has 47 residues, with a molecular weight of 4968.5. Like many other naturally occurring antagonists of GPIIb-IIIa, variabilin contains the RGD (Arg-Gly-Asp) motif. However, unlike the RGD-containing antagonists of GPIIb-IIIa, the RGD sequence of variabilin is not positioned in a loop bracketed by cysteine residues. It has little sequence homology to the other known naturally occurring antagonists of GPIIb-IIIa, including the disintegrins from snakes, decorsin and ornatin from leeches, and disagregin from soft ticks. Variabilin is the first RGD-containing antagonist isolated from ticks.
34
The platelet membrane glycoprotein IIb-IIIa complex
IF Charo, LV Parise, LA Fitzgerald · Blood · 1988 · 1K citations · Full text
Medicine, Biochemistry, Hematology +14
The platelet membrane glycoprotein IIb-IIIa complex
DR Phillips, IF Charo, LV Parise et al. · Blood · 1988 · 879 citations · Full text
Medicine, Biochemistry, Hematology +14