| Literature DB >> 24183721 |
Chandrasekhar Chanda1, Angshuman Sarkar, Srinivas Sistla, Dibakar Chakrabarty.
Abstract
A low molecular weight anti-platelet peptide (6.9 kDa) has been purified from Naja kaouthia venom and was named KT-6.9. MALDI-TOF/TOF mass spectrometry analysis revealed the homology of KT-6.9 peptide sequence with many three finger toxin family members. KT-6.9 inhibited human platelet aggregation process in a dose dependent manner. It has inhibited ADP, thrombin and arachidonic acid induced platelet aggregation process in dose dependent manner, but did not inhibit collagen and ristocetin induced platelet aggregation. Strong inhibition (70%) of the ADP induced platelet aggregation by KT-6.9 suggests competition with ADP for its receptors on platelet surface. Anti-platelet activity of KT-6.9 was found to be 25 times stronger than that of anti-platelet drug clopidogrel. Binding of KT-6.9 to platelet surface was confirmed by surface plasma resonance analysis using BIAcore X100. Binding was also observed by a modified sandwich ELISA method using anti-KT-6.9 antibodies. KT-6.9 is probably the first 3 FTx from Indian monocled cobra venom reported as a platelet aggregation inhibitor.Entities:
Keywords: 3FTx; ADP; Anti-platelet; FITC; G-protein coupled receptor; GPCR; Indian cobra venom; KT-6.9; MW; P2Y receptor; RP-HPLC; SPR; adenosine di-phosphate; fluorescein isothiocyanate; molecular weight; reversed phase high performance liquid chromatography; surface plasma resonance
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Year: 2013 PMID: 24183721 DOI: 10.1016/j.bbrc.2013.10.125
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575