Ramesh C V, Jayakumar R, Puvanakrishnan R
Department of Biotechnology, Central Leather Research Institute, Adyar, Madras, India.
Int J Pept Protein Res. 1995 Apr;45(4):386-90. doi: 10.1111/j.1399-3011.1995.tb01053.x.
A novel peptide, tert-butyloxycarbonyl-L-arginine-L-proline lauryl ester laurate, synthesised by a solution-phase method, formed micelles in aqueous solutions and was observed to exhibit anticoagulant activity as shown by clotting assays such as the thrombin time (TT) test, the prothrombin time (PT) test and the activated partial thromboplastin time (APTT) test. TT and PT were found to be normal up to a particular concentration of peptide, and above that level they increased with increasing concentration of peptide, while APTT did not exhibit much significance. Conductometric and potentiometric studies showed that the peptide formed a stable micelle, and the anticoagulant activity of this peptide was also compared with a non-arginine-containing peptide (control) known to form micelles. The anticoagulant action in the micellar form could be due to the inhibition of thrombin, as seen from the decrease in amidolytic activity. The inhibitory activity of the peptide was explained in the light of micelle formation.
一种通过溶液相法合成的新型肽,叔丁氧羰基-L-精氨酸-L-脯氨酸月桂酯月桂酸酯,在水溶液中形成胶束,并且通过凝血试验如凝血酶时间(TT)试验、凝血酶原时间(PT)试验和活化部分凝血活酶时间(APTT)试验显示出抗凝活性。发现直到肽的特定浓度时TT和PT均正常,高于该水平时它们随肽浓度的增加而增加,而APTT没有表现出太大意义。电导和电位研究表明该肽形成了稳定的胶束,并且还将该肽的抗凝活性与已知形成胶束的不含精氨酸的肽(对照)进行了比较。从酰胺水解活性的降低可以看出,胶束形式的抗凝作用可能是由于对凝血酶的抑制。根据胶束形成解释了该肽的抑制活性。