Ivanovski G, Copic A, Krizaj I, Gubensek F, Pungercar J
Department of Biochemistry and Molecular Biology, Jozef Stefan Institute, Jamova 39, Ljubljana, SI-1000, Slovenia.
Biochem Biophys Res Commun. 2000 Oct 5;276(3):1229-34. doi: 10.1006/bbrc.2000.3605.
Quadruple (Y115K/I116K/R118M/N119L) and double (Y115K/I116K) mutants of ammodytoxin A, a presynaptically toxic phospholipase A(2) from Vipera ammodytes ammodytes venom, were prepared and characterized. The enzymatic activity of the quadruple mutant on phosphatidylcholine micelles was threefold higher than that of AtxA, presumably due to higher phospholipid-binding affinity, whereas the activity of the double mutant was twofold lower. The substantial decrease by more than two orders of magnitude in the lethal potency of both mutants, together with their decreased binding affinity for neuronal receptors, indicates involvement of the amino acid region 115-119 in neurotoxicity. The similar decrease of toxicity for the two mutants points to the importance of the residues Y115 and I116.
制备并表征了来自极北蝰毒液的突触前毒性磷脂酶A₂——锯鳞蝰毒素A的四重突变体(Y115K/I116K/R118M/N119L)和双重突变体(Y115K/I116K)。四重突变体对磷脂酰胆碱微团的酶活性比锯鳞蝰毒素A高两倍,这可能是由于其对磷脂的结合亲和力更高,而双重突变体的活性则低两倍。两种突变体的致死效力均大幅下降超过两个数量级,同时它们对神经元受体的结合亲和力也降低,这表明115 - 119氨基酸区域参与了神经毒性。两种突变体毒性的类似下降表明Y115和I116残基的重要性。