Shina R, Rosenberg P, Condrea E
Felsenstein Medical Research Center, Petah Tikva, Israel.
Toxicon. 1992 Nov;30(11):1501-4. doi: 10.1016/0041-0101(92)90529-e.
An EDTA.Ca2+ complex inhibits the phospholipase A2 activity of the presynaptic neurotoxin beta-bungarotoxin without affecting its lethal potency. The EDTA.Ca2+ complex induces a conformational change in the enzymatic active site region of beta-BuTx, as indicated by the suppression of the 340 nm tryptophan fluorescence peak. Modification of the enzymatic site without loss of toxicity supports the presence of separate loci for the two activities.
乙二胺四乙酸钙(EDTA.Ca2+)复合物可抑制突触前神经毒素β-银环蛇毒素的磷脂酶A2活性,而不影响其致死效力。如340nm色氨酸荧光峰的抑制所示,EDTA.Ca2+复合物诱导β-银环蛇毒素(β-BuTx)酶活性位点区域发生构象变化。酶活性位点的修饰而不丧失毒性,支持了这两种活性存在独立位点。