Dyckes D F, Kini H, Sheppard R C
Int J Pept Protein Res. 1977;9(5):340-8. doi: 10.1111/j.1399-3011.1977.tb03497.x.
Treatment of basic pancreatic trypsin inhibitor (BPTI, I) with cyanogen bromide smoothly yields the chain cleaved derivative II. The utility of the seco-lactone (II) in the partial synthesis of protein analogues has been investigated. It is shown that the homoserine lactone ring is sufficiently reactive to combine directly with the radiolabelled synthetic peptide glycylglycylanine t-butyl ester in both aqueous and non-aqueous solution, leading to a BPTI analogue which has been purified and characterized.
用溴化氰处理碱性胰蛋白酶抑制剂(BPTI,I)可顺利得到链裂解衍生物II。已对该开环内酯(II)在蛋白质类似物的部分合成中的效用进行了研究。结果表明,高丝氨酸内酯环具有足够的反应活性,可在水溶液和非水溶液中直接与放射性标记的合成肽甘氨酰甘氨酰丙氨酸叔丁酯结合,从而得到一种已被纯化和表征的BPTI类似物。