Zhu H, Bussey H, Thomas D Y, Gagnon J, Bell A W
J Biol Chem. 1987 Aug 5;262(22):10728-32.
The carboxyl-terminal sequences of the two polypeptide chains of the Saccharomyces cerevisiae K1 killer toxin were determined by protein sequencing and amino acid analysis of peptide fragments generated from the mature, secreted toxin. The COOH-terminal amino acid of the beta chain is histidine 316, the final residue encoded by the precursor gene. The COOH terminus of the alpha chain is at alanine 147 of the preprotoxin. Amino acid composition data for the purified toxin are consistent with that predicted from the gene sequence of the preprotoxin where the alpha and beta subunits consist of amino acid residues 45-147 and 234-316, respectively. The molecular weight of the mature alpha beta dimer is about 20,658. The COOH-terminal sequence determination completes the location of the toxin subunits in the precursor, and its configuration may be represented as prepropeptide-Pro-Arg-alpha-Arg-Arg-gamma-Lys-Arg-beta, where gamma represents the interstitial glycosylated peptide. The COOH terminal side of the paired basic residues (Arg-148 Arg-149 and Lys-232 Arg-233 of preprotoxin) are endoproteolytic processing sites for the product of the KEX2 gene (Julius, D., Brake, A., Blair, L., Kunisawa, R., and Thorner, J. (1984) Cell 37, 1075-1089), and thus maturation of the alpha subunit of killer toxin apparently requires a carboxypeptidase B-like activity. A possible candidate for this activity is the product of the KEX1 gene (Dmochowska, A., Dignard, D., Henning, D., Thomas, D.Y., and Bussey, H. (1987) Cell, in press).
通过对从成熟分泌毒素产生的肽片段进行蛋白质测序和氨基酸分析,确定了酿酒酵母K1杀伤毒素两条多肽链的羧基末端序列。β链的羧基末端氨基酸是组氨酸316,这是前体基因编码的最后一个残基。α链的羧基末端位于前原毒素的丙氨酸147处。纯化毒素的氨基酸组成数据与从前原毒素基因序列预测的数据一致,其中α和β亚基分别由氨基酸残基45 - 147和234 - 316组成。成熟αβ二聚体的分子量约为20,658。羧基末端序列的确定完成了毒素亚基在前体中的定位,其构型可表示为前原肽 - 脯氨酸 - 精氨酸 - α - 精氨酸 - 精氨酸 - γ - 赖氨酸 - 精氨酸 - β,其中γ代表中间糖基化肽。成对碱性残基(前原毒素的精氨酸 - 148、精氨酸 - 149和赖氨酸 - 232、精氨酸 - 233)的羧基末端侧是KEX2基因产物的内蛋白水解加工位点(朱利叶斯,D.,布雷克,A.,布莱尔,L.,久保泽,R.,和索纳,J.(1984年)《细胞》37卷,1075 - 1089页),因此杀伤毒素α亚基的成熟显然需要一种羧肽酶B样活性。这种活性的一个可能候选者是KEX1基因的产物(德莫乔夫斯卡,A.,迪尼亚德,D.,亨宁,D.,托马斯,D.Y.,和布西,H.(1987年)《细胞》,即将发表)。