Smith S C, McAdam W J, Kemp B E, Morgan F J, Cotton R G
Olive Miller Protein Chemistry Laboratory, Royal Children's Hospital, Parkville, Victoria, Australia.
Biochem J. 1987 Jun 15;244(3):625-31. doi: 10.1042/bj2440625.
Monoclonal antibody PH7 has specificity for the phosphorylated form of the human liver phenylalanine hydroxylase and negligible reactivity towards the dephosphorylated form of the native enzyme by enzyme-linked immunoassay. PH7 binds specifically to the phosphorylated form of the liver enzyme after SDS/polyacrylamide-gel electrophoresis and transfer to nitrocellulose. Competitive blocking assays have been applied in conjunction with reversed-phase h.p.l.c. of purified tryptic fragments of human liver phenylalanine hydroxylase to localize the epitope. The major immunoreactive tryptic peptide cross-reacting with PH7 had an amino acid analysis corresponding to the first 41 amino acids of the human liver phenylalanine hydroxylase sequence and included the serine residue that is thought to be the phosphorylation site. The monoclonal antibody recognized the phosphorylated form of the synthetic decapeptide corresponding to the local phosphorylation-site sequence Gly-Leu-Gly-Arg-Lys-Leu-Ser(P)-Asp-Phe-Gly, but not the dephosphodecapeptide. Thermolysin digestion of the peptide demonstrated the monoclonal antibody bound to the pentapeptide Leu-Ser(P)-Asp-Phe-Gly. Monoclonal antibody PH7 recognized the phosphodecapeptide at concentrations 10(3)-fold higher than with phenylalanine hydroxylase, compared with 10(4)-10(7)-fold higher for other phosphopeptides and phosphoproteins. The results demonstrate that monoclonal antibody PH7 has specificity for the phosphorylated form of phenylalanine hydroxylase at the phosphorylation site.
单克隆抗体PH7对人肝苯丙氨酸羟化酶的磷酸化形式具有特异性,通过酶联免疫测定法对天然酶的去磷酸化形式的反应性可忽略不计。在SDS/聚丙烯酰胺凝胶电泳并转移至硝酸纤维素膜后,PH7特异性结合肝酶的磷酸化形式。竞争性阻断试验已与纯化的人肝苯丙氨酸羟化酶胰蛋白酶片段的反相高效液相色谱法结合使用,以定位表位。与PH7发生交叉反应的主要免疫反应性胰蛋白酶肽的氨基酸分析对应于人肝苯丙氨酸羟化酶序列的前41个氨基酸,并且包括被认为是磷酸化位点的丝氨酸残基。该单克隆抗体识别对应于局部磷酸化位点序列Gly-Leu-Gly-Arg-Lys-Leu-Ser(P)-Asp-Phe-Gly的合成十肽的磷酸化形式,但不识别去磷酸化十肽。该肽的嗜热菌蛋白酶消化表明单克隆抗体与五肽Leu-Ser(P)-Asp-Phe-Gly结合。与其他磷酸肽和磷酸蛋白相比,单克隆抗体PH7识别磷酸化十肽的浓度比识别苯丙氨酸羟化酶的浓度高10³倍,而识别其他磷酸肽和磷酸蛋白的浓度比识别苯丙氨酸羟化酶的浓度高10⁴-10⁷倍。结果表明,单克隆抗体PH7对苯丙氨酸羟化酶在磷酸化位点的磷酸化形式具有特异性。