Conlon J M, Sheehan L
Regul Pept. 1983 Dec;7(4):335-45. doi: 10.1016/0167-0115(83)90105-2.
Substance P is rapidly converted by enzyme(s) in human plasma to des-[Arg1Pro2]-substance P (fragment 3-11) and to des-[Arg1Pro2Lys3Pro4]-substance P (fragment 5-11). These metabolites were isolated by HPLC and partially sequenced. No evidence was obtained for deamidation of substance P in plasma or for the formation of the N-terminal tetrapeptide [Arg-Pro-Lys-Pro]. The data suggest that substance P is metabolized in human plasma by an enzyme with the specificity of dipeptidyl-aminopeptidase IV. Consistent with this hypothesis, the rate of degradation of substance P measured with an antibody directed against the N-terminal region is 2-3-fold greater than measured with a C-terminally directed antibody. The degrading activity of plasma was purified 522-fold and was eluted from a gel filtration column in the molecular weight zone 150 000-170 000 and from a chromatofocusing column in the pH range 4.5 to 5.5.
P物质在人血浆中迅速被酶转化为去-[精氨酸1脯氨酸2]-P物质(片段3 - 11)和去-[精氨酸1脯氨酸2赖氨酸3脯氨酸4]-P物质(片段5 - 11)。这些代谢产物通过高效液相色谱法分离并进行了部分测序。未获得血浆中P物质脱酰胺或形成N端四肽[精氨酸-脯氨酸-赖氨酸-脯氨酸]的证据。数据表明,P物质在人血浆中被一种具有二肽基氨基肽酶IV特异性的酶代谢。与此假设一致,用针对N端区域的抗体测得的P物质降解速率比用针对C端的抗体测得的速率高2至3倍。血浆的降解活性被纯化了522倍,从凝胶过滤柱上在分子量150000 - 170000区域洗脱,从色谱聚焦柱上在pH范围4.5至5.5洗脱。