Kasheverov I E, Utkin Y N, Franke P, Tsetlin V I
Laboratory of Neuropeptide Receptors, Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia.
J Pept Res. 1997 Dec;50(6):408-14. doi: 10.1111/j.1399-3011.1997.tb01203.x.
Photoactivatable substance P (SP) derivatives containing the p-benzoylbenzoic moiety at the N-terminal alpha-amino group of Arg 1 or at the epsilon-amino group of Lys 3 were prepared. Both derivatives also had a p-hydroxyphenylpropionyl group for radioiodination. To obtain the analogue with the photolabel at Arg 1, SP was first reacted with N-hydroxysuccinimide p-hydroxyphenylpropionate, the Lys 3-modified derivative was isolated by reversed-phase high-performance liquid chromatography (HPLC), reacted with N-hydroxysuccinimide p-benzoylbenzoate and purified by HPLC. To place the photolabel at Lys 3, the order of the reactions was reversed. The structure of the derivatives obtained was confirmed by mass spectrometry. The interaction of the derivatives obtained and of their 125I-labeled forms with the NK-1 neurokinin receptor from the rat brain, as well as with the nicotinic acetylcholine receptor from Torpedo electrocytes was analyzed. The results obtained supported by the data from the literature indicate that benzoylbenzoic acid derivatives should not be considered as universal photolabels, which ensure in all cases a high level of photo-cross-linking.
制备了在精氨酸1的N端α-氨基或赖氨酸3的ε-氨基处含有对苯甲酰基苯甲酸部分的光活化P物质(SP)衍生物。两种衍生物还具有用于放射性碘化的对羟基苯丙酰基。为了获得在精氨酸1处带有光标记的类似物,首先使SP与对羟基苯丙酰基N-羟基琥珀酰亚胺酯反应,通过反相高效液相色谱(HPLC)分离赖氨酸3修饰的衍生物,使其与对苯甲酰基苯甲酸N-羟基琥珀酰亚胺酯反应并通过HPLC纯化。为了将光标记置于赖氨酸3处,反应顺序颠倒。通过质谱法确认所获得的衍生物的结构。分析了所获得的衍生物及其125I标记形式与大鼠脑NK-1神经激肽受体以及来自电鳐电细胞的烟碱型乙酰胆碱受体的相互作用。文献数据支持的结果表明,不应将苯甲酰基苯甲酸衍生物视为通用的光标记,即在所有情况下都能确保高水平的光交联。