Gaudriault G, Vincent J P
Institut de Pharmacologie Moléculaire et Cellulaire, UPR 411 CNRS, Valbonne, France.
Peptides. 1992 Nov-Dec;13(6):1187-92. doi: 10.1016/0196-9781(92)90027-z.
Incorporation of N-succinimidyl-3(4-hydroxyphenyl) propionate (Bolton-Hunter reagent) or its 125I-labeled derivative into peptides can be selectively directed towards either alpha- or epsilon-amine functions by modifying the pH of the reaction. Acylation of alpha-amino groups is favored at pH 6.5 whereas epsilon-amino groups react more readily at pH 8.5. We have taken advantage of this result to prepare two new 125I-labeled analogues of substance P and neurotensin that bind selectively and reversibly to their respective receptors. The method described here is of general interest and can be used to incorporate various reporter groups into peptide structures.
通过改变反应的pH值,可将N-琥珀酰亚胺基-3(4-羟苯基)丙酸酯(博尔顿-亨特试剂)或其125I标记的衍生物选择性地引入肽的α-或ε-氨基官能团。在pH 6.5时,α-氨基的酰化反应更有利,而在pH 8.5时,ε-氨基反应更迅速。我们利用这一结果制备了两种新的125I标记的P物质和神经降压素类似物,它们能选择性且可逆地与其各自的受体结合。本文所述方法具有普遍意义,可用于将各种报告基团引入肽结构中。