Yang K H, Fang H, Ye J S, Gong J Z, Wang J T, Xu W F
School of Pharmaceutical Sciences, Shandong University, Ji'nan, P.R. China.
Pharmazie. 2008 Nov;63(11):779-83.
Gram negative bacteria-derived and synthetic N-formyl peptides play a key role in host defense as chemotactic factors for phagocytic leukocytes. The first compound to be identified was N-formylmethionyl-leucyl-phenylalanine (fMLP) which contains highly potent leukocyte chemoattractant. Natural fMLP was subsequently purified and identified in supernatants of gram negative bacteria. Recently, much more attention has been focused on the human formyl peptide receptor (FPR) and its variant formyl peptide receptor-like 1 (FPRL1) and formyl peptide receptor-like 2 (FPRL2). Chemotactic factors such as fMLP interact with their specific cell surface receptors, which results in multiple biological responses through a G protein-coupled signal pathway. In this review, the functions and structural modifications of fMLP are discussed in view of future drug development.
革兰氏阴性菌衍生的和合成的N-甲酰基肽作为吞噬性白细胞的趋化因子,在宿主防御中发挥关键作用。第一个被鉴定出的化合物是N-甲酰基蛋氨酰-亮氨酰-苯丙氨酸(fMLP),它含有高效的白细胞趋化剂。随后,天然fMLP在革兰氏阴性菌的上清液中被纯化和鉴定出来。最近,人们更多地关注人甲酰肽受体(FPR)及其变体甲酰肽受体样1(FPRL1)和甲酰肽受体样2(FPRL2)。诸如fMLP等趋化因子与其特定的细胞表面受体相互作用,通过G蛋白偶联信号通路产生多种生物学反应。在这篇综述中,鉴于未来的药物开发,对fMLP的功能和结构修饰进行了讨论。