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新型靶向 18kDa 转位蛋白的不可逆荧光探针:合成与生物学特性。

Novel irreversible fluorescent probes targeting the 18 kDa translocator protein: synthesis and biological characterization.

机构信息

Dipartimento di Scienze Farmaceutiche, Università di Pisa, Pisa, Italy.

出版信息

J Med Chem. 2010 May 27;53(10):4085-93. doi: 10.1021/jm100100q.

DOI:10.1021/jm100100q
PMID:20438080
Abstract

The 18 kDa translocator protein (TSPO) is a mitochondrial protein whose basal density is altered in several diseases, with the result that the evaluation of its expression levels by means of molecular imaging techniques represents a promising diagnostic approach. Experimental procedures using a labeled ligand often cause loss of the bound probe, and consequently high affinity ligands covalently binding the receptor protein are needed to overcome this problem. We have previously described a series of N,N-dialkyl-(2-phenylindol-3-yl)glyoxylamides as potent and selective TSPO ligands. Starting from these derivatives, we designed novel TSPO irreversible ligands bearing an electrophilic isothiocyanato group (7, 8), together with an irreversible NBD-fluorescent probe (18). The TSPO affinity of the new irreversible ligands was measured on rat tissue homogenates by [(3)H]Ro 5-4864 radiobinding kinetic assays, all compounds showing high affinities for the target protein. Further biological characterization of the fluorescent irreversible TSPO probe 18 was carried out by using fluorescent spectroscopy in human glioma cells.

摘要

18 kDa 转位蛋白(TSPO)是一种线粒体蛋白,其基础密度在几种疾病中发生改变,因此,通过分子影像学技术评估其表达水平是一种很有前途的诊断方法。使用标记配体的实验程序通常会导致结合探针的丢失,因此需要与受体蛋白共价结合的高亲和力配体来克服这个问题。我们之前描述了一系列 N,N-二烷基-(2-苯基吲哚-3-基)乙二酰亚胺作为有效的和选择性的 TSPO 配体。从这些衍生物出发,我们设计了带有亲电异硫氰酸酯基团的新型 TSPO 不可逆配体(7,8),以及不可逆的 NBD-荧光探针(18)。通过 [(3)H]Ro 5-4864 放射性结合动力学测定,在大鼠组织匀浆中测量了新的不可逆配体对 TSPO 的亲和力,所有化合物均显示出对靶蛋白的高亲和力。通过在人神经胶质瘤细胞中进行荧光光谱法,对荧光不可逆 TSPO 探针 18 的进一步生物学特性进行了研究。

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