Graduate School of Medicine, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
PRESTO Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama, 332-0012, Japan.
Angew Chem Int Ed Engl. 2021 Jan 25;60(4):2125-2129. doi: 10.1002/anie.202013265. Epub 2020 Nov 23.
γ-Glutamyltranspeptidase (GGT) is overexpressed in several types of cancer. Existing GGT-targeting fluorescence probes can image these cancers, but the fluorescent hydrolysis product leaks from the target cancer cells during prolonged incubation or fixation. Here, we present a functionalized fluorescence probe for GGT, 4-CH F-HMDiEtR-gGlu, which is designed to generate an azaquinone methide intermediate during activation by GGT; this intermediate reacts with intracellular nucleophiles to generate a fluorescent adduct that is trapped inside the cells, without loss of the target enzyme activity. Application of the probe to patient-derived xenograft (PDX) mice enabled in vivo cancer imaging for a prolonged period and was also compatible with fixation and immunostaining of the cancer tissue.
γ-谷氨酰转肽酶(GGT)在多种类型的癌症中过度表达。现有的 GGT 靶向荧光探针可对这些癌症进行成像,但在长时间孵育或固定过程中,荧光水解产物会从靶癌细胞中泄漏。在这里,我们提出了一种用于 GGT 的功能化荧光探针,4-CH F-HMDiEtR-gGlu,其设计目的是在 GGT 激活过程中产生氮杂醌甲亚胺中间体;该中间体与细胞内亲核试剂反应,生成一种被捕获在细胞内的荧光加合物,而不会损失靶酶活性。该探针在患者来源的异种移植(PDX)小鼠中的应用使体内癌症成像能够持续较长时间,并且还与癌症组织的固定和免疫染色兼容。