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用于细胞内镉成像的双光子荧光探针。

Two-photon fluorescent probe for cadmium imaging in cells.

机构信息

Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, P. R. China.

出版信息

Analyst. 2012 Apr 21;137(8):1837-45. doi: 10.1039/c2an16254g. Epub 2012 Mar 5.

Abstract

A novel two-photon excited fluorescent probe for cadmium (named as TPCd) was designed and synthesized utilizing a prodan (6-acetyl-2-methoxynaphthalene) derivative as the two-photon fluorophore and an o-phenylenediamine derivative as the Cd(2+) chelator, which possessed favorable photophysical properties and good water-solubility. The probe was designed with a photoinduced electron transfer (PET) mechanism and thus was weakly fluorescent itself. After binding with Cd(2+) which blocked the PET process, the fluorescence intensity of the probe was enhanced by up to 15-fold under one-photon excitation (OPE) and 27-fold under two-photon excitation (TPE), respectively. The two-photon action cross-section (Φδ) of the TPCd-Cd complex at 740 nm reached 109 GM compared to 3.6 GM for free TPCd, indicating the promising prospect of the probe in two-photon application. TPCd chelated Cd(2+) with 1 : 1 stoichiometry, and the apparent dissociation constant (K(d)) was 6.1 × 10(-5) M for the one-photon mode and 7.2 × 10(-5) M for the two-photon mode. The probe responded to Cd(2+) over a wide linear range from 0.1 to 30 μM with a detection limit of 0.04 μM. High selectivity of the probe towards Cd(2+) was acquired in Tris-HCl/sodium phosphate buffer. The probe was pH-independent in the biologically relevant pH range and non-toxic to living cells at reasonable concentration levels, warranting its in vivo applications. Through two-photon microscopy imaging, the probe was successfully applied to detect Cd(2+) uptake in living HepG2 cells.

摘要

一种新型的双光子激发荧光探针用于镉(命名为 TPCd),利用一个 prodan(6-乙酰-2-甲氧基萘)衍生物作为双光子荧光团和邻苯二胺衍生物作为 Cd(2+)螯合剂,具有良好的光物理性质和良好的水溶性。该探针采用光诱导电子转移(PET)机制设计,因此本身荧光较弱。与 Cd(2+)结合后,阻断了 PET 过程,探针在单光子激发(OPE)下的荧光强度增强了 15 倍,在双光子激发(TPE)下增强了 27 倍。TPCd-Cd 配合物在 740nm 处的双光子作用截面(Φδ)达到 109 GM,而游离 TPCd 的Φδ为 3.6 GM,表明该探针在双光子应用方面有很大的应用前景。TPCd 与 Cd(2+)以 1:1 的化学计量比螯合,单光子模式下的表观解离常数(K(d))为 6.1×10(-5)M,双光子模式下为 7.2×10(-5)M。该探针对 Cd(2+)的线性响应范围从 0.1 到 30μM,检测限为 0.04μM。该探针对 Cd(2+)具有较高的选择性,在 Tris-HCl/磷酸钠缓冲液中。该探针在生物相关 pH 范围内 pH 独立,在合理浓度水平下对活细胞无毒,保证了其在体内的应用。通过双光子显微镜成像,该探针成功应用于检测活 HepG2 细胞中 Cd(2+)的摄取。

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