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一种源自萘酰亚胺的双光子荧光探针用于活细胞中半胱氨酸的检测与成像。

Two-photon fluorescent probe derived from naphthalimide for cysteine detection and imaging in living cells.

作者信息

Liu Yanbin, Liu Yuwen, Liu Wei, Liang Shucai

机构信息

Institute of Pharmaceutical Analysis, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430072, China.

Department of Chemistry, Wuhan University, Wuhan 430072, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2015 Feb 25;137:509-15. doi: 10.1016/j.saa.2014.08.072. Epub 2014 Sep 2.

Abstract

A maleimide coupling naphthalimide was reported as new two-photon fluorescent (TPF) probe for cysteine (Cys). The probe was weakly fluorescent itself due to the donor-excited photoinduced electron transfer (d-PET). After reaction with Cys, d-PET process was blocked and fluorescence enhancement of the probe was observed at 470 nm. The d-PET principle was rationalized by theoretical calculations with density functional theory and time-dependent density functional theory. Thiol-maleimide addition between the probe and Cys was confirmed by (1)H NMR and mass spectrum measurements. TPF analysis demonstrated a 24.7-fold emission increase of the probe induced by Cys upon excitation at 760 nm. The two-photon action cross-section of probe-Cys adduct at 760 nm reached 42 GM compared to 1.7 GM for free probe. The probe showed high sensitivity and selectivity to Cys over other potential interferences; especially it had the capability to discriminate Cys from glutathione and homocysteine. Through TPF imaging, the probe was successfully applied in the detection of Cys in living cells.

摘要

据报道,一种马来酰亚胺偶联萘酰亚胺是用于检测半胱氨酸(Cys)的新型双光子荧光(TPF)探针。由于供体激发的光诱导电子转移(d-PET),该探针本身荧光较弱。与半胱氨酸反应后,d-PET过程被阻断,在470nm处观察到探针的荧光增强。通过密度泛函理论和含时密度泛函理论的理论计算,对d-PET原理进行了合理化分析。通过核磁共振氢谱(1)H NMR和质谱测量,证实了探针与半胱氨酸之间发生了硫醇-马来酰亚胺加成反应。双光子荧光分析表明,在760nm激发下,半胱氨酸诱导探针的发射增加了24.7倍。与游离探针的1.7GM相比,探针-半胱氨酸加合物在760nm处的双光子作用截面达到42GM。该探针对半胱氨酸具有高灵敏度和选择性,优于其他潜在干扰物;特别是它有能力区分半胱氨酸与谷胱甘肽和同型半胱氨酸。通过双光子荧光成像,该探针成功应用于活细胞中半胱氨酸的检测。

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