School of Chemistry and Environment, Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine, South China Normal University, Guangzhou, Guangdong, 510006, People's Republic of China.
, No. 378 Waihuan West Road, University City, Guangzhou, Guangdong, 510006, China.
J Fluoresc. 2017 Jul;27(4):1495-1503. doi: 10.1007/s10895-017-2089-z. Epub 2017 May 15.
Indole propionic acid (IPA) is one of the important plant growth hormones for promoting rooting and fruiting. Labeling IPA receptor in plant tissues is able to further track the signal transduction processes of IPA and uncover the function mechanism of IPA on crop productions. In this paper, a tunable and nontoxic fluorescent probe for IPA receptors was designed and synthetized base on carbon dots (C dots). Firstly carboxyl-modified carbon dots were prepared by high temperature cracking of citric acid. The fluorescence emission wavelengths of C dots varied with the excitation wavelengths change. Then IPA-modified carbon dots (IPA-C dots) were prepared by coupling the amino of tryptophan with the carboxyl of as-prepared carbon dots. Compared with C dots, the fluorescence intensity of IPA-C dots was double and the fluorescence stability was satisfactory under various conditions. This probe retained the biological activity of IPA and acted as target recognition of IPA receptors in plant tissues. The probe could avoid green fluorescence background of plants. The imaging results showed that the IPA receptors mainly existed on the membrane of stele. The toxicity test indicated the probe was less toxic than traditional inorganic semiconductor quantum dots.
吲哚丙酸(IPA)是促进生根和结果的重要植物生长激素之一。对植物组织中的 IPA 受体进行标记,能够进一步跟踪 IPA 的信号转导过程,揭示 IPA 对作物产量的作用机制。本文基于碳点(C 点)设计并合成了一种可调谐且无毒的 IPA 受体荧光探针。首先,通过柠檬酸的高温裂解脱羧基得到羧基化的碳点。碳点的荧光发射波长随激发波长的变化而变化。然后,通过将色氨酸的氨基与制备的碳点的羧基偶联,制备 IPA 修饰的碳点(IPA-C 点)。与 C 点相比,IPA-C 点的荧光强度增加了一倍,在各种条件下的荧光稳定性都令人满意。该探针保留了 IPA 的生物活性,并在植物组织中作为 IPA 受体的靶标识别。探针可以避免植物的绿色荧光背景。成像结果表明,IPA 受体主要存在于中柱的膜上。毒性试验表明,该探针的毒性比传统的无机半导体量子点低。