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单分子多分析物(Ca2+、Mg2+)荧光探针及其在生物成像中的应用。

Single molecular multianalyte (Ca2+, Mg2+) fluorescent probe and applications to bioimaging.

作者信息

Komatsu Hirokazu, Miki Takahiro, Citterio Daniel, Kubota Takeshi, Shindo Yutaka, Kitamura Yoshiichiro, Oka Kotaro, Suzuki Koji

机构信息

Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan.

出版信息

J Am Chem Soc. 2005 Aug 10;127(31):10798-9. doi: 10.1021/ja0528228.

Abstract

Intracellular signal transduction relies on spatial and temporal signal transmitter dynamics. To clarify the correlations of these transmitter molecules, multicolor-imaging has been widely used. However, in the case of applying multiple indicators in a cell, spectral overlap of the indicators prevents accurate quantitative analysis. Moreover, the invasive (toxic) effect, the localization, the metabolism, as well as photobleaching of these indicators complicate the situation. Here, we show that single-molecular multifluorescent probes can overcome these problems. While intracellular calcium plays a critical role as a signal transmitter and magnesium acts as a cofactor in many situations, the correlations between the two cations are now the main issue. We designed and synthesized a Ca2+-Mg2+ responsive multifluorescent probe, KCM-1. KCM-1 shows a spectral blue shift upon complexation to Ca2+ and a red shift to the presence of Mg2+. With data analyzed at different excitation wavelengths, the concentrations of Ca2+ and Mg2+ are simultaneously quantified. Furthermore, by using the AM-ester method, intracellular Ca2+ and Mg2+ concentrations are simultaneously imaged. Such a type of intracellular multiple analyte imaging by a single-molecular multifluorescent probe is successfully demonstrated for the first time.

摘要

细胞内信号转导依赖于空间和时间上的信号转导分子动力学。为了阐明这些转导分子之间的相关性,多色成像已被广泛应用。然而,在细胞中应用多种指示剂的情况下,指示剂的光谱重叠会妨碍准确的定量分析。此外,这些指示剂的侵入性(毒性)效应、定位、代谢以及光漂白使情况变得复杂。在此,我们表明单分子多荧光探针可以克服这些问题。虽然细胞内钙作为信号转导分子起着关键作用,并且镁在许多情况下作为辅助因子起作用,但这两种阳离子之间的相关性现在是主要问题。我们设计并合成了一种Ca2+-Mg2+响应性多荧光探针KCM-1。KCM-1与Ca2+络合时显示光谱蓝移,与Mg2+存在时显示红移。通过在不同激发波长下分析数据,可同时定量Ca2+和Mg2+的浓度。此外,通过使用AM酯法,可同时对细胞内Ca2+和Mg2+浓度进行成像。首次成功证明了通过单分子多荧光探针进行这种类型的细胞内多分析物成像。

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