首页> 外文期刊>Journal of the American Chemical Society >Remarkable Enhancement of Chemiluminescent Signal by Dioxetane-Fluorophore Conjugates: Turn-ON Chemiluminescence Probes with Color Modulation for Sensing and Imaging
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Remarkable Enhancement of Chemiluminescent Signal by Dioxetane-Fluorophore Conjugates: Turn-ON Chemiluminescence Probes with Color Modulation for Sensing and Imaging

机译:二氧杂环丁烷-荧光团的化学发光信号显着增强:具有感测和成像颜色调制功能的开启化学发光探针。

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摘要

Chemiluminescence is among the most sensitive methods for achieving a high signal-to-noise ratio in various chemical and biological applications. We have developed a modular practical synthetic route for preparation of turn-ON fluorophore-tethered dioxetane chemiluminescent probes. The chemiluminescent emission of the probes was significantly amplified through an energy-transfer mechanism under physiological conditions. Two probes were composed with green and near-infrared (NIR) fluorescent dyes tethered to Schaap's dioxetane. While both probes were able to provide chemiluminescence in vivo images following subcutaneous injection, only the NIR probe could provide a chemiluminescence image following intraperitoneal injection. These are the first in vivo images produced by Schaap's dioxetane chemiluminescence probes with no need of an enhancer. Previously, chemiluminescence cell images could only be obtained with a luciferin-based probe. Our NIR probe was able to image cells transfected with β-galactosidase gene by chemiluminescence microscopy. We also report, for the first time, the instability of dioxetane-fluorophore conjugates to ambient light. Our synthetic route effectively overcomes this limitation through a late-stage functionalization of the dioxetane intermediate. We anticipate that our practical synthetic methodology will be useful for preparation of various chemiluminescent probes for numerous applications.
机译:化学发光是在各种化学和生物学应用中实现高信噪比的最敏感方法之一。我们已经开发出一种模块化的实用合成路线,用于制备开启荧光团的二氧杂环丁烷化学发光探针。探针的化学发光通过生理条件下的能量转移机制被显着放大。两个探针由束缚在Schaap二氧杂环丁烷上的绿色和近红外(NIR)荧光染料组成。尽管两种探针都能在皮下注射后提供体内化学发光图像,但只有NIR探针可以在腹膜内注射后提供化学发光图像。这些是Schaap的二氧杂环丁烷化学发光探针无需增强剂产生的第一批体内图像。以前,化学发光细胞图像只能使用基于荧光素的探针获得。我们的NIR探针能够通过化学发光显微镜对转染了β-半乳糖苷酶基因的细胞进行成像。我们还首次报告了二氧杂环丁烷-荧光团偶联物对环境光的不稳定性。我们的合成路线通过二氧杂环丁烷中间体的后期功能化有效地克服了这一限制。我们预计,我们实用的合成方法将可用于制备多种用途的各种化学发光探针。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2016年第40期|13438-13446|共9页
  • 作者单位

    School of Chemistry, Raymond and Beverly Sadder Faculty of Exact Sciences, Sackler School of Medidne, Tel Aviv University, Tel Aviv 69978, Israel;

    Department of Physiology and Pharmacology, Sackler School of Medidne, Tel Aviv University, Tel Aviv 69978, Israel;

    Bioimaging Center, University of Geneva, CH-1211 Geneva, Switzerland;

    Department of Physiology and Pharmacology, Sackler School of Medidne, Tel Aviv University, Tel Aviv 69978, Israel;

    School of Chemistry, Raymond and Beverly Sadder Faculty of Exact Sciences, Sackler School of Medidne, Tel Aviv University, Tel Aviv 69978, Israel;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 03:08:58

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