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NEAR INFRARED FLUOROGEN AND FLUORESCENT ACTIVATING PROTEINS FOR IN VIVO IMAGING AND LIVE-CELL BIOSENSING

机译:用于体内成像和活细胞生物传感的近红外荧光素和荧光激活蛋白

摘要

Tissue slices and whole organisms offer substantial challenges to fluorescence imaging. Autofluorescence and absorption via intrinsic chromophores, such as flavins, melanin, and hemoglobins, confound and degrade output from all fluorescent tags. An “optical window,” farther red than most autofluorescence sources and in a region of low hemoglobin and water absorbance, lies between 650 and 900 nm. This valley of relative optical clarity is an attractive target for fluorescence-based studies within tissues, intact organs, and living organisms. Novel fluorescent tags were developed herein, based upon a genetically targeted fluorogen activating protein and cognate fluorogenic dye that yields emission with a peak at 733 nm exclusively when complexed as a “fluoromodule”. This tool improves substantially over previously described far-red/NIR fluorescent proteins in terms of brightness, wavelength, and flexibility by leveraging the flexibility of synthetic chemistry to produce novel chromophores.
机译:组织切片和整个生物体对荧光成像提出了重大挑战。通过固有的生色团(例如黄素,黑色素和血红蛋白)的自发荧光和吸收会混淆并降低所有荧光标签的输出。 “光学窗口”比大多数自发荧光源更红,并且在血红蛋白和吸水率低的区域内,位于650至900 nm之间。相对光学清晰度的低谷是组织,完整器官和活生物体内基于荧光的研究的一个有吸引力的目标。本文基于遗传靶向的氟活化蛋白和同源荧光染料开发了新颖的荧光标签,所述荧光染料在与“氟模块”复合时仅在733 nm处产生峰值发射。通过利用合成化学的灵活性来产生新型生色团,该工具在亮度,波长和灵活性方面大大优于先前描述的远红/ NIR荧光蛋白。

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