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通过发光的非束缚激发实现荧光的体外和体内演示(FUEL)。

In vitro and in vivo demonstrations of Fluorescence by Unbound Excitation from Luminescence (FUEL).

作者信息

Dragavon Joe, Rekiki Abdessalem, Theodorou Ioanna, Samson Chelsea, Blazquez Samantha, Rogers Kelly L, Tournebize Régis, Shorte Spencer

机构信息

Plate-Forme d'Imagerie Dynamique, Imagopole, Institut Pasteur, Paris, France.

出版信息

Methods Mol Biol. 2014;1098:259-70. doi: 10.1007/978-1-62703-718-1_20.

Abstract

Bioluminescence imaging is a powerful technique that allows for deep-tissue analysis in living, intact organisms. However, in vivo optical imaging is compounded by difficulties due to light scattering and absorption. While light scattering is relatively difficult to overcome and compensate, light absorption by biological tissue is strongly dependent upon wavelength. For example, light absorption by mammalian tissue is highest in the blue-yellow part of the visible energy spectrum. Many natural bioluminescent molecules emit photonic energy in this range, thus in vivo optical detection of these molecules is primarily limited by absorption. This has driven efforts for probe development aimed to enhance photonic emission of red light that is absorbed much less by mammalian tissue using either direct genetic manipulation, and/or resonance energy transfer methods. Here we describe a recently identified alternative approach termed Fluorescence by Unbound Excitation from Luminescence (FUEL), where bioluminescent molecules are able to induce a fluorescent response from fluorescent nanoparticles through an epifluorescence mechanism, thereby significantly increasing both the total number of detectable photons as well as the number of red photons produced.

摘要

生物发光成像是一种强大的技术,可对完整的活体生物进行深层组织分析。然而,由于光散射和吸收,体内光学成像面临诸多困难。虽然光散射相对难以克服和补偿,但生物组织对光的吸收强烈依赖于波长。例如,哺乳动物组织在可见能谱的蓝黄色部分对光的吸收最高。许多天然生物发光分子在这个范围内发射光子能量,因此这些分子的体内光学检测主要受吸收限制。这推动了旨在通过直接基因操作和/或共振能量转移方法增强哺乳动物组织吸收少得多的红光光子发射的探针开发工作。在此,我们描述一种最近发现的称为“发光非束缚激发荧光(FUEL)”的替代方法,即生物发光分子能够通过落射荧光机制诱导荧光纳米颗粒产生荧光响应,从而显著增加可检测光子的总数以及产生的红光光子数量。

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