PrismaLuc luciferase enables tunable near-infrared bioluminescence for in vivo imaging.

IF 3.9 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Felipe Gama-Franceschi, Rachel Friedman Ohana, Chao Gao, Thomas Kirkland, Laura Mezzanotte
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引用次数: 0

Abstract

Bioluminescence imaging (BLI) enables non-invasive monitoring of biological processes in living animals, yet most bioluminescent reporters emit at fixed wavelengths with limited spectral flexibility, constraining their use in multiplexed and deep-tissue applications. Bioluminescence resonance energy transfer (BRET) offers a solution by coupling a luciferase to a proximal fluorescent protein or synthetic fluorophore that absorbs the emitted light and re-emits it at a longer wavelength. However, existing BRET systems built from luciferase-fluorescent protein fusions are limited by suboptimal energy transfer efficiency and the fixed photophysical properties of their genetically encoded chromophores. We recently introduced PrismaLuc, a high-efficiency BRET reporter, in which a circularly permuted NanoLuc is inserted into HaloTag, enabling efficient energy transfer to a covalently bound synthetic fluorophore whose emission wavelength is selected by choice of ligand. In our initial report, PrismaLuc was paired with JF549 HaloTag ligand for two-colour cell-based assays. Here, we extend PrismaLuc to in vivo bioluminescence imaging using far-red and near-infrared HaloTag ligands. In cultured cells, labelling with JF608 and JF669 HaloTag ligands produced emission peaks at 640 and 690 nm, respectively. Direct comparison with established BRET reporters revealed greater photon output at wavelengths above 665 nm, which are less attenuated in tissue. In tumour-bearing mice, PrismaLuc:JF669 produced an emission peak of approximately 700 nm, and in vivo fluorescence imaging confirmed sufficient JF669 HaloTag ligand bioavailability to label PrismaLuc expressed in xenograft tumours. Finally, dual-colour imaging in mice co-implanted with NanoLuc- and PrismaLuc-expressing cells demonstrated clear spectral separation, enabling multiplexed detection within the same animal. Together, these results establish PrismaLuc as a tunable platform for near-infrared and dual-colour bioluminescence imaging in vivo.

PrismaLuc荧光素酶可调近红外生物发光在体内成像。
生物发光成像(BLI)能够对活体动物的生物过程进行无创监测,但大多数生物发光报告器在固定波长发射,光谱灵活性有限,限制了它们在多路复用和深层组织应用中的应用。生物发光共振能量转移(BRET)提供了一种解决方案,通过将荧光素酶偶联到近端荧光蛋白或合成荧光团,吸收发射的光并以更长的波长重新发射。然而,现有的由荧光素酶-荧光蛋白融合构建的BRET系统受到能量转移效率不理想和其遗传编码发色团固定的光物理特性的限制。我们最近推出了PrismaLuc,一种高效的BRET报告器,其中一个循环排列的NanoLuc插入到HaloTag中,能够有效地将能量转移到共价结合的合成荧光团,其发射波长可通过选择配体来选择。在我们最初的报告中,PrismaLuc与JF549 HaloTag配体配对,用于双色细胞检测。在这里,我们将PrismaLuc扩展到使用远红和近红外HaloTag配体的体内生物发光成像。在培养细胞中,JF608和JF669 HaloTag配体标记分别在640和690 nm处产生发射峰。与已建立的BRET报告器的直接比较显示,在665 nm以上的波长处光子输出更大,在组织中衰减较小。在携带肿瘤的小鼠中,PrismaLuc:JF669产生约700 nm的发射峰,体内荧光成像证实JF669 HaloTag配体的生物利用度足以标记PrismaLuc在异种移植肿瘤中的表达。最后,在同时植入NanoLuc和prismaluc表达细胞的小鼠中,双色成像显示出清晰的光谱分离,可以在同一动物中进行多路检测。总之,这些结果确立了PrismaLuc作为近红外和双色生物发光在体内成像的可调平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.10
自引率
0.00%
发文量
128
审稿时长
10 weeks
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