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基于硫化银量子点的自发光近红外二区生物发光成像探针。

Self-illuminating NIR-II bioluminescence imaging probe based on silver sulfide quantum dots.

机构信息

Key Laboratory of Radiation Medicine and Protection, School for Radiological and Interdisciplinary Sciences (RAD-X), Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Soochow University, Suzhou 215123, P. R. China.

出版信息

ACS Nano. 2022 Oct 25;16(10):16824-16832. doi: 10.1021/acsnano.2c06667. Epub 2022 Sep 30.

DOI:10.1021/acsnano.2c06667
PMID:36178795
Abstract

Bioluminescence (BL) imaging has emerged to tackle the potential challenges of fluorescence (FL) imaging including the autofluorescence background, inhomogeneous illumination over a wide imaging field, and the light-induced overheating effect. Taking advantage of the bioluminescence resonance energy transfer (BRET) mechanism between a conventional luciferin compound and a suitable acceptor, the visible light of the former can be extended to photons with longer wavelengths emitting from the latter. Although BRET-based self-illuminating imaging probes have already been prepared, employing potentially cytotoxic elements as the acceptor with the emission wavelengths which hardly reach the first near-infrared (NIR-I) window, has limited their applications as safe and high performance imaging agents. Herein, we report a biocompatible, self-illuminating, and second near-infrared (NIR-II) emissive probe to address the cytotoxicity concerns as well as improve the penetration depth and spatiotemporal resolution of BL imaging. To this end, NanoLuc luciferase enzyme molecules were immobilized on the surface of silver sulfide quantum dots to oxidize its luciferin substrate and initiate a single-step BRET mechanism, resulting in NIR-II photons from the quantum dots. The resulting dual modality (BL/FL) probes were successfully applied to tumor imaging in mice, demonstrating that NIR-II BL signals could be easily detected from the tumor sites, giving rise to ∼2 times higher signal-to-noise ratios compared to those obtained under FL mode. The results indicated that nontoxic NIR-II emitting nanocrystals deserve more attention to be tailored to fill the growing demands of preparing appropriate agents for high quality BL imaging.

摘要

生物发光 (BL) 成像是为了应对荧光 (FL) 成像的潜在挑战而出现的,包括自发荧光背景、宽成像场的不均匀照明以及光诱导过热效应。利用传统荧光素化合物与合适的受体之间的生物发光共振能量转移 (BRET) 机制,前者的可见光可以扩展到后者发射的波长更长的光子。尽管已经制备了基于 BRET 的自发光成像探针,但由于采用了作为受体的潜在细胞毒性元素,并且其发射波长几乎无法达到第一个近红外 (NIR-I) 窗口,这限制了它们作为安全且高性能的成像剂的应用。在这里,我们报告了一种生物相容性、自发光且发射第二近红外 (NIR-II) 的探针,以解决细胞毒性问题,并提高 BL 成像的穿透深度和时空分辨率。为此,将 NanoLuc 荧光酶分子固定在硫化银量子点的表面上,以氧化其荧光素底物并引发单步 BRET 机制,从而从量子点产生 NIR-II 光子。所得双模 (BL/FL) 探针成功应用于小鼠肿瘤成像,结果表明可以从肿瘤部位轻松检测到 NIR-II BL 信号,与在 FL 模式下获得的信号相比,信噪比提高了约 2 倍。结果表明,无毒的 NIR-II 发射纳米晶体值得更多关注,以满足制备高质量 BL 成像合适试剂的日益增长的需求。

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