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载酶纳米磷酸钙用于原位乳腺癌的持续生物发光成像

Luciferase-Loaded Calcium Phosphate Nanoparticles for Persistent Bioluminescence Imaging of Orthotopic Breast Tumors.

机构信息

Department of Neurosurgery, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230031, China.

Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, China.

出版信息

Anal Chem. 2024 Sep 10;96(36):14320-14325. doi: 10.1021/acs.analchem.4c02289. Epub 2024 Aug 29.

Abstract

Bioluminescence imaging (BLI) is an important noninvasive optical imaging technique that has been widely used to monitor many biological processes due to its high sensitivity, resolution, and signal-to-noise ratio. However, the BLI technique based on the firefly luciferin-luciferase system is limited by the expression of exogenous luciferase and the short half-life of firefly luciferin, which pose challenges for long-term tracking in vivo. To solve the problems, here we rationally designed an intelligent strategy for persistent BLI in tumors by combining luciferase-loaded calcium phosphate nanoparticles (Luc@CaP NPs) to provide luciferase and the probe Cys(SEt)-Lys-CBT (CKCBT) to slowly produce the luciferase substrate amino luciferin (Am-luciferin). Luc@CaP NPs constructed with CaP as a carrier could enable luciferase activity to be maintained in vivo for at least 12 h. And compared to the conventional substrate luciferin, CKCBT apparently prolonged the BL time by up to 2 h through GSH-induced intracellular self-assembly and subsequent protease degradation-induced release of Am-luciferin. We anticipate that this strategy could be applied for clinical translation in more disease diagnosis and treatment in the near future.

摘要

生物发光成像是一种重要的非侵入性光学成像技术,由于其具有高灵敏度、高分辨率和高信噪比等优点,已被广泛应用于监测多种生物过程。然而,基于萤火虫荧光素酶系统的 BLI 技术受到外源荧光酶表达和萤火虫荧光素半衰期短的限制,这给体内长期跟踪带来了挑战。为了解决这些问题,我们通过将负载荧光酶的磷酸钙纳米颗粒 (Luc@CaP NPs) 与探针 Cys(SEt)-Lys-CBT (CKCBT) 结合,设计了一种在肿瘤中进行持续生物发光成像的智能策略,以提供荧光酶和缓慢产生荧光酶底物氨基荧光素 (Am-luciferin)。以 CaP 为载体构建的 Luc@CaP NPs 能够使荧光酶活性在体内至少维持 12 小时。与传统的底物荧光素相比,CKCBT 通过 GSH 诱导的细胞内自组装以及随后的蛋白酶降解诱导的 Am-luciferin 释放,明显延长了 BL 时间,长达 2 小时。我们预计,在不久的将来,该策略将能够应用于更多疾病的诊断和治疗的临床转化。

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