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Luciferase and Luciferin Co-immobilized Mesoporous Silica Nanoparticle Materials for Intracellular Biocatalysis

机译:萤光素酶和萤光素共固定介孔二氧化硅纳米粒子材料的细胞内生物催化

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摘要

We report a gold nanoparticle (AuNP)-capped mesoporous silica nanoparticle (Au-MSN) platform for intracellular codelivery of an enzyme and a substrate with retention of bioactivity. As a proof-of-concept demonstration, Au-MSNs are shown to release luciferin from the interior pores of MSN upon AuNP uncapping in response to disulfide-reducing antioxidants and codeliver bioactive luciferase from the PEGylated exterior surface of Au-MSN to Hela cells. The effectiveness of luciferase-catalyzed luciferin oxidation and luminescence emission in the presence of intracellular ATP was measured by a luminometer. Overall, the chemical tailorability of the Au-MSN platform to retain enzyme bioactivity, the ability to codeliver enzyme and substrate, and the potential for imaging tumor growth and metastasis afforded by intracellular ATP- and glutathione-dependent bioluminescence make this platform appealing for intracellular controlled catalysis and tumor imaging.
机译:我们报告了金纳米粒子(AuNP)封顶的介孔二氧化硅纳米粒子(Au-MSN)平台的酶和基质的生物活性保留的细胞内代码传递。作为概念验证的证据,Au-MSN被显示为在对AuNP开盖后从MSN的内部孔中释放萤光素,以响应于还原二硫键的抗氧化剂,并从Au-MSN的PEG化外表面向Hela细胞提供生物活性荧光素酶。通过发光计测量在细胞内ATP存在下荧光素酶催化的荧光素的氧化和发光发射的有效性。总体而言,Au-MSN平台保留酶生物活性的化学适应性,编码酶和底物的能力以及细胞内ATP和谷胱甘肽依赖性生物发光提供的肿瘤生长和转移成像的潜力使该平台吸引细胞内控制催化和肿瘤成像。

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