Department of Chemistry, University of Massachusetts Amherst, Amherst, MA, 01003, USA.
Molecular and Cellular Biology Program, University of Massachusetts Amherst, Amherst, USA.
Angew Chem Int Ed Engl. 2020 Jun 22;59(26):10456-10460. doi: 10.1002/anie.202002748. Epub 2020 Apr 15.
The development of nanoparticle-based biomedical applications has been hampered due to undesired off-target effects. Herein, we outline a cellular AND gate to enhance uptake selectivity, in which a nanoassembly-cell interaction is turned on, only in the concurrent presence of two different protein functions, an enzymatic reaction (alkaline phosphatase, ALP) and a ligand-protein (carbonic anhydrase IX, CA IX) binding event. Selective uptake of nanoassemblies was observed in cells that overexpress both of these proteins (unicellular AND gate). Interestingly, selective uptake can also be achieved in CA IX overexpressed cells, when cocultured with ALP overexpressed cells, where the nanoassembly presumably acts as a mediator for cell-cell communication (bicellular AND gate). This logic-gated cellular uptake could find use in applications such as tumor imaging or theranostics.
基于纳米粒子的生物医学应用的发展受到了阻碍,因为存在不理想的脱靶效应。在此,我们概述了一个细胞“与”门,以增强摄取选择性,其中纳米组装体-细胞相互作用仅在两种不同的蛋白质功能(酶反应(碱性磷酸酶,ALP)和配体-蛋白质(碳酸酐酶 IX,CA IX)结合事件)同时存在时才开启。在过表达这两种蛋白质的细胞中观察到纳米组装体的选择性摄取(单细胞“与”门)。有趣的是,当与过表达 ALP 的细胞共培养时,在过表达 CA IX 的细胞中也可以实现选择性摄取,其中纳米组装体可能充当细胞-细胞通讯的介质(双细胞“与”门)。这种基于逻辑门的细胞摄取可用于肿瘤成像或治疗等应用。