Som Madhura, Lal Ratnesh, Ruiz-Velasco Victor
Department of Nanoengineering, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, United States.
Department of Bioengineering, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, United States.
Bioconjug Chem. 2020 Dec 16;31(12):2697-2711. doi: 10.1021/acs.bioconjchem.0c00493. Epub 2020 Nov 24.
Nonmesoporous Janus silica nanobowls (NBs) are unique in that they possess two different nonporous surfaces per particle for loading biological molecules and can thus be designed with multifunctional properties. Although silica NBs have been successfully employed for both targeted therapeutic and diagnostic applications, their ability to deliver DNA has not yet been fully explored. The purpose of this study was to design and develop an in vitro transfection agent that would exploit the distinct characteristics of the silica NB. First, we determined that the NB surface can be linked to either supercoiled cDNA plasmids or vectorless, linear cDNA constructs. Additionally, the linearized cDNA can be functionalized and chemisorbed on NBs to obtain a controlled release. Second, the successful transfection of cells studied was dependent on lipid coating of the NB (LNBs). Although both NBs and LNBs were capable of undergoing endocytosis, NBs appeared to remain within vesicles as shown by transmission electron microscopy (TEM). Third, fluorescence microscopy and Western blotting assays revealed that transfection of four different cell lines and acutely isolated rat sensory neurons with LNBs loaded with either linear or supercoiled cDNA constructs coding for the fluorescent protein, clover and tdTomato, resulted in protein expression. Fourth, two separate opioid receptor-ion channel signaling pathways were functionally reconstituted in HEK cells transfected with LNBs loaded with three separate cDNA constructs. Overall, these results lay the foundation for the use and further development of LNBs as in vitro transfection agents.
非介孔二氧化硅纳米碗(NBs)的独特之处在于,每个颗粒都有两个不同的无孔表面用于负载生物分子,因此可以设计具有多功能特性。尽管二氧化硅NBs已成功用于靶向治疗和诊断应用,但其递送DNA的能力尚未得到充分探索。本研究的目的是设计和开发一种利用二氧化硅NB独特特性的体外转染剂。首先,我们确定NB表面可以与超螺旋cDNA质粒或无载体线性cDNA构建体相连。此外,线性化的cDNA可以被功能化并化学吸附在NBs上以实现控释。其次,所研究细胞的成功转染取决于NB的脂质包被(LNBs)。尽管NBs和LNBs都能够进行内吞作用,但如透射电子显微镜(TEM)所示,NBs似乎保留在囊泡内。第三,荧光显微镜和蛋白质印迹分析表明,用负载有编码荧光蛋白、三叶草和tdTomato的线性或超螺旋cDNA构建体的LNBs转染四种不同的细胞系和急性分离的大鼠感觉神经元,导致了蛋白质表达。第四,在转染了负载有三种不同cDNA构建体的LNBs的HEK细胞中,两种独立的阿片受体-离子通道信号通路在功能上得到了重建。总体而言,这些结果为LNBs作为体外转染剂的使用和进一步开发奠定了基础。