DNA折纸
内吞作用
纳米技术
内化
DNA
DNA纳米技术
内吞循环
纳米结构
生物物理学
材料科学
生物系统
细胞
生物
化学
生物化学
作者
Anjali Rajwar,Shravani Reddy Shetty,Payal Vaswani,Vinod Morya,Amlan Barai,Shamik Sen,Mahendra Sonawane,Dhiraj Bhatia
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-06-17
卷期号:16 (7): 10496-10508
被引量:69
标识
DOI:10.1021/acsnano.2c01382
摘要
Fabrication of nanoscale DNA devices to generate 3D nano-objects with precise control of shape, size, and presentation of ligands has shown tremendous potential for therapeutic applications. The interactions between the cell membrane and different topologies of 3D DNA nanostructures are crucial for designing efficient tools for interfacing DNA devices with biological systems. The practical applications of these DNA nanocages are still limited in cellular and biological systems owing to the limited understanding of their interaction with the cell membrane and endocytic pathway. The correlation between the geometry of DNA nanostructures and their internalization efficiency remains elusive. We investigated the influence of the shape and size of 3D DNA nanostructures on their cellular internalization efficiency. We found that one particular geometry, i.e., the tetrahedral shape, is more favored over other designed geometries for their cellular uptake in 2D and 3D cell models. This is also replicable for cellular processes like cell invasion assays in a 3D spheroid model, and passing the epithelial barriers in in vivo zebrafish model systems. Our work provides detailed information for the rational design of DNA nanodevices for their upcoming biological and biomedical applications.
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