Krissanaprasit Abhichart, Key Carson M, Pontula Sahil, LaBean Thomas H
Department of Materials Science and Engineering, College of Engineering, North Carolina State University, Raleigh, North Carolina 27695, United States.
Department of Biomedical Engineering, Duke University, Durham, North Carolina 27708, United States.
Chem Rev. 2021 Nov 24;121(22):13797-13868. doi: 10.1021/acs.chemrev.0c01332. Epub 2021 Jun 22.
Researchers have worked for many decades to master the rules of biomolecular design that would allow artificial biopolymer complexes to self-assemble and function similarly to the diverse biochemical constructs displayed in natural biological systems. The rules of nucleic acid assembly (dominated by Watson-Crick base-pairing) have been less difficult to understand and manipulate than the more complicated rules of protein folding. Therefore, nucleic acid nanotechnology has advanced more quickly than protein design, and recent years have seen amazing progress in DNA and RNA design. By combining structural motifs with aptamers that act as affinity handles and add powerful molecular recognition capabilities, nucleic acid-based self-assemblies represent a diverse toolbox for use by bioengineers to create molecules with potentially revolutionary biological activities. In this review, we focus on the development of self-assembling nucleic acid nanostructures that are functionalized with nucleic acid aptamers and their great potential in wide ranging application areas.
几十年来,研究人员一直致力于掌握生物分子设计的规则,以使人工生物聚合物复合物能够自我组装,并发挥与天然生物系统中展示的各种生化结构类似的功能。与更为复杂的蛋白质折叠规则相比,核酸组装规则(以沃森-克里克碱基配对为主)更容易理解和操控。因此,核酸纳米技术的发展比蛋白质设计更快,近年来在DNA和RNA设计方面取得了惊人的进展。通过将结构基序与充当亲和手柄并增添强大分子识别能力的适体相结合,基于核酸的自组装体为生物工程师提供了一个多样化的工具箱,用于创造具有潜在革命性生物活性的分子。在本综述中,我们重点关注用核酸适体功能化的自组装核酸纳米结构的发展及其在广泛应用领域的巨大潜力。