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基于 DNA 纳米支架模板化多价双特异性适体的靶向细胞-细胞相互作用。

Targeted cell-cell interactions by DNA nanoscaffold-templated multivalent bispecific aptamers.

机构信息

Center of Single Molecule Biophysics, The Biodesign Institute, Arizona State University, Tempe, Arizona 85287, USA.

出版信息

Small. 2011 Jun 20;7(12):1673-82. doi: 10.1002/smll.201002292. Epub 2011 May 2.

Abstract

Cell-cell interactions are essential for multicellular organisms, playing important roles in their development, function, and immunity. Herein a bottom-up strategy to construct self-assembled DNA nanostructures is reported, consisting of multivalent, bispecific, cell-targeting aptamers to specifically induce cell-cell interactions. Various DNA nanoscaffolds are rationally designed to assemble aptamers with different valencies and flexibilities, and their cellular binding capabilities are tested. Multivalent aptamers, assembled on more rigid scaffolds, display higher binding activities. Further, multivalent bispecific aptamer fusion molecules are constructed based on this configuration, and successfully link two types of cells. Using cell-targeting aptamers, the presented strategy eliminates the need to chemically modify cell surfaces and offers excellent cell specificity, binding efficiency, and stability. This proof-of-concept study establishes that multivalent bispecific aptamers linked on DNA-nanoscaffolds can mediate cellular engagement, which could lead to their use in directing or guiding cell-cell interactions in many biological events.

摘要

细胞间相互作用对于多细胞生物至关重要,在其发育、功能和免疫中发挥着重要作用。在此,我们报告了一种自下而上的策略来构建自组装 DNA 纳米结构,该结构由多价、双特异性、细胞靶向适体组成,可特异性诱导细胞间相互作用。合理设计了各种 DNA 纳米支架来组装具有不同价数和柔韧性的适体,并测试了它们的细胞结合能力。在更刚性的支架上组装的多价适体显示出更高的结合活性。此外,还基于这种结构构建了多价双特异性适体融合分子,并成功连接了两种类型的细胞。使用细胞靶向适体,该策略不需要对细胞表面进行化学修饰,具有优异的细胞特异性、结合效率和稳定性。这项概念验证研究表明,连接在 DNA 纳米支架上的多价双特异性适体可以介导细胞结合,这可能导致它们在许多生物事件中用于指导或引导细胞间相互作用。

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