Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, The Netherlands.
School of Biochemistry, University of Bristol, Bristol, UK.
Methods Mol Biol. 2024;2800:35-53. doi: 10.1007/978-1-0716-3834-7_4.
Clustering of type II tumor necrosis factor (TNF) receptors (TNFRs) is essential for their activation, yet currently available drugs fail to activate signaling. Some strategies aim to cluster TNFR by using multivalent streptavidin or scaffolds based on dextran or graphene. However, these strategies do not allow for control of the valency or spatial organization of the ligands, and consequently control of the TNFR activation is not optimal. DNA origami nanostructures allow nanometer-precise control of the spatial organization of molecules and complexes, with defined spacing, number and valency. Here, we demonstrate the design and characterization of a DNA origami nanostructure that can be decorated with engineered single-chain TNF-related apoptosis-inducing ligand (SC-TRAIL) complexes, which show increased cell killing compared to SC-TRAIL alone on Jurkat cells. The information in this chapter can be used as a basis to decorate DNA origami nanostructures with various proteins, complexes, or other biomolecules.
二型肿瘤坏死因子(TNF)受体(TNFR)的聚类对于其激活至关重要,但目前可用的药物无法激活信号。一些策略旨在通过使用多价链霉亲和素或基于葡聚糖或石墨烯的支架来聚类 TNFR。然而,这些策略不允许控制配体的价数或空间组织,因此对 TNFR 激活的控制并不理想。DNA 折纸纳米结构允许分子和复合物的空间组织以纳米级精度进行控制,具有确定的间隔、数量和价数。在这里,我们展示了一种 DNA 折纸纳米结构的设计和表征,该结构可以用工程化的单链 TNF 相关凋亡诱导配体(SC-TRAIL)复合物进行修饰,与单独使用 SC-TRAIL 相比,该复合物在 Jurkat 细胞上显示出更强的细胞杀伤作用。本章中的信息可用于用各种蛋白质、复合物或其他生物分子来修饰 DNA 折纸纳米结构。