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DNA 自组装在细胞表面驱动膜蛋白的单向聚类,从而调节细胞行为。

DNA Self-Assembly on the Cell Surface Drives Unidirectional Clustering of Membrane Proteins for the Modulation of Cell Behaviors.

机构信息

Institute of Molecular Medicine, Department of Laboratory Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, State Key Laboratory of Oncogene and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China.

出版信息

Nano Lett. 2022 Apr 27;22(8):3410-3416. doi: 10.1021/acs.nanolett.2c00680. Epub 2022 Apr 7.

Abstract

Cell membrane proteins play a pivotal role in regulating intracellular signal transductions and cell behaviors. Many membrane proteins form clusters in order to initiate downstream signaling pathways for the modulation of cell behaviors. Developing rational methods to program the clustering of designated membrane proteins on the cell surface to form large assemblies remains challenging. Here we use the membrane-anchored DNA hybridization chain reaction (HCR) to induce DNA self-assembly on the live cell surface and drive the unidirectional clustering of membrane proteins for the modulation of cell behaviors. Reactive DNA strands are specifically anchored onto the membrane proteins of interest by using DNA aptamers. Upon activation, the chain reaction between the protein-anchored DNA strands drives the assembly of membrane proteins forming one-dimensional clusters. We demonstrate both homogeneous and heterogeneous clustering of membrane proteins on multiple cell types that exhibit a potent capability for modulating cell behaviors including migration, proliferation, and survival.

摘要

细胞膜蛋白在调节细胞内信号转导和细胞行为方面起着关键作用。许多膜蛋白形成簇,以便启动下游信号通路,从而调节细胞行为。开发合理的方法来编程指定的膜蛋白在细胞表面上的聚类以形成大的组装仍然具有挑战性。在这里,我们使用膜锚定 DNA 杂交链式反应(HCR)在活细胞表面诱导 DNA 自组装,并驱动膜蛋白的单向聚类以调节细胞行为。通过使用 DNA 适体,将反应性 DNA 链特异性地锚定到感兴趣的膜蛋白上。在激活后,蛋白锚定 DNA 链之间的链式反应驱动膜蛋白的组装形成一维簇。我们展示了多种细胞类型上的膜蛋白的同质和异质聚类,这些聚类表现出调节细胞行为的强大能力,包括迁移、增殖和存活。

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