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通过相分离控制的区室化对细胞表面信号进行编程。

Programming cell-surface signaling by phase-separation-controlled compartmentalization.

作者信息

Li Ru, Li Tiantian, Lu Genzhe, Cao Zhi, Chen Bowen, Wang Yalong, Du Juanjuan, Li Pilong

机构信息

Beijing Frontier Research Center for Biological Structure, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, China.

School of Pharmaceutical Sciences, MOE Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology, Tsinghua University, Beijing, China.

出版信息

Nat Chem Biol. 2022 Dec;18(12):1351-1360. doi: 10.1038/s41589-022-01192-3. Epub 2022 Nov 17.

Abstract

The landscape of cell-surface signaling is formidably complex. Robust tools capable of manipulating the spatiotemporal distribution of cell-surface proteins (CSPs) for dissecting signaling are in high demand. Some CSPs are regulated via multivalency-driven liquid-liquid phase separation (LLPS). Employing the robustness and versatility of LLPS, we decided to engineer LLPS-based tools for precisely manipulating CSPs. We generated membrane-tethering LLPS systems by fusing multivalent modular phase-separation scaffold pairs with CSP binders. Phase separation of the scaffold pairs, concomitant compartmentalization of CSPs on membranes, and cluster-dependent signaling outputs of CSPs require membrane recruitment of one or both scaffolds. We also engineered orthogonal phase-separation systems to segregate CSPs into mutually exclusive compartments. The engineered phase-separation systems can robustly cluster individual CSPs, co-cluster two or more CSPs, or segregate different CSPs into distinct compartments on cell surfaces. These tools will enable the dissection of complicated cell-signaling landscapes with high precision.

摘要

细胞表面信号传导的格局极其复杂。因此,迫切需要强大的工具来操纵细胞表面蛋白(CSP)的时空分布,以剖析信号传导。一些CSP是通过多价驱动的液-液相分离(LLPS)来调节的。利用LLPS的稳健性和通用性,我们决定设计基于LLPS的工具来精确操纵CSP。我们通过将多价模块化相分离支架对与CSP结合剂融合,生成了膜 tethering LLPS系统。支架对的相分离、CSP在膜上的伴随区室化以及CSP的簇依赖性信号输出需要一个或两个支架的膜募集。我们还设计了正交相分离系统,以将CSP分离到相互排斥的区室中。工程化的相分离系统可以稳健地聚集单个CSP、共同聚集两个或更多CSP,或将不同的CSP分离到细胞表面的不同区室中。这些工具将能够高精度地剖析复杂的细胞信号传导格局。

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