Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, W12 0BZ London, United Kingdom.
Institute of Chemical Biology, Imperial College London, Molecular Sciences Research Hub, W12 0BZ London, United Kingdom.
Proc Natl Acad Sci U S A. 2019 Aug 20;116(34):16711-16716. doi: 10.1073/pnas.1903500116. Epub 2019 Aug 1.
To date, reconstitution of one of the fundamental methods of cell communication, the signaling pathway, has been unaddressed in the bottom-up construction of artificial cells (ACs). Such developments are needed to increase the functionality and biomimicry of ACs, accelerating their translation and application in biotechnology. Here, we report the construction of a de novo synthetic signaling pathway in microscale nested vesicles. Vesicle-cell models respond to external calcium signals through activation of an intracellular interaction between phospholipase A2 and a mechanosensitive channel present in the internal membranes, triggering content mixing between compartments and controlling cell fluorescence. Emulsion-based approaches to AC construction are therefore shown to be ideal for the quick design and testing of new signaling networks and can readily include synthetic molecules difficult to introduce to biological cells. This work represents a foundation for the engineering of multicompartment-spanning designer pathways that can be utilized to control downstream events inside an AC, leading to the assembly of micromachines capable of sensing and responding to changes in their local environment.
迄今为止,在人工细胞(AC)的自下而上构建中,尚未涉及细胞通讯的基本方法之一——信号通路的重建。这些发展对于提高 AC 的功能和仿生能力、加速其在生物技术中的转化和应用是必要的。在这里,我们报告了在微尺度嵌套囊泡中构建从头开始的合成信号通路。囊泡-细胞模型通过在内部膜中存在的磷脂酶 A2 和机械敏感通道之间的细胞内相互作用的激活来响应外部钙信号,触发隔室之间的内容混合,并控制细胞荧光。因此,基于乳液的 AC 构建方法被证明非常适合于快速设计和测试新的信号网络,并且可以很容易地包含难以引入生物细胞的合成分子。这项工作为构建能够跨越多个隔室的设计路径奠定了基础,这些路径可用于控制 AC 内的下游事件,从而组装能够感知和响应其局部环境变化的微型机器。