Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.
Institute of Inorganic Chemistry I, Ulm University, Albert-Einstein-Allee 11, 89081 Ulm, Germany.
J Am Chem Soc. 2020 Sep 16;142(37):15780-15789. doi: 10.1021/jacs.0c05261. Epub 2020 Sep 2.
Synthetic assembly within living cells represents an innovative way to explore purely chemical tools that can direct and control cellular behavior. We use a simple and modular platform that is broadly accessible and yet incorporates highly intricate molecular recognition, immolative, and rearrangement chemistry. Short bimodular peptide sequences undergo a programmed sequence of events that can be tailored within the living intracellular environment. Each sequential stage of the pathways beginning with the cellular uptake, intracellular transport, and localization imposes distinct structural changes that result in the assembly of fibrillar architectures inside cells. The observation of apoptosis, which is characterized by the binding of Annexin V, demonstrates that programmed cell death can be promoted by the peptide assembly. Higher complexity of the assemblies was also achieved by coassembly of two different sequences, resulting in intrinsically fluorescent architectures. As such, we demonstrate that the in situ construction of architectures within cells will broaden the community's perspective toward how structure formation can impact a living system.
在活细胞内进行人工合成组装代表了一种探索能够指导和控制细胞行为的纯化学工具的创新方法。我们使用一种简单而模块化的平台,该平台广泛适用,同时包含高度复杂的分子识别、消耗和重排化学。短双模块肽序列经历一个可以在活细胞内环境中定制的程序化事件序列。从细胞摄取、细胞内运输和定位开始的途径的每个连续阶段都会引起不同的结构变化,从而导致细胞内纤维状结构的组装。细胞凋亡的观察表明,细胞程序性死亡可以通过肽组装来促进。通过两种不同序列的共组装,还实现了更高的组装复杂性,从而产生了内源性荧光结构。因此,我们证明了在细胞内原位构建结构将拓宽人们对结构形成如何影响生命系统的认识。