https://www.selleckchem.com/products/blasticidin-s-hcl.html Nature uses self-organized spatiotemporal patterns to construct systems with robustness and flexibility. Furthermore, understanding the principles underlying self-organization in nature enables programmable design of artificial patterns driven by chemical energy. The related mechanisms are however not clearly understood because most of these patterns are formed in reaction-diffusion (RD) systems consisting of intricate interaction between diffusion and reaction. Therefore, comprehensive understanding of the pattern formation may provide critical knowledge for developing novel strategies in both natural science and chemical engineering. Liesegang patterns (LPs) are one of the typical programmable patterns. This study demonstrates that appropriate tuning of gel concentration distribution is a key programming factor for controlling LP periodicities. The gel distribution was realized in bi- or multilayered gels constructed by stacking agarose gels of different concentrations. Thus, exceptional LP periodicities were achieved locally in bilayered gels. Furthermore, RD simulations revealed that the nucleation process modulated by the gel distribution determines the LP periodicity in bilayered gels. Finally, based on this concept, desired LP periodicities were successfully realized by programming gel distributions in multilayered gels. Thus, deep insights into the fundamental role of nucleation in designing LPs can lead to the practical applications of LPs and the understanding of self-organization in nature.A detailed understanding of forces guiding the rapid folding of a polypeptide from an apparently random coil state to an ordered α-helical structure following the rate-limiting preorganization of the initial three residue backbones into helical conformation is imperative to comprehending and regulating protein folding and for the rational design of biological mimetics. However, several details of this process a