We present here the work we pursue in the Laboratoire Jean Perrin (CNRS - UPMC) ie. developing an "artificial morphogenesis" through DNA-based molecular programming and kinesin/microtubule active matter. We join the lab in March 2015. Previously we were working in the Laboratoire de Photonique et de Nanostructures, now Center for Nanosciences and Nanotechnology.
Figure 1: A "life-like" material through reaction-diffusion patterning. A molecular program based on short DNA strands and enzymes is able to read and interpret a pre-existing gradient of immobile DNA to generate several chemically distinct zones. As for cells in an embryo, the fate of DNA-coated beads (translated into a level of aggregation) depends on the position. More information here.
Figure 2: Active matter locally converts chemical energy into mechanical work and, for this reason, it provides new mechanisms of pattern formation. In particular, active nematic fluids made of protein motors and filaments are far-from-equilibrium systems that may exhibit spontaneous motion. We demonstrated that a 3D solution of kinesin motors and microtubule filaments can also spontaneously form a 2D free-standing nematic active sheet that actively buckles out-of-plane into a centimeter-sized periodic corrugated sheet that is stable for days. More information here.
Figure 3: A combination of self-organizating mechanisms. Here, we conjugate the two out-of-equilibrium patterning mechanisms we use - reaction-diffusion and active matter - to mimick key aspects of the polarization mechanism observed in C. elegans oocytes. A mechano-chemical transduction is produced: the microtubules-based active matter contracts globally, triggering a DNA-based reaction-diffusion front. More information here.