Ligand Path: A Software Tool for Mapping Dynamic Ligand Migration Channel Networks

AbstractProteins are essential compositions of the living organisms and involved in the processes of different life events. Basically proteins are like amazing tiny bio-machines performing the functions in a stable and predictable manner and understanding the underline mechanisms can facilitate the pharmaceutical development. However, protein functions are not carried in a static style, so experimental observations of these dynamic movements of the drugs inside the proteins are difficult, so computational methods have an important and irreplaceable role.We developed a software tool called LigandPath for mapping the ligand migration channels in a constantly moving protein and this software can function with CADD (Computer aided drug design) software to map the possible migration pathways of candidate drugs inside a protein. Traditionally, biologists use MD (Molecular Dynamics) simulation to locate the ligand migration channels, but it takes long time for them to observe the complete migration paths. In order to overcome the limitations of the trajectory-based MD simulation, we adopt a computational method inspired from robotic motion planning called DyME (Dynamic Map Ensemble) and we develop the software tool LigandPath based on DyME. The software tool has already been successfully applied to map the potential migration channels of drugs candidates of three proteins, PPAR (peroxisome proliferator-activated receptors), UROD (uroporphyrinogen decarboxylase) and Sirt1 (silent information regulator 1) complexes in three publications

Magnon dark modes and gradient memory

Extensive efforts have been expended in developing hybrid quantum systems to overcome the short coherence time of superconducting circuits by introducing the naturally long-lived spin degree of freedom. Among all the possible materials, single-crystal yttrium iron garnet has shown up very recently as a promising candidate for hybrid systems, and various highly coherent interactions, including strong and even ultra-strong coupling, have been demonstrated. One distinct advantage of these systems is that the spins are in the form of well-defined magnon modes, which allows flexible and precise tuning. Here we demonstrate that by dissipation engineering, a non-Markovian interaction dynamics between the magnon and the microwave cavity photon can be achieved. Such a process enables us to build a magnon gradient memory to store information in the magnon dark modes, which decouple from the microwave cavity and thus preserve a long life-time. Our findings provide a promising approach for developing long-lifetime, multimode quantum memories.Comment: 18 pages, 12 figure