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Abstract:
Advanced flexible ionotronic devices have found excellent applications in the next generation of electronic skin (e-skin) development for smart wearables, robotics, and prosthesis. In this work, we developed transparent ionotronic-based flexible electrochemical capacitors using gel electrolytes and indium tin oxide (ITO) based transparent flexible electrodes. Different gel electrolytes were prepared using various salts, including NaCl, KCl, and LiCl in a 1:1 ratio with a polyvinyl alcohol (PVA) solution and compared its electrochemical performances. The interaction between gel electrolytes and ITO electrodes was investigated through the development of transparent electrochemical capacitors (TEC). The stable and consistent supply of ions was provided by the gel, which is essential for the charge storage and discharge within the TEC. The total charge contribution of the developed TECs is found from the diffusion-controlled mechanism and is measured to be 4.59 mC cm−2 for a LiCl/PVA-based gel. The prepared TEC with LiCl/PVA gel electrolyte exhibited a specific capacitance of 6.61 mF cm−2 at 10 μA cm−2. The prepared electrolyte shows a transparency of 99% at 550 nm and the fabricated TEC using LiCl/PVA gel exhibited a direct bandgap of 5.34 eV. The primary benefits of such ionotronic-based TEC development point to its potential future applications in the manufacturing of transparent batteries, electrochromic energy storage devices, ionotronic-based sensors, and photoelectrochemical energy storage devices.

Abstract:
The mitogen-activated protein kinase (MAPK) family of proteins is involved in regulating cellular fates such as proliferation, differentiation and apoptosis. In particular, the dynamics of the Erk/Mek system, which has become the canonical example for MAPK signaling systems, have attracted considerable attention. Erk is encoded by two genes, Erk1 and Erk2, that until recently had been considered equivalent as they differ only subtly at the sequence level. However, these proteins exhibit radically different trafficking between cytoplasm and nucleus and this fact may have functional implications. Here we use spatially resolved data on Erk1/2 to develop and analyze spatio-temporal models of these cascades, and we discuss how sensitivity analysis can be used to discriminate between mechanisms. Our models elucidate some of the factors governing the interplay between signaling processes and the Erk1/2 localization in different cellular compartments, including competition between Erk1 and Erk2. Our approach is applicable to a wide range of signaling systems, such as activation cascades, where translocation of molecules occurs. Our study provides a first model of Erk1 and Erk2 activation and their nuclear shuttling dynamics, revealing a role in the regulation of the efficiency of nuclear signaling.