Rod‐Cell‐Mimetic Photochromic Layered Ion Channels with Multiple Switchable States for Controllable Ion Transport

2019 ◽  
Vol 25 (55) ◽  
pp. 12795-12800
Author(s):  
Tianliang Xiao ◽  
Jing Ma ◽  
Jiaqiao Jiang ◽  
Mengke Gan ◽  
Bingxin Lu ◽  
...  
Keyword(s):  
1986 ◽  
Vol 250 (3) ◽  
pp. F379-F385 ◽  
Author(s):  
L. G. Palmer

The patch-clamp technique of Neher and Sakmann and their colleagues has been widely used over the last 5 years to investigate ion channels in excitable tissues. More recently, it has become useful as a tool to study channels involved in transepithelial ion transport. In this review, I briefly cover the basic concepts behind the patch-clamp technique and the kinds of information that can be obtained with it. I then summarize the applications of the technique to renal tissues and describe some of the channel types that have been observed to date in epithelia.


2014 ◽  
Vol 369 (1638) ◽  
pp. 20130102 ◽  
Author(s):  
Albrecht Schwab ◽  
Christian Stock

Cell migration is a central component of the metastatic cascade requiring a concerted action of ion channels and transporters (migration-associated transportome), cytoskeletal elements and signalling cascades. Ion transport proteins and aquaporins contribute to tumour cell migration and invasion among other things by inducing local volume changes and/or by modulating Ca 2+ and H + signalling. Targeting cell migration therapeutically bears great clinical potential, because it is a prerequisite for metastasis. Ion transport proteins appear to be attractive candidate target proteins for this purpose because they are easily accessible as membrane proteins and often overexpressed or activated in cancer. Importantly, a number of clinically widely used drugs are available whose anticipated efficacy as anti-tumour drugs, however, has now only begun to be evaluated.


2004 ◽  
Vol 28 (4) ◽  
pp. 143-154 ◽  
Author(s):  
George R. Dubyak

The steady-state maintenance of highly asymmetric concentrations of the major inorganic cations and anions is a major function of both plasma membranes and the membranes of intracellular organelles. Homeostatic regulation of these ionic gradients is critical for most functions. Due to their charge, the movements of ions across biological membranes necessarily involves facilitation by intrinsic membrane transport proteins. The functional characterization and categorization of membrane transport proteins was a major focus of cell physiological research from the 1950s through the 1980s. On the basis of these functional analyses, ion transport proteins were broadly divided into two classes: channels and carrier-type transporters (which include exchangers, cotransporters, and ATP-driven ion pumps). Beginning in the mid-1980s, these functional analyses of ion transport and homeostasis were complemented by the cloning of genes encoding many ion channels and transporter proteins. Comparison of the predicted primary amino acid sequences and structures of functionally similar ion transport proteins facilitated their grouping within families and superfamilies of structurally related membrane proteins. Postgenomics research in ion transport biology increasingly involves two powerful approaches. One involves elucidation of the molecular structures, at the atomic level in some cases, of model ion transport proteins. The second uses the tools of cell biology to explore the cell-specific function or subcellular localization of ion transport proteins. This review will describe how these approaches have provided new, and sometimes surprising, insights regarding four major questions in current ion transporter research. 1) What are the fundamental differences between ion channels and ion transporters? 2) How does the interaction of an ion transport protein with so-called adapter proteins affect its subcellular localization or regulation by various intracellular signal transduction pathways? 3) How does the specific lipid composition of the local membrane microenvironment modulate the function of an ion transport protein? 4) How can the basic functional properties of a ubiquitously expressed ion transport protein vary depending on the cell type in which it is expressed?


1993 ◽  
Vol 26 (1) ◽  
pp. 1-25 ◽  
Author(s):  
E. Bamberg ◽  
H.-J. Butt ◽  
A. Eisenrauch ◽  
K. Fendler

Ion pumps create ion gradients across cell membranes while consuming light energy or chemical energy. The ion gradients are used by the corresponding cell types for passive-ion transport via ion channels or carriers or for accumulation of nutrients like sugar or amino acids via cotransport systems or antiporters.


2019 ◽  
Vol 4 (2) ◽  
pp. 239-251 ◽  
Author(s):  
Moon Jeong Park

Designs of future polymer electrolytes are linked to confinements through end-group chemistry, precise sequencing of ions, single-ion transport, and crystalline ion channels.


2010 ◽  
Vol 297-301 ◽  
pp. 1469-1474 ◽  
Author(s):  
Bogusław Bożek ◽  
Bartek Wierzba ◽  
Marek Danielewski

Ion transport across the membrane of the living cell (molecular ion channels) is a critical process, e.g., the triggering of nerve cells and heart muscle cells is coupled with mechanisms controlled by ion diffusion (electrodiffusion). Although the process is described by the century old Nernst- Planck-Poisson system of equations, it is not well understood and a clear understanding of how the interaction between channel and ions affects the flow is still missing. We present a three-dimensional model of the molecular channel. An appropriate quantitative description of the ion transport process allows proper explanation of molecule channel interactions (e.g. the ions flow for a given concentration gradient should depend on the potential and other parameters describing the interaction, i.e. asymmetric transport). We show the simulation of the stationary electrodiffusion in the ion channel showing radial symmetry.


2010 ◽  
Vol 81 (3) ◽  
Author(s):  
Punyabrata Pradhan ◽  
Yariv Kafri ◽  
Dov Levine
Keyword(s):  

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