Mutations for monogenic epilepsies have been found primarily in genes coding
for ion channels 32 as well as in two different proteins that may be involved in neurogenesis 33.
And potassium
for ion channels.
Not exact matches
The major U.S. broadcast television networks have affiliates in the Oklahoma City market (ranked 41st
for television by Nielsen and 48th
for radio by Arbitron, covering a 34 - county area serving the central, north - central and west - central sections of Oklahoma); including NBC affiliate KFOR - TV (
channel 4), ABC affiliate KOCO - TV (
channel 5), CBS affiliate KWTV - DT (
channel 9, the flagship of locally based Griffin Communications), PBS station KETA - TV (
channel 13, the flagship of the state - run OETA member network), Fox affiliate KOKH - TV (
channel 25), CW affiliate KOCB (
channel 34), independent station KAUT - TV (
channel 43), MyNetworkTV affiliate KSBI - TV (
channel 52), and
Ion Television owned - and - operated station KOPX - TV (
channel 62).
His team has been working on making systems that mimic natural
ion channels,
for example, but much bigger so that they can transport entire molecules.
It was commissioned by Roderick MacKinnon, who shared the Nobel prize in 2003
for his work describing the structural and mechanistic properties of such
channels, which are tunnels that regulate the flow of
ions across cellular membranes.
Unlike the existing reverse - osmosis membranes responsible
for more than half of the world's current water desalination capacity, the new membrane process dehydrates
ions as they pass through the membrane
channels and removes only select
ions, rather than indiscriminately removing all
ions.
These findings demonstrate that the ability of the
channel to adapt its structure differently to K + and Na + is a fundamental aspect of
ion selectivity, as is the ability of multiple K +
ions to compete effectively with Na +
for the conductive filter.
BK
channels are potassium
ion channels found on the surface of a variety of cell types that are essential
for the regulation of several key physiological processes, including smooth muscle tone and neuronal excitability.
«Synthetic proteins help solve structure of the fluoride
ion channel: Unexpected double - barreled «channsporter» structure suggests new mechanism
for ion transport.»
The ability to specifically block the
ion channel with monobodies also raises intriguing possibilities
for translational applications.
Fluoride
ion channels have only recently been discovered, and studies have hinted at an unusual structure that might explain their remarkable selectivity
for fluoride.
For the fluoride ion channel, the surface area that is covered by detergent compounds proved to be too much for crystal formation to occur, due to the channel's small size and almost complete embedment within the membra
For the fluoride
ion channel, the surface area that is covered by detergent compounds proved to be too much
for crystal formation to occur, due to the channel's small size and almost complete embedment within the membra
for crystal formation to occur, due to the
channel's small size and almost complete embedment within the membrane.
Eddaoudi and his collaborators overcame this problem with their design of Cr - soc - MOF - 1, a MOF made up of chromium
ions linked together by carboxylate - based organic ligands that leave well - defined cages and
channels for water to collect.
Hence AMPA and NMDA receptor
channels contain common structural motifs in their TM2 segments that are responsible
for some of their
ion selectivity and conductance properties.
Researchers experimented with different configurations
for their remote control system, and they found the best relies on an iron nanoparticle (blue), which is tethered by a protein (green) to an
ion channel (red).
Four HCN genes that code
for proteins which form
ion channels in neurons could be involved, because these
channels are vital
for electrical signalling in nerves.
The study, conducted by two teams at Duke University and appearing online Dec. 1 in the journal Neuron, is the first to connect autism to one of the most well - studied pain molecules, called TRPV1 (transient receptor potential
ion channel subtype V1), which is a receptor
for the main spicy component of chili peppers.
The mutation resulted in a lower single
channel conductance
for calcium and a strongly increased conductance
for sodium and potassium, indicating that glutamic acid - 95 is a crucial constituent of the
ion selectivity filter.
Specifically, the bipolar neurons expressed more genes
for membrane receptors and
ion channels than non-bipolar cells, particularly those receptors and
channels involved in the sending and receiving of calcium signals between cells.
Ion channels are generally selective
for certain
ions, allowing specific types of
ions to flow through at very high rates, while hindering the flow of others.
The cell's most ubiquitous gateways are potassium
ion channels — the importance of this type of
ion channels was underpinned in 2003 when Roderick MacKinnon received the Nobel Prize in Chemistry
for resolving the first atomic structure of the bacterial KcsA potassium
channel.
Researchers at Johns Hopkins have spotted a strong family trait in two distant relatives: The
channels that permit entry of sodium and calcium
ions into cells turn out to share similar means
for regulating
ion intake, they say.
For example, cardiologists would be delighted to have human cardiomyocytes in culture bearing mutations in specific
ion channels.
Researchers have known
for decades that some microorganisms, such as single - celled green algae, have proteins that respond to light by opening a
channel in the microbe's membranes, allowing the passage of electrically charged
ions (such as calcium and sodium).
Professor Asif Ahmed, Pro-Vice-Chancellor
for Health and Professor of Vascular Biology at Aston University, said: «Our latest research highlights that compounds that deliver low levels of carbon monoxide can block specific
ion channels in the heart muscle to allow the muscle time to contract properly and forcefully in a coordinated fashion.
It uses a virus already approved by the Food & Drug Administration
for other genetic therapies in the eye; it delivers an
ion channel gene similar to one normally found in humans, unlike others that employ genes from other species; and it can easily be reversed or adjusted by supplying new chemical photoswitches.
The receptor or
ion channel, called TRPV1, was originally discovered in sensory neurons, where it acts as a sentinel
for heat, acidity and spicy chemicals in the environment.
The therapy employs a virus to insert a gene
for a common
ion channel into normally blind cells of the retina that survive after the light - responsive rod and cone photoreceptor cells die as a result of diseases such as retinitis pigmentosa.
For years, scientists have been unsure how calcium
ion channels function.
«From the clinical point of view, DENAQ is a great advance on AAQ, because it acts specifically on a particular type of
ion channel that is essential
for the transmission of signals received from the rods and cones,» says Trauner.
When the IP3R calcium
channel receives signals, it creates a pathway
for calcium
ions to move across cell membranes.
The researchers studied calcium
channels in neurons, which allow
for the transport of calcium
ions from one nerve cell to another, helping the cells transmit itch signals from the skin to other cells in the spinal cord.
Importantly, they observed a significant disruption of the assembly of the axon initial segment (AIS), a subcellular structure in the proximal part of the axon important
for clustering of
ion channels, and thus,
for neurons to fire action potentials.
Whereas in the nematode experiment the researchers targeted nanoparticles to temperature - sensitive
ion channels that naturally exist in the membranes of the worms» nerve cells, the scientists inserted the gene
for a heat - activated
ion channel called TRPV1 into the human and rat cells.
For example, the identification of highly specific and potent CFTR inhibitors has led to a number of studies examining the role of CFTR
ion channel function in basic physiological processes.
A team of researchers under the direction of the University of Bonn has now discovered a new mechanism
for influencing
ion channels in epilepsy.
To get around this problem, neurobiologists Susana Lima and Gero Miesenböck of the Yale University School of Medicine in New Haven, Connecticut, inserted a gene that codes
for a rat
ion channel into Drosophila fruit flies.
If the
ion channel were expressed in the giant fiber neurons, which control reflexes
for escape, the flies could be made to leap about, buzz their wings, and fly.
Mycoplasma compete with host cells
for nutrients and can alter expression of receptors,
ion channels, and growth factors resulting in changes to the cell line's growth and behavior.
Double inverted vectors expressing light inducible
ion channels (plasmid # 20298
for example) have revolutionized Neuroscience.
Ion channels present a big opportunity
for future drug therapies.
Building on those findings, the Jans identified the genes
for a different family of
channels called calcium - activated chloride
channels, which shuttle chloride
ions to control smooth muscle contraction in the stomach, intestines, and lung airways.
Objective: To develop artificial «ionic machines»
for active manipulation and control of
ion and fluid transport through nanometric
channels, thereby imitating the functions of ionic machinery found in nature.
These broad associations with complexity are evidently superimposed on notable lineage - specific variation as seen in Fig. 4 (
for example, serine protease gene loss in C. elegans, and voltage-gated
ion channel expansion in Paramecium).
Susan Amara, USA - «Regulation of transporter function and trafficking by amphetamines, Structure - function relationships in excitatory amino acid transporters (EAATs), Modulation of dopamine transporters (DAT) by GPCRs, Genetics and functional analyses of human trace amine receptors» Tom I. Bonner, USA (Past Core Member)- Genomics, G protein coupled receptors Michel Bouvier, Canada - Molecular Pharmacology of G protein - Coupled Receptors; Molecular mechanisms controlling the selectivity and efficacy of GPCR signalling Thomas Burris, USA - Nuclear Receptor Pharmacology and Drug Discovery William A. Catterall, USA (Past Core Member)- The Molecular Basis of Electrical Excitability Steven Charlton, UK - Molecular Pharmacology and Drug Discovery Moses Chao, USA - Mechanisms of Neurotophin Receptor Signaling Mark Coles, UK - Cellular differentiation, human embryonic stem cells, stromal cells, haematopoietic stem cells, organogenesis, lymphoid microenvironments, develomental immunology Steven L. Colletti, USA Graham L Collingridge, UK Philippe Delerive, France - Metabolic Research (diabetes, obesity, non-alcoholic fatty liver, cardio - vascular diseases, nuclear hormone receptor, GPCRs, kinases) Sir Colin T. Dollery, UK (Founder and Past Core Member) Richard M. Eglen, UK Stephen M. Foord, UK David Gloriam, Denmark - GPCRs, databases, computational drug design, orphan recetpors Gillian Gray, UK Debbie Hay, New Zealand - G protein - coupled receptors, peptide receptors, CGRP, Amylin, Adrenomedullin, Migraine, Diabetes / obesity Allyn C. Howlett, USA Franz Hofmann, Germany - Voltage dependent calcium
channels and the positive inotropic effect of beta adrenergic stimulation; cardiovascular function of cGMP protein kinase Yu Huang, Hong Kong - Endothelial and Metabolic Dysfunction, and Novel Biomarkers in Diabetes, Hypertension, Dyslipidemia and Estrogen Deficiency, Endothelium - derived Contracting Factors in the Regulation of Vascular Tone, Adipose Tissue Regulation of Vascular Function in Obesity, Diabetes and Hypertension, Pharmacological Characterization of New Anti-diabetic and Anti-hypertensive Drugs, Hypotensive and antioxidant Actions of Biologically Active Components of Traditional Chinese Herbs and Natural Plants including Polypehnols and Ginsenosides Adriaan P. IJzerman, The Netherlands - G protein - coupled receptors; allosteric modulation; binding kinetics Michael F Jarvis, USA - Purines and Purinergic Receptors and Voltage-gated
ion channel (sodium and calcium) pharmacology Pain mechanisms Research Reproducibility Bong - Kiun Kaang, Korea - G protein - coupled receptors; Glutamate receptors; Neuropsychiatric disorders Eamonn Kelly, Prof, UK - Molecular Pharmacology of G protein - coupled receptors, in particular opioid receptors, regulation of GPCRs by kinasis and arrestins Terry Kenakin, USA - Drug receptor pharmacodynamics, receptor theory Janos Kiss, Hungary - Neurodegenerative disorders, Alzheimer's disease Stefan Knapp, Germany - Rational design of highly selective inhibitors (so call chemical probes) targeting protein kinases as well as protein interaction inhibitors of the bromodomain family Andrew Knight, UK Chris Langmead, Australia - Drug discovery, GPCRs, neuroscience and analytical pharmacology Vincent Laudet, France (Past Core Member)- Evolution of the Nuclear Receptor / Ligand couple Margaret R. MacLean, UK - Serotonin, endothelin, estrogen, microRNAs and pulmonary hyperten Neil Marrion, UK - Calcium - activated potassium channels, neuronal excitability Fiona Marshall, UK - GPCR molecular pharmacology, structure and drug discovery Alistair Mathie, UK - Ion channel structure, function and regulation, pain and the nervous system Ian McGrath, UK - Adrenoceptors; autonomic transmission; vascular pharmacology Graeme Milligan, UK - Structure, function and regulation of G protein - coupled receptors Richard Neubig, USA (Past Core Member)- G protein signaling; academic drug discovery Stefan Offermanns, Germany - G protein - coupled receptors, vascular / metabolic signaling Richard Olsen, USA - Structure and function of GABA - A receptors; mode of action of GABAergic drugs including general anesthetics and ethanol Jean - Philippe Pin, France (Past Core Member)- GPCR - mGLuR - GABAB - structure function relationship - pharmacology - biophysics Helgi Schiöth, Sweden David Searls, USA - Bioinformatics Graeme Semple, USA - GPCR Medicinal Chemistry Patrick M. Sexton, Australia - G protein - coupled receptors Roland Staal, USA - Microglia and neuroinflammation in neuropathic pain and neurological disorders Bart Staels, France - Nuclear receptor signaling in metabolic and cardiovascular diseases Katerina Tiligada, Greece - Immunopharmacology, histamine, histamine receptors, hypersensitivity, drug allergy, inflammation Georg Terstappen, Germany - Drug discovery for neurodegenerative diseases with a focus on AD Mary Vore, USA - Activity and regulation of expression and function of the ATP - binding cassette (ABC) transport
ion channel (sodium and calcium) pharmacology Pain mechanisms Research Reproducibility Bong - Kiun Kaang, Korea - G protein - coupled receptors; Glutamate receptors; Neuropsychiatric disorders Eamonn Kelly, Prof, UK - Molecular Pharmacology of G protein - coupled receptors, in particular opioid receptors, regulation of GPCRs by kinasis and arrestins Terry Kenakin, USA - Drug receptor pharmacodynamics, receptor theory Janos Kiss, Hungary - Neurodegenerative disorders, Alzheimer's disease Stefan Knapp, Germany - Rational design of highly selective inhibitors (so call chemical probes) targeting protein kinases as well as protein interaction inhibitors of the bromodomain family Andrew Knight, UK Chris Langmead, Australia - Drug discovery, GPCRs, neuroscience and analytical pharmacology Vincent Laudet, France (Past Core Member)- Evolution of the Nuclear Receptor / Ligand couple Margaret R. MacLean, UK - Serotonin, endothelin, estrogen, microRNAs and pulmonary hyperten Neil Marrion, UK - Calcium - activated potassium
channels, neuronal excitability Fiona Marshall, UK - GPCR molecular pharmacology, structure and drug discovery Alistair Mathie, UK -
Ion channel structure, function and regulation, pain and the nervous system Ian McGrath, UK - Adrenoceptors; autonomic transmission; vascular pharmacology Graeme Milligan, UK - Structure, function and regulation of G protein - coupled receptors Richard Neubig, USA (Past Core Member)- G protein signaling; academic drug discovery Stefan Offermanns, Germany - G protein - coupled receptors, vascular / metabolic signaling Richard Olsen, USA - Structure and function of GABA - A receptors; mode of action of GABAergic drugs including general anesthetics and ethanol Jean - Philippe Pin, France (Past Core Member)- GPCR - mGLuR - GABAB - structure function relationship - pharmacology - biophysics Helgi Schiöth, Sweden David Searls, USA - Bioinformatics Graeme Semple, USA - GPCR Medicinal Chemistry Patrick M. Sexton, Australia - G protein - coupled receptors Roland Staal, USA - Microglia and neuroinflammation in neuropathic pain and neurological disorders Bart Staels, France - Nuclear receptor signaling in metabolic and cardiovascular diseases Katerina Tiligada, Greece - Immunopharmacology, histamine, histamine receptors, hypersensitivity, drug allergy, inflammation Georg Terstappen, Germany - Drug discovery for neurodegenerative diseases with a focus on AD Mary Vore, USA - Activity and regulation of expression and function of the ATP - binding cassette (ABC) transport
Ion channel structure, function and regulation, pain and the nervous system Ian McGrath, UK - Adrenoceptors; autonomic transmission; vascular pharmacology Graeme Milligan, UK - Structure, function and regulation of G protein - coupled receptors Richard Neubig, USA (Past Core Member)- G protein signaling; academic drug discovery Stefan Offermanns, Germany - G protein - coupled receptors, vascular / metabolic signaling Richard Olsen, USA - Structure and function of GABA - A receptors; mode of action of GABAergic drugs including general anesthetics and ethanol Jean - Philippe Pin, France (Past Core Member)- GPCR - mGLuR - GABAB - structure function relationship - pharmacology - biophysics Helgi Schiöth, Sweden David Searls, USA - Bioinformatics Graeme Semple, USA - GPCR Medicinal Chemistry Patrick M. Sexton, Australia - G protein - coupled receptors Roland Staal, USA - Microglia and neuroinflammation in neuropathic pain and neurological disorders Bart Staels, France - Nuclear receptor signaling in metabolic and cardiovascular diseases Katerina Tiligada, Greece - Immunopharmacology, histamine, histamine receptors, hypersensitivity, drug allergy, inflammation Georg Terstappen, Germany - Drug discovery
for neurodegenerative diseases with a focus on AD Mary Vore, USA - Activity and regulation of expression and function of the ATP - binding cassette (ABC) transporters
Mutations
for mammoth hemoglobin, extra hair growth, fat production, down to nuanced climate adaptations such as slightly altered sodium
ion channels in cell membranes have already been engineered into fibroblast cell lines.
Hopefully these results may accelerate the development of treatments
for pain that selectively target Nav1.7 and aid drug design efforts aimed at other voltage-gated
ion channels.
His studies, ranging from molecular experiments to clinical trials, have generated comprehensive evidence
for the efficacy of omega - 3 in preventing cardiac sudden death and established the mechanism by which omega - 3 fatty acids can reduce cardiac arrhythmia by interacting with membrane
ion channels and stabilizing the electrical activity of heart cells.
Cell type - specific pharmacology
for activating genetically engineered
ion channels has been described (Slimko et al., 2002; Magnus et al., 2011), and here we demonstrate rapid cell type - specific blockade of a native
ion channel with a small molecule.
Structure of heat - sensitive
ion channel TRPV1, the receptor
for capsaicin, the active ingredient in hot chile pepper.