1 Voltage-Gated Ion Channel: Activation States Li + Ca 2+,Cl -,K +, Na + -Channels In the closed resting state, the cell membrane is polarized, the extracellular.

Slides:



Advertisements
Similar presentations
Molecular Targets For Drug Action (syllabus - prof.Kršiak) FOUR MAJOR TARGETS FOR DRUGS: 1. RECEPTORS 2. ION CHANNELS 3. CARRIER MOLECULES 4. ENZYMES.
Advertisements

Chloride Ion Channels Alexander Chew Florida State University BSC5936 February 2005.
Understanding Transport through Membranes. The importance of ion transport through membranes Water is an electrically polarizable substance, which means.
Ion Channels The plasma membrane is 6-8nm thick, and consists of a mosaic of lipids and proteins. The lipid is hydrophobic, and will not allow ions through.
Gated Ion Channels Ahu Karademir Andrei Vasiliev.
Receptors & Signaling. Assumed Knowledge Structure of membrane proteins Ion concentrations across membranes Second messengers in signal transduction Regulation.
AP Bio: Chp.11 Cell Communication. G-protein-linked receptors: vary in their binding sites and for recognizing different G-proteins. Most have seven alpha.
Inhibitory and Excitatory Signals
Lecture 20: Membrane Transport Energetics of Transmembrane Transport Active Transport Passive Transport.
PHL 211 Pharmacology Sixth Lecture By Abdelkader Ashour, Ph.D. Phone:
1 © Patrick An Introduction to Medicinal Chemistry 3/e Chapter 6 PROTEINS AS DRUG TARGETS: RECEPTOR STRUCTURE & SIGNAL TRANSDUCTION Part 1: Sections 6.1.
Lecture 05 – Extracellular Signal Receptors III Lecture 05 – Extracellular Signal Receptors III BIOL 5190/6190 Cellular & Molecular Singal Transduction.
Chapter 10 Membrane Transport Chapter 10 Membrane Transport Biochemistry I Dr. Loren Williams Biochemistry I Dr. Loren Williams Revised 03/11/2013.
BIOCHEMICAL REGULATION (2) DR SAMEER FATANI. Energetics of membrane transport systems the change in free energy when an unchanged molecules Moves from.
Cell Membranes Animal cells have a cell membrane that separates them from the environment Cell membranes are phospholipid bilayers with associated proteins.
Nervous System: Part III What Happens at a Synapse?
See also the NOTE GUIDES posted online on the wiki, the online self-quizzes posted on the wiki, and USG pages 6 to 10. Main Content: 1. Sodium Potassium.
Molecular Targets For Drug Action (syllabus -prof.Kršiak) FOUR MAJOR TARGETS FOR DRUGS: 1. RECEPTORS 2. ION CHANNELS 3. CARRIER MOLECULES 4. ENZYMES.
MARION COPELAND AND LYNNETTE LACEK FIRST YEAR MEDICAL STUDENTS PENN STATE HERSHEY COLLEGE OF MEDICINE The Action Potential and Neurotransmission.
Active Transport, Transmembrane Proteins, and Neurons AP Biology 2006.
University of Jordan1 Receptors Functions and Signal Transduction- L3 Faisal I. Mohammed, MD, PhD.
KAPITOLA 12 Interakce a regulace metabolismu vzájemné vztahy metabolických drah vzájemné vztahy metabolických drah uzlové body metabolismu uzlové body.
Evolutionary History of Ion Channels and Neurotransmitters Neuro Journal Club, Peter HANTZ, Arendt Laboratory.
Cell. Cell metabolism. The main functions of the cell 1. Basic unit of life. The cell is the smallest part to which an organism can be reduced that still.
11-2. LIGAND OR CHEMICAL GATE Voltage-Gated Channel Example: Na + channel Figure 11.6b.
Manifestation of Novel Social Challenges of the European Union in the Teaching Material of Medical Biotechnology Master’s Programmes at the University.
Voltage gated channels Molecular structure –Na +, K +, Ca ++ –Cl - Voltage sensing Action potential Calcium signaling.
Nervous Systems Part 3 RA # 4.3. What is a synapse?  Gaps between neurons or between neurons and effectors.
Transmembrane receptor (Handout) prof. aza. Transmembrane receptors are integral membrane proteins, which reside and operate typically within a cell's.
The Action Potential. Four Signals Within the Neuron  Input signal – occurs at sensor or at points where dendrites are touched by other neurons.  Integration.
AP Biology Nervous Systems Part 3. Synapse and Neurotransmitter.
Tetraodotoxin (fish) Saxitoxin (dinoflagellate-red tide) -blocks sodium channels -75 deaths/year in Japan X more potent than cocaine -little bit.
1 Back to Biochemistry… diffusion (passive, through PLBL) facilitative diffusion (passive, through channels) channels come in several flavors: ligand-gated.
Neurophysiology pages I. Resting Potential All neural activity begins with a change in the resting membrane potential of a neuron The resting.
Muscle Contraction Chapter 9 Part B. How does the anatomical structure function physiologically? What is the importance of the membranes? Why is it important.
Electrical Properties of the Nervous System Lundy-Ekman, Chapter 2 D. Allen, Ph.D.
Cellular Signaling Section 2-3. Discussion Points: What happened? How did you recognize where to go? How does this model cell communication? What effect.
Ions channels definition of ion channels: A protein that acts as a pore in a cell membrane and permits the selective passage of ions (such as potassium.
Neuron.
Pharmacodynamics III Receptor Families
Structure and function of voltage-gated Na+ channels. A
Copyright © 2017 McGraw-Hill Education. All rights reserved
ION CHANNELS AS DRUG TARGETS & CONTROL OF RECEPTOR EXPRESSION
Dr. Ahmad Al-Zohyri Dept. of Pharmacology Baghdad College of Medicine
An Introduction to Medicinal Chemistry 3/e PROTEINS AS DRUG TARGETS:
Transmembrane and GPCR Mohammed Mohammed Khan PhD Scholar- Department of Biochemistry King Abdul-Aziz University.
Neurons, Synapses, and Signaling
Sudden cardiac death: A matter of faulty ion channels?
Schematics of GABAA receptor structure and function.
بسم الله الرحمن الرحیم دانشگاه علوم پزشکی قزوین 1394
On the measurement of the functional properties of the CFTR
Molecular biology of K+ channels and their role in cardiac arrhythmias1  Martin Tristani-Firouzi, MD, Jun Chen, MD, John S Mitcheson, PhD, Michael C Sanguinetti,
From Ionic Currents to Molecular Mechanisms
M. Chincholkar  British Journal of Anaesthesia 
An Unaltered Orthosteric Site and a Network of Long-Range Allosteric Interactions for PNU in α7 Nicotinic Acetylcholine Receptors  Christopher B.
Calcium channel structure and ligand binding sites.
Pharmacodynamic Dr. Hashem Mansour.
Crystal Structures of a Ligand-free MthK Gating Ring: Insights into the Ligand Gating Mechanism of K+ Channels  Sheng Ye, Yang Li, Liping Chen, Youxing.
A Gating Mechanism of the Serotonin 5-HT3 Receptor
Kim Fisher, PhD, Terence J Coderre, PhD, Neil A Hagen, MD, FRCPC 
Chapter 18 GABA Copyright © 2012, American Society for Neurochemistry. Published by Elsevier Inc. All rights reserved.
Quickening the Pace Neuron
Structural Models of the KtrB, TrkH, and Trk1,2 Symporters Based on the Structure of the KcsA K+ Channel  Stewart R. Durell, H. Robert Guy  Biophysical.
An Introduction to Medicinal Chemistry 3/e PROTEINS AS DRUG TARGETS:
Read Chapter 5. Today: - membranes that line body cavities
Intracellular Signaling
Action Potential.
Week 4b: Ion channel structure
Week 4b: Ion channel structure
P.Thr287Pro mutation in the β2 subunit and γ-aminobutyric acid-A (GABAA) receptor is shown. p.Thr287Pro mutation in the β2 subunit and γ-aminobutyric acid-A.
Presentation transcript:

1 Voltage-Gated Ion Channel: Activation States Li + Ca 2+,Cl -,K +, Na + -Channels In the closed resting state, the cell membrane is polarized, the extracellular portion of the pore is closed while the intracellular gating mechanism remains open. Upon activation, the membrane depolarizes, opening the extracellular portion of the pore and allowing the ion to enter the cell. The refractory period occurs while the membrane is still depolarized, the gating mechanism has closed the intracellular portion of the pore, rendering the channel inactive.

2 Ligand-Gated Ion Channel: Structure and Activation States A)The intrinsic ion channel in this superfamily of receptors undergoes a conformational change following the binding of an extracellular ligand to its binding site, which allows for the opening of the channel pore. B)The pore is formed by a pentameric arrangement of subunits, which are in turn composed of a large extracellular domain (which contains the ligand binding site) and four transmembrane domains. Li + nAcChR, Serotonin, GABA A R, incl.

3 Calcium Channel Structure A)The  1 subunit is comprised of four homologous domains, each of which contains six transmembrane helices. The  subunit is intracellular and associates with the  1 subunit. The  subunit is a glyoprotein that possesses four transmembrane segments. The  2 subunit is extracellular, highly glycosylated and associates with the membrane spanning  subunit via disulfide bonds. B)The four domains of the  1 subunit cluster in the membrane to form the pore region. Li +

4 Schematic Representation of the HCN Channel Li + -Hyperpolarization-Activated CyclicNucleotide-Gated- Cation-Channel ( Na +,K + )

5 2TM Potassium Channel Structure 6TM Potassium Channel Structure Li + Four of these subunits cluster to form the active channel. Each subunit is composed of two membrane-spanning helices connected by a P loop. A)A) The  subunit is formed from 6 transmembrane segments and is associated with a regulatory  subunit. B) Four  subunits form the pore.

6 Sodium Channel Structure Li + A) The  subunit consists of four domains of six transmembrane segments, with the 5th and 6th segments comprising the pore formation unit. The  subunits consist of a single membrane spanning segment with an immunoglobulin-like fold in an extracellular domain. The  subunit contains the binding sites for a variety of toxins and drugs, as indicated. B) The four domains of the  subunit form the pore within the membrane.