American Journal of Advanced Drug Delivery Open Access

  • ISSN: 2321-547X
  • Journal h-index: 22
  • Journal CiteScore: 9.36
  • Journal Impact Factor: 5.76
  • Average acceptance to publication time (5-7 days)
  • Average article processing time (30-45 days) Less than 5 volumes 30 days
    8 - 9 volumes 40 days
    10 and more volumes 45 days

Review Article - (2020) Volume 8, Issue 4


Kushal Nandi1, Dhrubo Jyoti Sen1*, Dhananjoy Saha1, Sampa Dhabal2, Beduin Mahanti1, Bhukya Bhagwan1

1Department of Pharmaceutical Chemistry, School of Pharmacy, Techno India University,Kolkata,West Bengal, India

2Forensic Scientist, Kolkata, West Bengal, India.

Corresponding Author:
Dhrubo Jyoti Sen
Department of Pharmaceutical Chemistry
School of Pharmacy, Techno India University
Kolkata, West Bengal, India

Received Date: 06-11-2020; Accepted Date: 20-11-2020; Published Date: 27-11-2020

Visit for more related articles at American Journal of Advanced Drug Delivery


Ion channels are pore–forming membrane proteins that allow ions to pass through the channel pore. Their functions include establishing a resting membrane potential, shaping action potentials and other electrical signals by gating the flow of ions across the cell membrane, controlling the flow of ions across secretory and epithelial cells, and regulating cell volume. Ion channels are present in the membranes of all cells. Ion channels are one of the two classes of ionophoric proteins, the other being ion transporters. The study of ion channels often involves biophysics, electrophysiology, and pharmacology, while using techniques including voltage clamp, patch clamp, immunohistochemistry, X–ray crystallography, fluoroscopy, and RT–PCR. Their classification as molecules is referred to as channelomics. The fundamental properties of currents mediated by ion channels were analyzed by the British biophysicists Alan Hodgkin and Andrew Huxley as part of their Nobel Prize–winning research on the action potential, published in 1952. They built on the work of other physiologists, such as Cole and Baker's research into voltage–gated membrane pores from 1941. The existence of on channels was confirmed in the 1970s by Bernard Katz and Ricardo Miledi using noise analysis. It was then shown more directly with an electrical recording technique known as the "patch clamp", which led to a Nobel Prize to Erwin Neher and Bert Sakmann, the technique's inventors. Hundreds if not thousands of researchers continue to pursue a more detailed understanding of how these proteins work. In recent years the development of automated patch clamp devices helped to increase significantly the throughput in ion channel screening.

The Nobel Prize in Chemistry for 2003 was awarded to Roderick MacKinnon for his studies on the physico–chemical properties of ion channel structure and function, including x–ray crystallographic structure studies.


ATP, RT–PCR, Biophysics, Ion channel, Action potential, XRD


There are two distinctive features of ion channels that differentiate them from other types of ion transporter proteins:

1.The rate of ion transport through the channel is very high (often 106 ions per second or greater).

2.Ions pass through channels down their electrochemical gradient, which is a function of ion concentration and membrane potential, "downhill", without the input (or help) of metabolic energy (e.g. ATP, co–transport mechanisms, or active transport mechanisms).[1]

Ion channels are located within the membrane of all excitable cells, and of many intracellular organelles. They are often described as narrow, water–filled tunnels that allow only ions of a certain size and/or charge to pass through. This characteristic is called selective permeability. The archetypal channel pore is just one or two atoms wide at its narrowest point and is selective for specific species of ion, such as sodium or potassium. However, some channels may be permeable to the passage of more than one type of ion, typically sharing a common charge: positive (cations) or negative (anions). Ions often move through the segments of the channel pore in single file nearly as quickly as the ions move through free solution. In many ion channels, passage through the pore is governed by a "gate", which may be opened or closed in response to chemical or electrical signals, temperature, or mechanical force.[2]

Ion channels are integral membrane proteins, typically formed as assemblies of several individual proteins. Such "multi–subunit" assemblies usually involve a circular arrangement of identical or homologous proteins closely packed around a water–filled pore through the plane of the membrane or lipid bilayer. For most voltage–gated ion channels, the pore–forming subunit(s) are called the α subunit, while the auxiliary subunits are denoted β, γ, and so on.(Figure 1)


Figure 1: Selectivity filter allowing only potassium ions through the potassium channel


Because channels underlie the nerve impulse and because "transmitter–activated" channels mediate conduction across the synapses, channels are especially prominent components of the nervous system. Indeed, numerous toxins that organisms have evolved for shutting down the nervous systems of predators and prey (e.g., the venoms produced by spiders, scorpions, snakes, fish, bees, sea snails, and others) work by modulating ion channel conductance and/or kinetics. In addition, ion channels are key components in a wide variety of biological processes that involve rapid changes in cells, such as cardiac, skeletal, and smooth muscle contraction, epithelial transport of nutrients and ions, T–cell activation and pancreatic beta–cell insulin release. In the search for new drugs, ion channels are a frequent target.[3] (Figure 2)


Figure 2: Working Sight of Ion Channel (Cardiac & Skeletal Muscle)


There are over 300 types of ion channels just in the cells of the inner ear. Ion channels may be classified by the nature of their gating, the species of ions passing through those gates, the number of gates (pores) and localization of proteins.

Further heterogeneity of ion channels arises when channels with different constitutive subunits give rise to a specific kind of current. Absence or mutation of one or more of the contributing types of channel subunits can result in loss of function and, potentially, underlie neurologic diseases.[4]

Classification by gating

Ion channels may be classified by gating, i.e. what opens and closes the channels. For example, voltage–gated ion channels open or close depending on the voltage gradient across the plasma membrane, while ligand–gated ion channels open or close depending on binding of ligands to the channel.[5] (Figure 3)


Figure 3: Voltage Gated Sodium Channel

Voltage–gated sodium channels: This family contains at least 9 members and is largely responsible for action potential creation and propagation. The pore–forming α subunits are very large (up to 4,000 amino acids) and consist of four homologous repeat domains (I–IV) each comprising six transmembrane segments (S1–S6) for a total of 24 transmembrane segments. The members of this family also assembled with auxiliary β subunits, each spanning the membrane once. Both α and β subunits are extensively glycosylated.

Voltage–gated calcium channels: This family contains 10 members, though these are knownto coassemble with α2δ, β, and γ subunits. These channels play an important role in both linking muscle excitation with contraction as well as neuronal excitation with transmitter release. The α subunits have an overall structural resemblance to those of the sodium channels and are equally large.[6] (Figure 4)


Figure 4: Voltage Gated Calcium Channel

Cation channels of sperm: This small family of channels, normally referred to as Catsper channels, is related to the two–pore channels and distantly related to TRP channels.(Figure 5)


Figure 5: Cation Channels of Sperms

Voltage–gated potassium channels (KV):This family contains almost 40 members, which are further divided into 12 subfamilies. These channels are known mainly for their role in repolarizing the cell membrane following action potentials. The α subunits have six transmembrane segments, homologous to a single domain of the sodium channels. Correspondingly, they assemble as tetramers to produce a functioning channel.[7] (Figure 6)


Figure 6: Voltage Gated Potassium Channel

Some transient receptor potential channels: This group of channels, normally referred to simply as TRP channels, is named after their role in Drosophila phototransduction. This family, containing at least 28 members, is incredibly diverse in its method of activation. Some TRP channels seem to be constitutively open, while others are gated by voltage, intracellular Ca2+, pH, redox state, osmolarity, and mechanical stretch. These channels also vary according to the ion(s) they pass, some being selective for Ca2+ while others are less selective, acting as cation channels. This family is subdivided into 6 subfamilies based on homology: classical (TRPC), vanilloid receptors (TRPV), melastatin (TRPM), polycystins (TRPP), mucolipins (TRPML), and ankyrin transmembrane protein 1 (TRPA).

Hyperpolarization–activated cyclic nucleotide– gated channels: The opening of these channels is due to hyperpolarization rather than the depolarization required for other cyclic nucleotide–gated channels.These channels are also sensitive to the cyclic nucleotides cAMP and cGMP, which alter the voltage sensitivity of the channel's opening. These channels are permeable to the monovalent cations K+ and Na+. There are 4 members of this family, all of which form tetramers of six–transmembrane α subunits. As these channels open under hyperpolarizing conditions, they function as pacemaking channels in the heart, particularly the SA node.[8] (Figure 7)


Figure 7: Hyperpolarization–activated cyclic nucleotide–gated channels

Voltage–gated proton channels: Voltage–gated proton channels open with depolarization, but in a strongly pH– sensitive manner. The result is that these channels open only when the electrochemical gradient is outward, such that their opening will only allow protons to leave cells. Their function thus appears to be acid extrusion from cells. Another important function occurs in phagocytes (e.g. eosinophils, neutrophils, macrophages) during the "respiratory burst." When bacteria or other microbes are engulfed by phagocytes, the enzyme NADPH oxidase assembles in the membrane and begins to produce reactive oxygen species (ROS) that help kill bacteria. NADPH oxidase is electrogenic, moving electrons across the membrane, and proton channels open to allow proton flux to balance the electron movement electrically. [9] (Figure 8)


Figure 8: Voltage gated proton channel

Ligand–gated (neurotransmitter): Also known as ionotropic receptors, this group of channels open in response to specific ligand molecules binding to the extracellular domain of the receptor protein. Ligand binding causes a conformational change in the structure of the channel protein that ultimately leads to the opening of the channel gate and subsequent ion flux across the plasma membrane. Examples of such channels include the cation–permeable "nicotinic" Acetylcholine receptor, ionotropic glutamate–gated receptors, acid sensing ion channels (ASICs), ATP–gated P2X receptors, and the anion–permeable γ–aminobutyric acid–gated GABAA receptor.

Ion channels activated by second messengers may also be categorized in this group, although ligands and second messengers are otherwise distinguished from each other. [10] (Figure 9)


Figure 9: Ionotropic Receptor

Lipid–gated: This group of channels opens in response to specific lipid molecules binding to the channel's transmembrane domain typically near the inner leaflet of the plasma membrane. Phosphatidylinositol 4,5– bisphosphate (PIP2) and phosphatidic acid (PA) are the best–characterized lipids to gate these channels. Many of the leak potassium channels are gated by lipids including the inward–rectifier potassium channels and two pore domain potassium channels TREK–1 and TRAAK. KCNQ potassium channel family are gated by PIP2. The voltage activated potassium channel (Kv) is regulated by PA. Its midpoint of activation shifts +50 mV upon PA hydrolysis, near resting membrane potentials. This suggests Kv could be opened by lipid hydrolysis independent of voltage and may qualify this channel as dual lipid and voltage gated channel.[11] (Figure 10)


Figure 10: Liquid and voltage gated ion channels

Other gating

Gating also includes activation and inactivation by second messengers from the inside of the cell membrane – rather than from outside the cell, as in the case for ligands.

Some potassium channels

Inward–rectifier potassium channels: These channels allow potassium ions to flow into the cell in an "inwardly rectifying" manner: potassium flows more efficiently into than out of the cell. This family is composed of 15 official and 1 unofficial member and is further subdivided into 7 subfamilies based on homology. These channels are affected by intracellular ATP, PIP2, and G–protein βγ subunits. They are involved in important physiological processes such as pacemaker activity in the heart, insulin release, and potassium uptake in glial cells. They contain only two transmembrane segments, corresponding to the core pore–forming segments of the KV and KCa channels. Their α subunits form tetramers.[12] (Figure 11)


Figure 11: Inward–rectifier potassium channels

Calcium–activated potassium channels: This family of channels is activated by intracellular Ca2+ and contains 8 members.(Figure 12)


Figure 12: Calcium activated potassium channels

Tandem pore domain potassium channel: This family of 15 members form what are known as leak channels, and they display Goldman–Hodgkin–Katz (open) rectification. Contrary to their common name of 'Two–pore–domain potassium channels', these channels have only one pore but two pore domains per subunit.

Two–pore channels include ligand–gated and voltage– gated cation channels, so–named because they contain two pore–forming subunits. As their name suggests, they have two pores. Light–gated channels like channel rhodopsin are directly opened by photons.[13]

Mechanosensitive ion channels open under the influence of stretch, pressure, shear, and displacement.(Figure 13)


Figure 13: Tandem pore domain potassium channel

Cyclic nucleotide–gated channels: This superfamily of channels contains two families: the cyclic nucleotide– gated (CNG) channels and the hyperpolarization–activated, cyclic nucleotide–gated (HCN) channels. This grouping is functional rather than evolutionary

Cyclic nucleotide–gated channels: This family of channels is characterized by activation by either intracellular cAMP or cGMP. These channels are primarily permeable to monovalent cations such as K+ and Na+. They are also permeable to Ca2+, though it acts to close them. There are 6 members of this family, which is divided into 2 subfamilies. Hyperpolarization–activated cyclic nucleotide–gated channels.(Figure 14)


Figure 14: Cyclic nucleotide–gated channels

Temperature–gated channels: Members of the transient receptor potential ion channel superfamily, such as TRPV1 or TRPM8, are opened either by hot or cold temperatures.

Classification by type of ions

Chloride channels: This superfamily of channels consists of approximately 13 members. They include ClCs, CLICs, Bestrophins and CFTRs. These channels are non–selective for small anions; however chloride is the most abundant anion, and hence they are known as chloride channels.

Potassium channels

• Voltage–gated potassium channels e.g., Kvs, Kirs etc.

• Calcium–activated potassium channels e.g., BKCa or MaxiK, SK, etc.

• Inward–rectifier potassium channels

• Two–pore–domain potassium channels: This family of 15 members form what is known as leak channels, and they display Goldman–Hodgkin– Katz (open) rectification.

• Sodium channels: Voltage–gated sodium channels (NaVs)

• Epithelial sodium channels (ENaCs)

• Calcium channels (CaVs)

• Proton channels

• Voltage–gated proton channels

• Non–selective cation channels: These non–selectively allow many types of cations, mainly Na+, K+ and Ca2+, through the channel.

• Most transient receptor potential channels

Classification by cellular localization

Ion channels are also classified according to their subcellular localization. The plasma membrane accounts for around 2% of the total membrane in the cell, whereas intracellular organelles contain 98% of the cell's membrane. The major intracellular compartments are endoplasmic reticulum, Golgi apparatus, and mitochondria. On the basis of localization, ion channels are classified as:

Plasma membrane channels: Examples: Voltage–gated potassium channels (Kv), Sodium channels (Nav), Calcium channels (Cav) and Chloride channels (ClC). Intracellular channels, which are further classified into different organelles.

Endoplasmic reticulum channels: RyR, SERCA, ORAi Mitochondrial channels: mPTP, KATP, BK, IK, CLIC5, Kv7.4 at the inner membrane and VDAC and CLIC4 as outer membrane channels.

Other classifications

Some ion channels are classified by the duration of their response to stimuli:

Transient receptor potential channels: This group of channels, normally referred to simply as TRP channels, is named after their role in Drosophila visual phototransduction. This family, containing at least 28 members, is diverse in its mechanisms of activation. Some TRP channels remain constitutively open, while others are gated by voltage, intracellular Ca2+, pH, redox state, osmolarity, and mechanical stretch. These channels also vary according to the ion(s) they pass, some being selective for Ca2+ while others are less selective cation channels. This family is subdivided into 6 subfamilies based on homology: canonical TRP (TRPC), vanilloid receptors (TRPV), melastatin (TRPM), polycystins (TRPP), mucolipins (TRPML), and ankyrin transmembrane protein 1 (TRPA).[14]

Detailed structure

Channels differ with respect to the ion they let pass (for example, Na+, K+, Cl), the ways in which they may be regulated, the number of subunits of which they are composed and other aspects of structure. Channels belonging to the largest class, which includes the voltage–gated channels that underlie the nerve impulse, consists of four subunits with six transmembrane helices each. On activation, these helices move about and open the pore. Two of these six helices are separated by a loop that lines the pore and is the primary determinant of ion selectivity and conductance in this channel class and some others. The existence and mechanism for ion selectivity was first postulated in the late 1960s by Bertil Hille and Clay Armstrong. The idea of the ionic selectivity for potassium channels was that the carbonyl oxygens of the protein backbones of the "selectivity filter" (named by Bertil Hille) could efficiently replace the water molecules that normally shield potassium ions, but that sodium ions were smaller and cannot be completely dehydrated to allow such shielding, and therefore could not pass through. This mechanism was finally confirmed when the first structure of an ion channel was elucidated. A bacterial potassium channel KcsA, consisting of just the selectivity filter, "P" loop and two transmembrane helices was used as a model to study the permeability and the selectivity of ion channels in the Mackinnon lab. The determination of the molecular structure of KcsA by Roderick MacKinnon using X–ray crystallography won a share of the 2003 Nobel Prize in Chemistry.

Because of their small size and the difficulty of crystallizing integral membrane proteins for X–ray analysis, it is only very recently that scientists have been able to directly examine what channels "look like." Particularly in cases where the crystallography required removing channels from their membranes with detergent, many researchers regard images that have been obtained as tentative. An example is the long–awaited crystal structure of a voltage–gated potassium channel, which was reported in May 2003. One inevitable ambiguity about these structures relates to the strong evidence that channels change conformation as they operate (they open and close, for example), such that the structure in the crystal could represent any one of these operational states. Most of what researchers have deduced about channel operation so far they have established through electrophysiology, biochemistry, gene sequence comparison and mutagenesis.

Channels can have single (CLICs) to multiple transmembrane (K channels, P2X receptors, Na channels) domains which span plasma membrane to form pores. Pore can determine the selectivity of the channel. Gate can be formed either inside or outside the pore region.[15]


Chemical substances can modulate the activity of ion channels, for example by blocking or activating them.

Ion channel blockers

A variety of ion channel blockers (inorganic and organic molecules) can modulate ion channel activity and conductance. Some commonly used blockers include:

1. Tetrodotoxin (TTX), used by puffer fish and some types of newts for defence. It blocks sodium channels.

2. Saxitoxin is produced by a dinoflagellate also known as "red tide". It blocks voltage–dependent sodium channels.

3. Conotoxin is used by cone snails to hunt prey.

4. Lidocaine and Novocaine belong to a class of local anesthetics which block sodium ion channels.

5. Dendrotoxin is produced by mamba snakes, and blocks potassium channels.

6. Iberiotoxin is produced by the Buthus tamulus (Eastern Indian scorpion) and blocks potassium channels.

7. Heteropodatoxin is produced by Heteropoda venatoria (brown huntsman spider or laya) and blocks potassium channels.

Ion channel activators

Several compounds are known to promote the opening or activation of specific ion channels. These are classified by the channel on which they act:

1. Calcium channel openers, such as Bay K8644

2. Chloride channel openers, such as phenanthroline

3. Potassium channel openers, such as minoxidil

4. Sodium channel openers, such as DDT


There are a number of disorders which disrupt normal functioning of ion channels and have disastrous consequences for the organism. Genetic and autoimmune disorders of ion channels and their modifiers are known as channelopathies. Shaker gene mutations cause a defect in the voltage gated ion channels, slowing down the repolarization of the cell. Equine hyperkalaemic periodic paralysis as well as human hyperkalaemic periodic paralysis (HyperPP) are caused by a defect in voltage–dependent sodium channels. Paramyotonia congenita (PC) and potassium–aggravated myotonias (PAM). Generalized epilepsy with febrile seizures plus (GEFS+). Episodic ataxia (EA), characterized by sporadic bouts of severe discoordination with or without myokymia, and can be provoked by stress, startle, or heavy exertion such as exercise. Familial hemiplegic migraine (FHM). Spinocerebellar ataxia type 13. Long QT syndrome is a ventricular arrhythmia syndrome caused by mutations in one or more of presently ten different genes, most of which are potassium channels and all of which affect cardiac repolarization. Brugada syndrome is another ventricular arrhythmia caused by voltage–gated sodium channel gene mutations. Polymicrogyria is a developmental brain malformation caused by voltage–gated sodium channel and NMDA receptor gene mutations. Cystic fibrosis is caused by mutations in the CFTR gene, which is a chloride channel. Mucolipidosis type IV is caused by mutations in the gene encoding the TRPML1 channel. Mutations in and overexpression of ion channels are important events in cancer cells. In Glioblastoma multiforme, upregulation of gBK potassium channels and ClC–3 chloride channels enable glioblastoma cells to migrate within the brain, which may lead to the diffuse growth patterns of these tumors.[16] (Figure 15)


Figure 15: CT Scan & MRI

Radiopharmaceuticals are a special class of drugs. They include diagnostic agents, such as molecular imaging probes, contrast agents or tracers, as well as agents that treat diseases, called radio therapeutics. A radiopharmaceutical contains a radioactive isotope that emits energy, which can be detected or used to provide an image (diagnostic agent) or is directly therapeutic within a diseased tissue. Millions of patients receive radiopharmaceuticals annually for a wide variety of medical procedures ranging from the assessment of cardiac function to staging and treatment of cancer. Diagnostic radiopharmaceuticals are administered to a patient and enable physicians and researchers to non– invasively see the biochemical activity of cells, to diagnose or stage disease, identify which patients are best suited for a particular treatment, and help monitor a patient’s response to treatment. The imaging probes selectively locate at the site of disease, and release positrons or gamma rays that can be detected and digitally imaged with specialized cameras, producing images through positron emission tomography (PET) or single photon emission computed tomography (SPECT). The probes accumulate at the site of disease and the images appear as colored or dark regions in partial or whole–body structural images provided by computed tomography (CT) or magnetic resonance imaging (MRI). Community Preservation and Development Corporation (CPDC) currently markets and distributes diagnostic radiopharmaceuticals and is providing next generation imaging probes for our partners’ clinical trials. Therapeutic radiopharmaceuticals are administered to a patient to selectively seek out and deliver cell–killing radiation to the site of disease. These drugs are designed to bind selectively to specific biochemical protein receptors on or within cells at the site of the disease. Therapeutic radiopharmaceuticals can take many forms including highly selective proteins and antibodies, peptides or small molecules.[17] (Figure 16)


Figure 16: X–Ray

An X–ray, or X–radiation, is a penetrating form of high– energy electromagnetic radiation. Most X–rays have a wavelength ranging from 10 picometers to 10 nanometers, corresponding to frequencies in the range 30 petahertz to 30 exahertz (3×1016 Hz to 3×1019 Hz) and energies in the range 124 eV to 124 keV. X–ray wavelengths are shorter than those of UV rays and typically longer than those of gamma rays. In many languages, X–radiation is referred to as Röntgen radiation, after the German scientist Wilhelm Röntgen, who discovered it on November 8, 1895[1]. He named it X–radiation to signify an unknown type of radiation.(Figure 17)


Figure 17: Pacemaker

A cardiac pacemaker (or artificial pacemaker, so as not to be confused with the natural pacemaker of the heart), is a medical device that generates electrical impulses delivered by electrodes to cause the heart muscle chambers (the upper, or atria and/or the lower, or ventricles) to contract and therefore pump blood; by doing so this device replaces and/or regulates the function of the electrical conduction system of the heart. The primary purpose of a pacemaker is to maintain an adequate heart rate, either because the heart's natural pacemaker is not fast enough, or because there is a block in the heart's electrical conduction system. Modern pacemakers are externally programmable and allow a cardiologist, particularly a cardiac electrophysiologist to select the optimal pacing modes for individual patients. A specific type of pacemakers called defibrillator combines pacemaker and defibrillator functions in a single implantable device, which should be called only defibrillator, for clarity. Others, called biventricular pacemakers have multiple electrodes stimulating differing positions within the lower heart chambers to improve synchronization of the ventricles, the lower chambers of the heart.[18]


Chemical engineering deals with chemistry and chemistry is a word made of chemist+try so it follows the pathway of why, when, where & how the four coins to tell try–try–try until you get the result. Chemical engineering follows unit operation chapter which in related fields, a unit operation is a basic step in a process. Unit operations involve a physical change or chemical transformation such as separation, crystallization, evaporation, filtration, polymerization, isomerization, and other reactions. For example, in milk processing, homogenization, pasteurization, and packaging are each unit operations which are connected to create the overall process. A process may require many unit operations to obtain the desired product from the starting materials, or feedstocks. Same chemistry in unit operation is procured in body system by in–vivo where separation (blood filtration through kidney, air purification by lungs alveoli, perspiration through sweat gland/apocrine gland), crystallisation (deposition in adipose tissue), evaporation (perspiration through skin), filtration (glomerular filtration through nephron), polymerization (macromolecular enzymes, polypeptides, lipopolysaccharides, phospholipids, lipoproteins, ATP), isomerization (zwitterion formation by amino acids).