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action or later. Please see Debugging in WordPress for more information. (This message was added in version 6.7.0.) in /home/youdoctor/public_html/wp-includes/functions.php on line 6114A rich variety of channels has been isolated and analyzed from a wide range of cell membranes. Invariably intrinsic proteins, they contain numerous\u00a0amino acid<\/a>\u00a0sequences that\u00a0traverse<\/a>\u00a0the membrane, clearly forming a specific hole, or pore. Certain channels open and close spontaneously. Some are gated, or opened, by the chemical action of a signaling substance such ascalcium<\/a>,\u00a0acetylcholine<\/a>, or\u00a0glycine<\/a>, whereas others are gated by changes in the electrical potential across the membrane. Channels may possess a narrow specificity, allowing passage of only\u00a0potassium<\/a>\u00a0or\u00a0sodium<\/a>, or a broad specificity, allowing passage of all positively charged ions (cations<\/a>) or of all negatively charged ions (anions<\/a>). There are channels called gap junctions that allow the passage of\u00a0<\/span>molecules<\/a>\u00a0between pairs of cells (see below<\/em>\u00a0The cell matrix and cell-to-cell communication<\/a>).<\/p>\n The gating of channels with a capacity for\u00a0<\/span>ion<\/a>\u00a0transport is the basis of the many nerve-nerve, nerve-muscle, and nerve-gland interactions underlying neurobiological behaviour. These actions depend on the\u00a0electric potential<\/a>\u00a0of the cell membrane, which varies with the prevailing\u00a0constituents<\/a>\u00a0in the cell\u2019senvironment<\/a>. For example, if a channel that admits only potassium ions is present in a membrane separating two different potassium chloride solutions, the positively charged potassium ions tend to flow down their concentration gradient through the channel. The negatively charged chloride ions remain behind. This separation of electric charges sets up an electric potential across the membrane called the\u00a0diffusion<\/a>potential. The size of this potential depends on, among other factors, the difference in concentrations of the permeating ion across the membrane. The cell membrane in general contains the channels of widely different ion specificities, each channel contributing to the overall membrane potential according to the permeability and concentration ratio of the ion passing through it. Since the channels are often gated, the membrane\u2019s potential is determined by which channels are open; this in turn depends on the concentrations of signaling molecules and may change with time according to the membrane potential itself.<\/p>\n Most cells have about a tenfold higher concentration of sodium ions outside than inside and a reverse concentration ratio of potassium ions. Free calcium ions can be 10,000 times more concentrated outside the cell than inside. Thus, sodium-, potassium-, and calcium-selective membrane channels, by allowing the diffusion of those ions past the cell membrane and causing fluctuations in the membrane\u2019s electric potential, frequently serve as transmitters of signals from nerve cells. Ion diffusion threatens to alter the concentration of ions necessary for the cell to function. The proper distribution of ions is restored by the action of ion pumps (see below<\/em>\u00a0Primary active transport<\/a>).<\/p>\n \u062c\u0648 \u0679\u0627\u067e\u06a9 \u067e\u0691\u06be\u0646\u0627 \u0686\u0627\u06c1\u062a\u06d2 \u06c1\u06cc\u06ba \u0627\u0633 \u067e\u0631 \u06a9\u0644\u06a9 \u06a9\u0631\u06cc\u06ba<\/p> Many water-soluble molecules that cannot penetrate the lipid bilayer are too large to fit through open channels. In this category are sugars and amino acids. Some ions too do not diffuse through channels. These vital substances enter and leave the cell through the action of membrane transporters, which, like channels, are intrinsic proteins that traverse the cell membrane. Unlike channels, transporter molecules do not simply open holes in the membrane. Rather, they present sites on one side of the membrane to which molecules bind through chemical attraction. The binding site is highly specific, often fitting the atomic structure of only one type of\u00a0molecule<\/a>. When the molecule has attached to the binding site, then, in a process not fully understood, the transporter brings it through the membrane and releases it on the other side.<\/p>\n This action is considered a type of diffusion because the transported molecules move down their concentration gradients, from high concentration to low. To activate the action of the transporter, no other energy is needed than that of the chemical binding of the transported molecules. This action upon the transporter is similar to catalysis, except that the molecules (in this\u00a0context<\/a>\u00a0called substrates) catalyze not a\u00a0chemical reaction<\/a>but their own translocation across the cell membrane. Two such substrates are\u00a0<\/span>glucose<\/a>\u00a0and the bicarbonate ion.<\/p>\n This sugar-specific transport system enables half of the glucose present inside the cell to leave within four seconds at normal body temperature. The glucose transporter is clearly not a simple\u00a0membrane channel<\/a>. First, unlike a channel, it does not select its permeants by size, as one type of glucose is observed to move through the system a thousand times faster than its identically sized optical isomer. Second, it operates much more slowly than do most channels, moving only 1,000 molecules per second while a channel moves 1,000,000 ions. The most important difference between a membrane channel and the glucose transporter is the conformational change that the transporter undergoes while moving glucose across the membrane. Alternating between two conformations, it moves its glucose-binding site from one side of the membrane to the other. By \u201cflipping\u201d between its two conformational states, the transporter\u00a0facilitates<\/a>\u00a0the diffusion of glucose; that is, it enables glucose to avoid the barrier of the cell membrane while moving spontaneously down its concentration gradient. When the concentration reaches\u00a0equilibrium<\/a>, net movement of glucose ceases.<\/p>\n A\u00a0facilitated<\/a>\u00a0diffusion system for glucose is present in many cell types. Similar systems transporting a wide range of other substrates (e.g., different sugars, amino acids,\u00a0nucleosides<\/a>, and ions) are also present.<\/p>\n <\/p>\n The best-studied of the facilitated diffusion systems is that which catalyzes the exchange of anions across the\u00a0red blood cell<\/a>membrane. The exchange of hydroxyl for bicarbonate ions, each ion simultaneously being moved down its concentration gradient in opposite directions by the same transport molecule, is of great importance in\u00a0enhancing<\/a>\u00a0the blood\u2019s capacity to carry\u00a0carbon dioxide<\/a>\u00a0from tissues to the\u00a0lungs<\/a>. The exchange molecule for these anions is the major intrinsic\u00a0protein<\/a>\u00a0of red blood cells; one million of them are present on each cell, the polypeptide chain of each molecule traversing the membrane at least six times.<\/p>\n","protected":false},"excerpt":{"rendered":" A rich variety of channels has been isolated and analyzed from a wide range of cell membranes. Invariably<\/p>\n","protected":false},"author":7,"featured_media":4794,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[561],"tags":[607,554,564,558,606],"class_list":["post-4790","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-dhms-1st-year-biology","tag-about-cell","tag-biology","tag-cell","tag-dhms","tag-dhms-1st-year-biology"],"yoast_head":"\nFacilitated diffusion<\/span><\/h2>\n
The glucose transporter<\/span><\/h2>\n
The\u00a0<\/span>anion<\/a>\u00a0transporter<\/span><\/h2>\n