Membrane transport protein
A membrane transport protein is a membrane protein involved in the movement of ions, small molecules, and macromolecules, such as another protein, across a biological membrane. Transport proteins are integral transmembrane protein; that is they exist permanently within and span the membrane across which they transport substances. The proteins may assist in the movement of substances by facilitated diffusion or active transport. The two main types of proteins involved in such transport are broadly categorized as either channels or carriers. The solute carriers and atypical SLCs are secondary active or facilitative transporters in humans. Collectively membrane transporters and channels are transportome. Transportomes govern cellular influx and efflux of not only ions and nutrients but drugs as well.
Difference between channels and carriers
A carrier is not open simultaneously to both the extracellular and intracellular environments. Either its inner gate is open, or outer gate is open. In contrast, a channel can be open to both environments at the same time, allowing the molecules to diffuse without interruption. Carriers have binding sites, but pores and channels do not. When a channel is opened, millions of ions can pass through the membrane per second, but only 100 to 1000 molecules typically pass through a carrier molecule in the same time. Each carrier protein is designed to recognize only one substance or one group of very similar substances. Research has correlated defects in specific carrier proteins with specific diseases.Active transport
is the movement of a substance across a membrane against its concentration gradient. This is usually to accumulate high concentrations of molecules that a cell needs, such as glucose or amino acids. If the process uses chemical energy, such as adenosine triphosphate, it is called primary active transport. Secondary active transport involves the use of an electrochemical gradient, and does not use energy produced in the cell. Unlike channel proteins which only transport substances through membranes passively, carrier proteins can transport ions and molecules either passively through facilitated diffusion, or via secondary active transport. A carrier protein is required to move particles from areas of low concentration to areas of high concentration. These carrier proteins have receptors that bind to a specific molecule needing transport. The molecule or ion to be transported must first bind at a binding site at the carrier molecule, with a certain binding affinity. Following binding, and while the binding site is facing the same way, the carrier will capture or occlude the substrate within its molecular structure and cause an internal translocation so that the opening in the protein now faces the other side of the plasma membrane. The carrier protein substrate is released at that site, according to its binding affinity there.Facilitated diffusion
is the passage of molecules or ions across a biological membrane through specific transport proteins and requires no energy input. Facilitated diffusion is used especially in the case of large polar molecules and charged ions; once such ions are dissolved in water they cannot diffuse freely across cell membranes due to the hydrophobic nature of the fatty acid tails of the phospholipids that make up the bilayers.The type of carrier proteins used in facilitated diffusion is slightly different from those used in active transport. They are still transmembrane carrier proteins, but these are gated transmembrane channels, meaning they do not internally translocate, nor require ATP to function. The substrate is taken in one side of the gated carrier, and without using ATP the substrate is released into the cell. They may be used as potential biomarkers.
Reverse diffusion
, or transporter reversal, is a phenomenon in which the substrates of a membrane transport protein are moved in the opposite direction to that of their typical movement by the transporter. Transporter reversal typically occurs when a membrane transport protein is phosphorylated by a particular protein kinase, which is an enzyme that adds a phosphate group to proteins.Types
1: Channels/pores
- α-helical protein channels such as voltage-gated ion channel, ligand-gated ion channels
- β-barrel porins such as aquaporin
- channel-forming toxins, including colicins, diphtheria toxin, and others
- Nonribosomally synthesized channels such as gramicidin
- Holins; which function in export of enzymes that digest bacterial cell walls in an early step of cell lysis.
Note:
- Channels:
- than what is required to move the green circles so the movement is coupled and some energy is cancelled out. One example is the lactose permease which allows protons to go down its concentration gradient into the cell while also pumping lactose into the cell.Pores:
2: Electrochemical potential-driven transporters
Also named carrier proteins or secondary carriers.- 2.A: Porters, SLCs.
- *. One example is GLUT1 which moves glucose down its concentration gradient into the cell.Excitatory amino acid transporters
- ** EAAT1
- ** EAAT2
- ** EAAT3
- ** EAAT4
- ** EAAT5
- * Glucose transporter
- * Monoamine transporters, including:
- ** Dopamine transporter
- ** Norepinephrine transporter
- ** Serotonin transporter
- ** Vesicular monoamine transporters
- * Adenine nucleotide translocator
- 2.B: Nonribosomally synthesized porters, such as:
- * The Nigericin family
- * The Ionomycin family
- 2.C: Ion-gradient-driven energizers
3: Primary active transporters
- 3.A: P-P-bond-hydrolysis-driven transporters :
- * ATP-binding cassette transporter, such as MDR, CFTR
- * V-type ATPase ;.
- * P-type ATPase ;, such as :
- ** Na+/K+-ATPase
- ** Plasma membrane Ca2+ ATPase
- ** Proton pump
- * than what is required to move the blue circles so the movement is coupled and some energy is cancelled out. One example is the sodium-proton exchanger which allows protons to go down their concentration gradient into the cell while pumping sodium out of the cell.F-type ATPase;, including: mitochondrial ATP synthase, chloroplast ATP synthase1
- 3.B: Decarboxylation-driven transporters
- 3.C: Methyltransfer-driven transporters
- 3.D: Oxidoreduction-driven transporters
- 3.E: Light absorption-driven transporters, such as rhodopsin
4: Group translocators