The conformational change exposes two potassium binding sites on the extracellular surface of the pump Depending on the source of energy primary transport is differentiated from secondary transport. Primary transport uses energy directly: light or chemical energy is converted to electrochemical energy as electrochemical potential of the substances to be transported. This category comprises photosynthetic electron transport, light driven ion pumps, redoxenergy dependent respiratory chains, transport ATPases and sodium pumps utilizing decarboxylation energy.
In secondary transport the electrochemical energy originates from the electrochemical potential of another substance that is used up in symport or antiport.
Normally a molecule passes the membrane unchanged. However, in group translocation there is a chemical modification. This method is used by bacteria in the phosphoenolpyruvate:sugar phosphotransferase system (PTS).
Transport systems for nutrients are directed into the cell; all prokaryotic as well as eukaryotic cells contain additionally systems with a reverse transport direction to get rid of toxic substances. These systems may severely impair therapeutic efforts (multidrug efflux systems). Special transport systems protect producers of antibiotics or toxins against their own poisons.
The structures of few transport systems are known at atomic resolution. Among these are rhodopsins, some components of the PTS, and binding proteins used by bacteria in conjunction with transport ATPases. Binding proteins are found anchored to the cytoplasmic membrane of Gram-positive bacteria or free in the periplasm of Gram-negative bacteria (binding protein dependent transporters), they belong to the superfamily of ABC (ATP bindig cassette) transporters. Sugar specific binding proteins may change their conformation considerably upon binding a ligand, as the maltose binding protein of E. coli:
MBP without substrate
Glu45 Tyr 341
domain I domain IIMBP with maltoseMBP with maltotrioseExamples shown here are the binding proteins involved with the transport of maltodextrins and mercury, for proton transport a bacteriorhodopsin and components of the glucose PTS from E. coli. As an exemption from the rule there is FhuA, which is an energy dependent transport system located in the outer membrane of E. coli specific for siderophor bound iron and misused for antibiotics, phage DNA and colicins. Click the structure icons for details.
Which component is responsible for active transport?
For the most part, carrier proteins mediate active transport while channel proteins mediate passive transport. Carrier proteins create an opening in the lipid bilayer by undergoing a conformational change upon the binding of the molecule.
What is required for active transport?
Active transport requires specialized carrier proteins and the expenditure of cellular energy. Carrier proteins allow chemicals to cross the membrane against a concentration gradient or when the phospholipid bilayer of the membrane is impermeable to a chemical (Fig. 1).
Which processes are involved in active transport?
The active transport of small molecules or ions across a cell membrane is generally carried out by transport proteins that are found in the membrane. Larger molecules such as starch can also be actively transported across the cell membrane by processes called endocytosis and exocytosis.
What are 3 proteins associated with active transport?
Channel proteins, gated channel proteins, and carrier proteins are three types of transport proteins that are involved in facilitated diffusion. A channel protein, a type of transport protein, acts like a pore in the membrane that lets water molecules or small ions through quickly.