• The lipid bilayer of cell membranes is highly permeable to small, nonpolar molecules such as oxygen and carbon dioxide and, to a lesser extent, to very small, polar molecules such as water. It is highly impermeable to most large, water-soluble molecules and to all ions.
• Transfer of nutrients, metabolites, and inorganic ions across cell
membranes depends on membrane transport proteins.
- Cell membranes contain a variety of transport proteins that function either as transporters or channels, each responsible for the transfer of a particular type of solute.
- Channel proteins form pores across the lipid bilayer through which solutes can passively diffuse.
• Both transporters and channels can mediate passive transport, in
which an uncharged solute moves spontaneously down its concentration gradient.
• For the passive transport of a charged solute, its electrochemical
gradient determines its direction of movement, rather than its concentration gradient alone.
- Transporters can act as pumps to mediate active transport, in which solutes are moved uphill against their concentration or electrochemical gradients; this process requires energy that is provided by ATP hydrolysis, a downhill flow of Na+ or H+ ions, or sunlight.
- Transporters transfer specific solutes across a membrane by undergoing conformational changes that expose the solute-binding site first on one side of the membrane and then on the other.
- The Na+ pump in the plasma membrane of animal cells is an ATPase; it actively transports Na+ out of the cell and K+ in, maintaining a steep Na+ gradient across the plasma membrane that is used to drive other active transport processes and to convey electrical signals.
- Ion channels allow inorganic ions of appropriate size and charge to cross the membrane. Most are gated and open transiently in response to a specific stimulus.
• Even when activated by a specific stimulus, ion channels do not
remain continuously open: they flicker randomly between open and closed conformations. An activating stimulus increases the proportion of time that the channel spends in the open state.
• The membrane potential is determined by the unequal distribution of charged ions on the two sides of a cell membrane; it is altered when these ions flow through open ion channels in the membrane.
• In most animal cells, the negative value of the resting membrane
potential across the plasma membrane depends mainly on the K+
gradient and the operation of K+-selective leak channels; at this resting potential, the driving force for the movement of K+ across the membrane is almost zero.
- Neurons produce electrical impulses in the form of action potentials, which can travel long distances along an axon without weakening. Action potentials are propagated by voltage-gated Na+ and K+ channels that open sequentially in response to depolarization of the plasma membrane.
- Voltage-gated Ca2+ channels in a nerve terminal couple the arrival of an action potential to neurotransmitter release at a synapse. Transmitter-gated ion channels convert this chemical signal back into an electrical one in the postsynaptic target cell.
- Excitatory neurotransmitters open transmitter-gated cation channels that allow the influx of Na+, which depolarizes the postsynaptic cell’s plasma membrane and encourages the cell to fire an action potential. Inhibitory neurotransmitters open transmitter-gated Cl– channels in the postsynaptic cell’s plasma membrane, making it harder for the membrane to depolarize and fire an action potential.
• Complex sets of nerve cells in the human brain exploit all of the
above mechanisms to make human behaviors possible.