F5 og F6. Membrantransport og Membranpotentialet Flashcards

1
Q

make a comparison of ion concentrations inside and outside a typical mammalian cell

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2
Q

Draw a glucose Na+ symport that uses the electrochemical Na+ gradient to drive the active import of glucose

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3
Q

Draw a typical ion channel that flutuates between closed and open conformations

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4
Q

Draw and explain why a typical neuron has a cell body, a single axon, and multiple dendrites

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5
Q

draw an electrochemical gradient that has two components and explan your drawing

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6
Q

Draw an ion channel that has a selectively filter that controls which inorganic ions it will allow to cross the membrane

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7
Q

Draw an animal and plant cell which use a variety of transmembrane pumps to drive the active transport of solutes

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8
Q

Explain how cell membranes contain specialized membrane transort proteins that facilitate the passage of selected small, water-soluble molecules

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9
Q

show how cells use different tactics to avoid osmotic swelling

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10
Q

Show how conformational changes in a transporter mediae the passive transport of a solute such as glucose

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11
Q

Draw different types of gated ion channels and show how they respond to different types of stimuli

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12
Q

Draw how each cell membrane has its own characteristic set of transporters

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13
Q

Draw gradient-driven pumps and show how they can act as symptorts or antiports

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14
Q

Show how inorganic ions and small, polar organic molecules can cross a cell membrane through either a transporter or a channel

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15
Q

Explain why mechanically-gated ion channels allow us to hear

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16
Q

Describe how a patch-clamp recording is used to monitor ion channel activity

17
Q

Show how pumps carry out active transport in three main ways

18
Q

Show how solutes cross membranes by either passive or active transport

19
Q

Show some examples of transmembrane pumps

20
Q

Draw the behavoir of a single ion channel and show how it can be observed using the patch-clamp technique

21
Q

Show how the ca2+ pump in the sarcoplasmic reticulum was the first ATP-driven ion pump to have its three-dimensional structure determined by x-ray crystallography

22
Q

Show how the distribution of ions on either side of a cell membrane gives rise to its membrane potential

23
Q

explain why the k+ concentration gradient and k+ leak channels play major parts in generating the resting membrane potential across the plasma membrane in animal cells

24
Q

Explain why the Na+ pump undergoes a series of conformational changes as it exchanges Na+ ions for K+

25
Explain why the na+ pump uses the energy of ATP hydrolysis to pump NA+ out of animal cells and k+
26
Describe how the nernst equation can be used to calculate the contribution of each ion to the resting potential of the membrane
27
Explain why the rate at which a solute crosses a protein-free, artifical lipid bilayer by simple diffusion depends on its size and solubility
28
Describe how the two types of glucose transporters enable gut epithelial cells to transfer glucose across the epithelial lining of the gut
29
Describe how water molecules diffuse rapidly through aquaporin channels in the plasma membrane of some cells
30
Essential concepts
• 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.