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50 Cards in this Set

  • Front
  • Back
Which of the following statements regarding the structure and function of cell membranes is correct?
The phospholipid bilayer is arranged so that the hydrophilic heads of the phospholipid molecule face the extra- and intracellular fluids.

Some proteins integrated into the membrane function as channels associated with transport of ions through the membrane.
Diffusion
depends upon the random motion of molecules
The net flux of a penetrating solute into a cell will increase if the
permeability constant for that solute increases.

concentration of that solute in the extracellular fluid increases.
In general, polar molecules diffuse more rapidly through the lipid bilayer part of cell membranes than do nonpolar molecules. This statement is:
False. Nonpolar molecules diffuse through more rapidly because much of the bilayer is nonpolar.
Which of the following statements regarding the movement of molecules across cell membranes is correct?
The diffusion of molecules across a cell membrane occurs at a rate that is influenced by the surface area of the membrane and the magnitude of the concentration difference across it.
Which of the following statements regarding the diffusion of nonpolar solutes across cell membranes is correct?
At equilibrium for solute X, the net flux of X across cell membranes is zero.

At equilibrium for solute X, the concentration of X inside the cell is equal to its concentration outside the cell.
The permeability of the plasma membrane to mineral ions
is dependent upon channels formed by proteins.

varies from one cell to another.

is affected by differences in electrical charge on the two sides of the membrane.
Ion channels in cell membranes
may open in response to a change in potential difference across the membrane.

may open in response to binding a ligand.
The concentration of
sodium and chloride ions in the extracellular fluid is greater than that in the cytosol of cells.
Mediated transport across cell membranes
is characterized by saturable carriers and a maximum velocity of transport.
Carrier-mediated transport
involves a specific membrane protein that functions as a carrier molecule.
Which of the following is a feature that distinguishes active transport from, facilitated diffusion?
Requirement for metabolic energy
The mediated transport of a substance across a plasma membrane
depends upon the binding of that substance to a specific site on the membrane protein.
Which of the following statements regarding the active transport of molecules across cell membranes is correct?
Both primary and secondary active transport are dependent upon energy derived from ATP.
Glucose
enters most cells by diffusion.

enters most cells by active transport.

concentrations inside most cells are generally the same as those in the extra-cellular fluid.

B and C.

None of the above.
Which of the following is not a difference between primary active transport and secondary active transport ?
Primary active transport uses energy derived from ATP whereas the secondary active transport does not.
Which of the following statements regarding the active transport of solutes across cell membranes is correct?
Primary active transporters are ATPases, and secondary active transporters are not.
Secondary active transporters require binding of Na ion on the extracellular side of the membrane to transport solute either into or out of the cell.
Which of the following statements about the Na, K pump is false?
It transports Na+ and K+ in a 1:1 ratio.
It transports Na+ and K+ in a 1:1 ratio.
diffusion.
primary active transport.
secondary active transport.
Curves A, B, C, and D below represent the entry of various molecules into a cell. Therefore,
if molecule A crosses the membrane by facilitated diffusion, then curve C may represent the entry of A in the presence of a similar molecule.
If the ATP-generating mechanisms in a cell are poisoned and the cell has depleted its ATP reserves,
primary active transport of molecules would cease immediately.
eventually there will be no potential difference across the membrane.
“Osmosis” refers to the movement of across semi-permeable membranes.
water
If pure water and a solution containing a nonpenetrating solute are separated by a membrane that is permeable to water,
water will diffuse by osmosis until stopped by opposing hydrostatic pressure.
If all other conditions remain the same and the concentration of a nonpenetrating solute increases inside a cell,
water will tend to enter the cell because the interior has an increased osmolarity.
If a cell is placed in a hypotonic solution, it
will swell.
If a cell is placed in a hyperosmotic solution, it
may swell, shrink, or stay the same size, depending upon the concentration of penetrating and nonpenetrating solutes in the solution.
The reason solutions for injection or infusion into people normally contain either 150 mM NaCl or 300 mM glucose is that
these solutions are isotonic to the blood and cells.
An example of a hypertonic solution is:
400 mM urea.
Which of the following solutions is not isotonic to human cells?
300 mM urea.
Regarding the tonicity and osmolarity of solutions, which of the following statements is not true?
Isotonic solutions are always isoosmotic.
Which of the following statements regarding endocytosis and exocytosis is correct?
Endocytosis is a method by which large molecules may be brought into a cell.

Exocytosis is a method by which large molecules may be secreted from a cell.
Endocytosis is a method by which large molecules may be brought into a cell.
Exocytosis is a method by which large molecules may be secreted from a cell.
Epithelial cells are polarized.

Epithelial cells lining the small intestine have Na, K -ATPase pumps only in their basolateral membranes.
Which of the following are possible combinations of mechanisms for transport of a particle against a concentration gradient across an epithelial cell?
Passive diffusion on the apical side into the cell followed by primary active transport on the basolateral side.

Secondary active transport on the mucosal side followed by facilitated diffusion on the serosal side.
During the active transport of glucose across an epithelium, energy is used to
power the Na -glucose cotransporter.
Exocrine glands differ from endocrine glands in that the former
are formed from infoldings of embryonic epithelium whereas the latter are not.
Entry of glucose from the blood into tissue cells occurs by
osmosis
A ligand is a molecule that binds to
a protein by noncovalent bonds.
A binding site on a protein is
an area of the protein with a shape complementary to that of a ligand.

determined by the amino acid sequence of the protein.
The affinity of a ligand for its binding site is determined by
the number and position of mutually attracting electrical charges.

the number and position of mutually attracting hydrophobic surfaces.

the presence or absence of interfering or hindrance determinants.
The affinity a binding site has for a ligand
can be influenced by the shape of the binding site.

can be influenced by the presence of charged groups on the ligand and the binding site.

is a measure of how readily a bound ligand can be released from the protein.
Binding site A requires twice the concentration of ligand to achieve saturation as does binding site B. From this one can conclude that
binding site B has a higher affinity for the ligand than does binding site A.
Which of the following does not describe the 50%-saturation point of a solution of ligands and proteins?
It refers to the amount of protein required to bind 50% of the ligand.
A competitive antagonist for a ligand
blocks the binding of the ligand to its binding site and prevents activation of the protein.
Two ligands, A and B, bind to a site on protein X. Their binding curves are shown below. When ligand A binds, it produces a biological effect. Ligand B produces no effect when it binds. Therefore:
The binding site on X has a higher affinity for A than for B.

Increasing the concentration of B in the presence of A will decrease the biological effect.
Allosteric proteins
contain more than one kind of binding site.

undergo a change of shape when a ligand binds to the regulatory binding site.
The term “allosteric modulation” refers to
the change in the shape and functional state of a protein that occurs when a ligand binds to a receptor site.
When a chemical binds noncovalently to a protein at a distance from its functional site and causes a conformational change in the site that prevents the natural ligand from binding, this is an example of
allosteric modulation

noncompetitive antagonism.
Phosphorylation or dephosphorylation of proteins is a common means of
covalent modulation of the proteins.

the activation or inactivation of kinases.
Modulator molecules
bind to proteins and cause a conformational change that facilitates or inhibits the binding of the functional ligand to its binding site.
Protein kinases
are enzymes.

are allosteric.