Chapter 7 Flashcards

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1
Q

what cell ability is fundamental to life? what makes this posible

A

. The ability of the cell to discriminate in its chemical exchanges is fundamental to life, and it is the plasma membrane and its component molecules that
make this selectivity possible.

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2
Q

how are proteins distributed in the membrane and what have researchers proposed calling something related to them

A

The proteins are not randomly distributed in the membrane,
however. Groups of proteins are often associated in long-lasting,
specialized patches, where they carry out common functions.
Researchers have found specific lipids in these patches as well
and have proposed naming them lipid rafts, but there is ongoing controversy about whether such structures exist in living
cells or are an artifact of biochemical techniques.

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3
Q

Like all models, the fluid mosaic model is

A

continually being refined as new

research reveals more about membrane structure.

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4
Q

how do some memb proetins seem to move and why maybe?

A

Some membrane
proteins seem to move in a highly directed manner, perhaps
driven along cytoskeletal fibers in the cell by motor proteins connected to the membrane proteins’ cytoplasmic regions.
However, many other membrane proteins seem to be held
immobile by their attachment to the cytoskeleton or to the
extracellular matrix

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5
Q

A membrane remains fluid as temperature decreases until

A

the phospholipids settle into a closely packed arrangement
and the membrane solidifies, much as bacon grease forms lard
when it cools

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6
Q

Therefore, extreme environments pose

a challenge for

A

life, resulting in evolutionary adaptations

that include differences in membrane lipid composition.

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7
Q

integral proteins

A

Integral proteins penetrate the hydrophobic interior of the
lipid bilayer. The majority are transmembrane proteins, which
span the membrane; other integral proteins extend only partway into the hydrophobic interior. The hydrophobic regions
of an integral protein consist of one or more stretches of nonpolar amino acids (see Figure 5.14), typically 20–30 amino
acids in length, usually coiled into α helices (Figure 7.6). The
hydrophilic parts of the molecule are exposed to the aqueous
solutions on either side of the membrane. Some proteins also
have one or more hydrophilic channels that allow passage
through the membrane of hydrophilic substances (even of
water itself; see Figure 7.1

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8
Q

peripheral

A

Peripheral proteins are not
embedded in the lipid bilayer at all; they are loosely bound
to the surface of the membrane, often to exposed parts of
integral proteins

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9
Q

Furthermore, a single membrane protein may itself

carry out

A

multiple functions. Thus, the membrane is not only
a structural mosaic, with many proteins embedded in the
membrane, but also a functional mosaic, carrying out a range of fxns

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10
Q

Cell-cell recognition d and fxn

A

, a cell’s ability to distinguish one type of
neighboring cell from another, is crucial to the functioning
of an organism. It is important, for example, in the sorting
of cells into tissues and organs in an animal embryo

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11
Q

how do cels recognize other cells

A

). Cells recognize other cells by binding to

molecules, often containing carbohydrates, on the extracellular surface of the plasma membrane

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12
Q

membrane carbs- how long, what are they bonded to and called consequentyl

A

ular surface of the plasma membrane (see Figure 7.7d).
Membrane carbohydrates are usually short, branched chains
of fewer than 15 sugar units. Some are covalently bonded to
lipids, forming molecules called glycolipids. (Recall that glyco
refers to carbohydrate.) However, most are covalently bonded
to proteins, which are thereby glycoproteins (see Figure 7.3).
The carbohydrates on the extracellular side of the plasma
membrane vary from species to species, among individuals of
the same species, and even from one cell type to another in
a single individual. T

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13
Q

A transport protein is specific for

A

the substance it translocates (moves), allowing only a certain substance (or a small
group of related substances) to cross the membrane. For
example, a specific carrier protein in the plasma membrane
of red blood cells transports glucose across the membrane
50,000 times faster than glucose can pass through on its own.
This “glucose transporter” is so selective that it even rejects
fructose, a structural isomer of glucose.

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14
Q

Thus, the selective

permeability of a membrane depends on

A

both the discriminating barrier of the lipid bilayer and the specific transport
proteins built into the membrane.

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15
Q

osmosis (sugar water fake barrier example, j explan it)

A

Two sugar solutions of different
concentrations are separated by a membrane that the solvent (water)
can pass through but the solute (sugar) cannot. Water molecules
move randomly and may cross in either direction, but overall, water
diffuses from the solution with less concentrated solute to that
with more concentrated solute. This passive transport of water,
or osmosis, makes the sugar concentrations on both sides more
nearly equal. (The concentrations are prevented from being exactly
equal due to the effect of water pressure on the higher side, which
is not discussed here, for simplicity.)

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16
Q

y. Note that each substance diffuses

down its own concentration gradient, unaffected by

A

the concentration gradients of other substances

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17
Q

Much of the traffic across cell membranes occurs by diffusion. One important example is

A

the uptake of
oxygen by a cell performing cellular respiration. Dissolved
oxygen diffuses into the cell across the plasma membrane.
As long as cellular respiration consumes the O2 as it enters,
diffusion into the cell will continue because the concentration gradient favors movement in that direction.

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18
Q

osmosis across an artificial barrier

A

Two sugar solutions of different
concentrations are separated by a membrane that the solvent (water)
can pass through but the solute (sugar) cannot. Water molecules
move randomly and may cross in either direction, but overall, water
diffuses from the solution with less concentrated solute to that
with more concentrated solute. This passive transport of water,
or osmosis, makes the sugar concentrations on both sides more
nearly equal. (The concentrations are prevented from being exactly
equal due to the effect of water pressure on the higher side, which
is not discussed here, for simplicity.)

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19
Q

. However, tight clustering of water molecules
around the hydrophilic solute molecules makes some of the
water unavailable to cross the membrane. As a result

A

e solution with a higher solute concentration has a lower free water
concentration. Water diffuses across the membrane from the
region of higher free water concentration (lower solute concentration) to that of lower free water concentration (higher
solute concentration) until the solute concentrations on both
sides of the membrane are more nearly equal. The diffusion of
free water across a selectively permeable membrane, whether
artificial or cellular, is called osmosis

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20
Q

why doesnt a paramecium cell burst when it has contractile vacuole

A

. The Paramecium cell doesn’t burst because it is also
equipped with a contractile vacuole, an organelle that functions as a bilge pump to force water out of the cell as fast as it
enters by osmosis

21
Q

t, the bacteria and
archaea that live in hypersaline (excessively salty) environments
(see Figure 27.1) have cellular mechanisms that

A

balance the
internal and external solute concentrations to ensure that water
does not move out of the cell

22
Q

Plants that are not woody, such as most houseplants, depend

for mechanical support on

A

cells kept turgid by a surrounding
hypotonic solution. If a plant’s cells and surroundings are isotonic, there is no net tendency for water to enter and the cells
become flaccid (limp); the plant wilts.

23
Q

However, a cell wall is of no advantage if the cell is

immersed in a hypertonic environment

A

In this case, a plant
cell, like an animal cell, will lose water to its surroundings
and shrink

24
Q

This phenomenon is called facilitated diffusion

A

, many polar molecules and ions impeded by the lipid bilayer of the membrane
diffuse passively with the help of transport proteins that span the
membrane. T

25
Q

example of gated channels that are electrical

A

or some
gated channels, the stimulus is electrical. In a nerve cell, for
example, an ion channel opens in response to an electrical
stimulus, allowing a stream of potassium ions to leave the
cell. (See the potassium ion channel at the beginning of this
chapter.) This restores the cell’s ability to fire again

26
Q

Other
gated channels open or close when a specific substance other
than the one to be transported binds to the channel. These
gated channels are also important in

A

t in the functioning of the

nervous system

27
Q

Carrier proteins, such as the glucose transporter mentioned

earlier,

A

seem to undergo a subtle change in shape that somehow

translocates the solute-binding site across the membrane

28
Q

Such a change in shape may be triggered by

A

y the
binding and release of the transported molecule. Like ion channels, carrier proteins involved in facilitated diffusion result in the
net movement of a substance down its concentration gradient

29
Q

active transport examples and why it makes sense

A

. The
transport proteins that move solutes against their concentration gradients are all carrier proteins rather than channel
proteins. This makes sense because when channel proteins
are open, they merely allow solutes to diffuse down their
concentration gradients rather than picking them up and
transporting them against their gradients

30
Q

t. One way ATP
can power active transport is when its terminal phosphate
group is transferred directly to the transport protein

A

. This
can induce the protein to change its shape in a manner
that translocates a solute bound to the protein across the
membrane. One transport system that works this way is the
sodium-potassium pump, which exchanges Na+
for K+
across the plasma membrane of animal cells (Figure 7.15).
The distinction between passive transport and active transport is reviewed i

31
Q

The cytoplasmic side of the
membrane is negative in charge relative to the extracellular
side because

A

of an unequal distribution of anions and

cations on the two sides.

32
Q

The voltage across a membrane,

A

called a membrane potential, ranges from about -50 to
-200 millivolts (mV). (The minus sign indicates that the
inside of the cell is negative relative to the outside.)

33
Q

The membrane potential acts like

A

a battery, an energy
source that affects the traffic of all charged substances across
the membrane. Because the inside of the cell is negative compared with the outside, the membrane potential favors the
passive transport of cations into the cell and anions out of the
cell. T

34
Q

This combination of forces acting

on an ion is called the electrochemical gradient.

A

Thus, two forces drive the diffusion of ions across a membrane: a chemical force (the ion’s concentration gradient,
which has been our sole consideration thus far in the chapter)
and an electrical force (the effect of the membrane potential
on the ion’s movement)

35
Q

One important use of proton gradients

in

A

the cell is for ATP synthesis during cellular respiration, as you
will see in Concept 9.4. Another is a type of membrane traffic
called cotransport.

36
Q

cotransport example

A

For instance,
a plant cell uses the gradient of H+
generated by its ATP-powered
proton pumps to drive the active transport of amino acids,
sugars, and several other nutrients into the c

37
Q

explain what results from plant sucrose h gradient

A

l. The resulting
H+
gradient represents potential energy that can be used for active
transport—of sucrose, in this case. Thus, ATP hydrolysis indirectly
provides the energy necessary for cotransport

38
Q

what do plants do with the scursoe made from photosynth

A

The vascular tissue of the plant can then distribute the sugar to
roots and other nonphotosynthetic organs that do not make
their own food.

39
Q

why treat diarrhea with a drink of nacl and glucose

A

The solutes are taken up by sodiumglucose cotransporters on the surface of intestinal cells and
passed through the cells into the blood. This simple treatment has lowered infant mortality worldwide.

40
Q

what do exo and endo cytosis nd

A

energy

41
Q

When the vesicle membrane

and plasma membrane come into contact (during travel of a vesicle to the membrane)

A

specific proteins
rearrange the lipid molecules of the two bilayers so that the
two membranes fuse. The contents of the vesicle spill out of
the cell, and the vesicle membrane becomes part of the plasma
membrane

42
Q

rme for cholesterol: how does it travel? what happens> what is hypercholesteremia

A

Human cells use receptor-mediated endocytosis to take
in cholesterol for membrane synthesis and the synthesis of
other steroids. Cholesterol travels in the blood in particles
called low-density lipoproteins (LDLs), each a complex of
lipids and a protein. LDLs bind to LDL receptors on plasma
membranes and then enter the cells by endocytosis. In the
inherited disease familial hypercholesterolemia, characterized by a very high level of cholesterol in the blood, LDLs
cannot enter cells because the LDL receptor proteins are
defective or missing:

43
Q

what happens in hpercholesterima

A

Consequently, cholesterol accumulates in the blood,
where it contributes to early atherosclerosis, the buildup of
lipid deposits within the walls of blood vessels. This buildup
narrows the space in the vessels and impedes blood flow,
potentially resulting in heart damage and stroke.

44
Q

In phagocytosis,

A

s, a cell engulfs a particle
by extending pseudopodia (singular,
pseudopodium) around it and packaging
it within a membranous sac called a food
vacuole. The particle will be digested after the
food vacuole fuses with a lysosome containing
hydrolytic enzymes

45
Q

In pinocytosis

A

a cell continually “gulps”
droplets of extracellular fluid into tiny
vesicles, formed by infoldings of the plasma
membrane. In this way, the cell obtains
molecules dissolved in the droplets. Because
any and all solutes are taken into the cell,
pinocytosis as shown here is nonspecific for
the substances it transports. In many cases, as
above, the parts of the plasma membrane that
form vesicles are lined on their cytoplasmic
side by a fuzzy layer of coat protein; the “pits”
and resulting vesicles are said to be “coated.

46
Q

Receptor-mediated endocytosis is

A

a
specialized type of pinocytosis that enables
the cell to acquire bulk quantities of specific
substances, even though those substances
may not be very concentrated in the
extracellular fluid. Embedded in the plasma
membrane are proteins with receptor sites
exposed to the extracellular fluid. Specific
solutes bind to the receptors. The receptor
proteins then cluster in coated pits, and
each coated pit forms a vesicle containing
the bound molecules. The diagram shows
only bound molecules (purple triangles) inside
the vesicle, but other molecules from the
extracellular fluid are also present.
After the ingested material is liberated
from the vesicle, the emptied receptors are
recycled to the plasma membrane by the
same vesicle (not shown)

47
Q

Endocytosis and exocytosis also provide mechanisms for
rejuvenating or remodeling the plasma membrane. These
processes occur continually in most eukaryotic cells, yet

A

the
amount of plasma membrane in a nongrowing cell remains
fairly constant. The addition of membrane by one process
appears to offset the loss of membrane by the other.

48
Q

cells acquire

A

chemical energy to do the

work of life.