Exam 4 - Lecture 8 Flashcards

1
Q

Membranes define

A

the boundaries of a cell and its internal
compartments

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2
Q

The 5 Functions of Membranes

A
  1. Define boundaries of a cell and organelles and act as
    permeability barriers
  2. Serve as sites for biological functions, such as electron
    transport
  3. Possess transport proteins that regulate the movement of
    substances into and out of cells and organelles
  4. Contain protein molecules that act as receptors to detect
    external signals
  5. Provide mechanisms for cell-to-cell contact, adhesion,
    and communication
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3
Q

Membranes are effective permeability barriers because

A

their interior is hydrophobic

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4
Q

what surrounds the whole cell?

A

the plasma membrane

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5
Q

intracellular membranes do what

A

compartmentalize functions within the cell

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6
Q

Membranes are associated with specific functions
because

A

the molecules responsible for the functions are embedded in or localized on membranes

The specific enzymes associated with particular
membranes can be used to characterize a specific
membrane

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7
Q

Membrane Proteins Regulate

A

the transport of solutes

Membrane proteins carry out and regulate the
transport of substances across the membrane

Cells and organelles take up nutrients, ions, gases,
water, and other substances, and they expel
products and wastes

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8
Q

what are the two ways substances can move into or out of the cell

A

Some substances diffuse directly across
membranes, whereas others must be moved by
specific transporters

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9
Q

Membrane Proteins Detect and Transmit

A

Electrical and Chemical Signals

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10
Q

A cell receives information from its environment as

A

electrical or chemical signals at its surface

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11
Q

Signal transduction describes the mechanisms by which

A

signals are transmitted from the outer
surface to the interior of a cell

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12
Q

Chemical signal molecules usually bind to

A

membrane proteins, known as receptors, on the
outer surface of the plasma membrane

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13
Q

describe signal transduction

A

Binding of signal molecules to their receptors
triggers chemical events on the inner membrane
surface that ultimately lead to changes in cell
function
 Membrane receptors allow cells to recognize,
transmit, and respond to a variety of specific
signals in nearly all types of cells

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14
Q

Membrane Proteins Mediate

A

Cell Adhesion
and Cell-to-Cell Communication

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15
Q

Cell-to-cell contacts, critical in animal development,
are often mediated by

A

cadherins

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16
Q

cadherins

A

mediate cell to cell contact
Cadherins have extracellular sequences of amino
acids that bind calcium and promote adhesion
between similar types of cells in a tissue

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17
Q

4 types of junctions

A

adhesive junctions
tight junctions
gap junctions
plasmodesmata

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18
Q

what do Adhesive junctions do

A

hold cells together

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19
Q

Tight junctions form

A

seals that block the passage of
fluids between cells

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20
Q

Gap junctions allow for

A

communication between
adjacent animal cells

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21
Q

plasmodesmata are present in

A

plants

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22
Q

describe the fluid mosaic model

A

The model envisions a membrane as two fluid
layers of lipids with proteins within and on the
layers

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23
Q

Overton and Langmuir

A

Lipids Are Important
Components of Membranes

Overton: cell surface had some kind
of lipid “coat” on it
 Langmuir: phospholipids
areamphipathic

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24
Q

Gorter and Grendel:

A

The Basis of Membrane
Structure Is a Lipid Bilayer

Structure is a lipid bilayer, with the
nonpolar regions of the lipids facing
inward

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25
Davson and Danielli: Membranes Also Contain
Proteins
26
go look at the research
did not make flashcards
27
Electron microscopy revealed that
there was not enough space on either side of the bilayer for an additional layer of protein ( not ssure of in new slides)
28
The Davson–Danielli model also did not account for
not in updated slides
29
Membranes are susceptible to digestion by
phospholipases, suggesting that membrane lipids are exposed ( not sure if in new slides)
30
Scientists were unable to isolate “surface” proteins from membranes unless
organic solvents or detergents were used
31
The fluid mosaic bilayer model accounts
or all the inconsistencies with previous models
32
the fluid mosaic model has two key features
A fluid lipid bilayer  A mosaic of proteins attached to or embedded in the bilayer
33
Transmembrane Segments
Most Membrane Proteins Contain Transmembrane Segments  Most integral membrane proteins have one or more hydrophobic segments that span the lipid bilayer  These transmembrane segments anchor the protein to the membrane
34
the first membrane protein shown to possess this structural feature
was Bacteriorhodopsin
35
How are membranes ordered and are the homogenous or heterogenous?
Not homogenous, freely mixing structures  Ordered through dynamic microdomains called lipid rafts
36
Most cellular processes that involve membranes depend on
structural complexes of specific lipids and proteins
37
Membrane lipids are important components of the “fluid” part of the fluid mosaic model  Membranes contain several types of lipids what are the main classes of lipids
phospholipids, glycolipids, and sterols
38
most abundant lipids in membranes
phospholipids
39
what are the two different bases for phospholipids?
glycerol-based phosphoglycerides and the sphingosine-based sphingolipids
40
Glycolipids are formed by the addition of
carbohydrates to lipids
41
what are two variations of glycerol
Some are glycerol based (the glycoglycerolipids), and some are sphingosine based (the glycosphingolipids)
42
The most common glycosphingolipids are
cerebrosides and gangliosides
43
Cerebrosides are
are neutral glycolipids; each molecule has an uncharged sugar as its head group
44
A ganglioside has
an oligosaccharide head group with one or more negatively charged sialic acid residues
45
Cerebrosides and gangliosides are especially prominent
in brain and nerve cells
46
The membranes of most eukaryotes contain significant amounts of
sterols
47
The main sterol in animal cell membranes is
cholesterol
48
cholesterol function
needed to stabilize and maintain membranes
49
Plant cell membranes contain what type of sterol?
phytosterols
50
fungal cell membranes contain
ergosterol, similar to cholesterol
51
Fatty acids are components of all membrane lipids except
the sterols
52
the long hydrocarbon tails provide as a
barrier to diffusion of polar solutes
53
The sizes of membrane fatty acids range between
12 and 20 carbons long, which is optimal for bilayer formation and dictates the usual thickness of membranes (6–8 nm)
54
Fatty Acids Vary in Degree of
saturation
55
Palmitate has
16 carbons
56
stearate has how many carbons
18 carbons
57
palmitate and stearate are common
saturated fatty acids
58
Oleate has how many double bonds
one double bond
59
linoleate has how many double bonds
two double bonds
60
Oleate (one double bond) and linoleate (two double bonds) are both
18-carbon unsaturated fatty acids
61
Polyunsaturated fatty acids have more than one
double bond
62
Omega-3 fatty acids are
polyunsaturated fatty acids that are essential for normal human development
63
Omega-3 fatty acids may also reduce the risk of
heart disease
64
Lipids can be isolated, separated, and studied using
nonpolar solvents such as acetone and chloroform
65
Thin-layer chromatography (TLC) is used to
separate different kinds of lipids based on their relative polarities
66
the bottom of the TLC plate is called the
origin
67
A nonpolar organic solvent moves up the plate by
capillary action taking different lipids with it to varying degrees
68
Nonpolar lipids have little affinity for
silicic acid on the plate, so they move readily with the solvent, near the solvent front
69
in reference to TLC Polar lipids will interact variably (depending on how polar they are) with
the silicic acid, and their movement will be slowed proportionately
70
Membrane asymmetry describes the difference in degree of what component?
is the difference between the monolayers regarding the kind of lipids present and the degree of saturation of fatty acids in the phospholipids
71
Most of the glycolipids in the plasma membrane of animal cells are in what layer
outer layer
72
Membrane asymmetry is established during
the synthesis of the membrane
73
does membrane asymmetry change?
Once established, membrane asymmetry does not change much
74
transverse diffusion
The movement of lipids from one monolayer to another requires their hydrophilic heads to move all the way through the hydrophobic interior of the bilayer This transverse diffusion (or “flip-flop”) is relatively rare
75
describe lipid mobility
Lipids Move Freely Within Their Monolayer Lipids are mobile within their monolayer Movements are rapid and random
76
types of lipids motion
Rotation - Rotation of phospholipids about their axes can occur lateral diffusion - Phospholipids can also move within the monolayer, via lateral diffusion
77
which membranes tend to have transverse diffusion / flip-flop?
Some membranes, in particular the smooth ER membrane
78
why are some membranes prone to transverse diffusion? what is the substance called?
because they have proteins that catalyze the flip-flop of membrane lipids  These proteins are called phospholipid translocators, or flippases
79
proteins catalyze the lip flop
phospholipid translocators, or flippases
80
The lipid bilayer behaves as a fluid that permits the movement of both
lipids and Proteins
81
How far can lipids move
Lipids can move as much as several μm per second within the monolayer
82
Lateral diffusion can be demonstrated using what method
Fluorescence recovery after photobleaching (FRAP)
83
FRAP measures lipid ______
mobility
84
how does FRAP work
Investigators label lipid molecules in a membrane with a fluorescent dye.  A laser beam is used to bleach the dye in a small area, creating a dark spot on the membrane.  The membrane is observed afterward to determine how long it takes for the dark spot to disappear, a measure of how quickly new fluorescent lipids move in
85
Membranes Function Properly Only in the________ state
Fluid
86
what affects membrane fluidity
Membrane fluidity changes with temperature, decreasing as temperature falls and vice versa
87
what is the transition temperature?
a characteristic of every lipid bilayer- the transition temperature Tm, the temperature at which it becomes fluid The Tm is the point of maximum heat absorption as the membrane changes from the gel to the fluid state
88
change is state of the membrane is called
Phase transition ( solid to liquid)
89
what happens to memrane functions when the temp is below Tm ?
Below the Tm , any functions that rely on membrane fluidity will be disrupted
89
The transition temperature can be measured by
differential scanning calorimetry - The membrane is placed inside a calorimeter, and the uptake of heat is measured as temperature is increased
90
Fluidity of a membrane depends mainly on
that fatty acids that it contains
91
what two characteristics about fatty acids affect membrane fluidity
The length of fatty acid chains and the degree of saturation both affect the fluidity of the membrane
92
what has a higher Tm? Long chains and saturated fats or short chains and unsaturated?
Long-chain and saturated fatty acids have higher Tm values, whereas short-chain and unsaturated fatty acids have lower Tm values
93
how do saturated farts sit together in the membrane
they pack well together in the membrane ( linear)
94
how do double bonds affect fatty acid shape
Fatty acids with one or more double bonds have bends in the chains that prevent them from packing together neatly
95
which is more fluid saturated or unsaturated
Because saturated bonds pack together and unsaturated bonds have a bend - -- unsaturated fatty acids are more fluid than saturated fatty acids and have lower Tm values
96
Why do Most plasma membrane fatty acids vary in chain length and degree of saturation?
to ensure that membranes are fluid at physiological temperatures
97
what type of double bonds do unsaturated fatty acids typically have ? and what type of bonds do trans fats normally have?
Most unsaturated fatty acids have cis double bonds commercially produced trans fats, which pack together like saturated fats do
98
how do sterols impact membrane fluidity ?
The intercalation of rigid cholesterol molecules into a membrane decreases its fluidity and increases the Tm However, cholesterol also prevents hydrocarbon chains of phospholipids from packing together tightly and so reduces the tendency of membranes to gel upon cooling  Therefore, cholesterol is a fluidity buffer; sterols in other organisms may function similarly Other Effects of Sterols on Membranes  Sterols decrease the permeability of membranes to ions and small polar molecules  This is likely because they fill spaces between the hydrocarbon chains of phospholipids  This effectively blocks the routes that ions and small molecules would take through the membran
99
cholesterol's impact on the membrane gives it the name....
fluidity buffer
100
how do sterols affect permeability of membranes to ions and small polar molecules??? Explain why
Sterols decrease the permeability of membranes to ions and small polar molecules  This is likely because they fill spaces between the hydrocarbon chains of phospholipids  This effectively blocks the routes that ions and small molecules would take through the membrane
101
How do organisms regulate membrane fluidity?
Most organisms can regulate membrane fluidity by varying the lipid composition of the membranes
102
poikilotherms
organisms that cannot regulate their body temperature use homeoviscous adaptation, compensating for changes in temperature by altering the length and degree of saturation of fatty acids in their membranes
103
desaturase enzyme
Some organisms have a desaturase enzyme, which introduces double bonds into fatty acids as needed
104
In plants and yeasts, temperature-related fluidity changes are tied to
the increased solubility of oxygen at lower temperatures More oxygen is available at low temperatures, and oxygen acts as a substrate for desaturase, allowing membrane fluidity to be maintained at lower temperatures
104
Lipid Rafts Are
Localized Regions of Membrane Lipids That Are Involved in Cell Signaling they are associated with specific proteins they are also called lipid microdomains These are dynamic structures, changing composition as lipids and proteins move into and out of them
105
how do lipid rafts in the outer membrane compare to those in the rest of the membrane?.
Lipid rafts in the outer monolayer of animal cells have elevated levels of cholesterol and glycosphingolipids and are less fluid than the rest of the membrane
106
Lipid Raft Formation
Early models of raft formation proposed that localized regions of tightly associated cholesterol and glycosphingolipid molecules attracted particular proteins to them  Raft-associated proteins sometimes are lipoproteins, with fatty acids attached to them  Some of the more than 200 known raft-associated proteins capture and organize particular lipid rafts  Lipid rafts contain actin-binding proteins, suggesting that the cytoskeleton may play a role in their formation and organization
107
Functions of Lipid Rafts
Lipid rafts are thought to have roles in detecting and responding to exracellular signals  For example, lipid rafts have roles in  Transporting nutrients and ions across membranes  Binding activated immune system cells to their microbial targets  Transporting cholera toxin into intestinal cells
108
Receptors in Lipid Rafts
When a receptor molecule on the outer surface of the plasma binds its ligand, it can move into lipid rafts also located in the outer monolayer Lipid rafts containing receptors are coupled to lipid rafts on the inner monolayer Some lipid rafts contain kinases, enzymes that generate second messengers in a cell via phosporylation of target molecules
109
Some lipid rafts contain kinases which are
enzymes that generate second messengers in a cell via phosporylation of target molecules
110
what is the main component of the "mosaic" part of the mebrane
The mosaic part of the fluid mosaic model includes lipid rafts and other lipid domains  However, membrane proteins are the main components
111
Support for the fluid mosaic model came from studies involving
freeze fracturing - a bilayer or membrane is frozen and then hit sharply with a diamond knife  The resulting fracture often follows the plane between the two layers of membrane lipid
112
Freeze-Fracture Analysis of Membranes (fix)
When a fracture plane splits a membrane into its two layers, particles the size and shape of globular proteins can be seen  The E surface is the exoplasmic face, and the P surface is the protoplasmic face  The protein/lipid ratio varies among cell types
113
Membrane proteins fall into three categories:
Integral, peripheral, and lipid anchored
114
Membrane proteins have different _________ and so occupy different positions in or on membranes
hydrophobicites ^ which determines how easily such proteins can be extracted from membranes
115
Integral membrane proteins
are embedded in the lipid bilayer because of their hydrophobic regions
116
Lipid-anchored proteins are
hydrophilic and attached to the bilayer by covalent attachments to lipid molecules embedded in the bilayer
116
Peripheral proteins are
hydrophilic and located on the surface of the bilayer
117
Integral Membrane Proteins in depth (fix)
Most membrane proteins possess one or more hydrophobic regions with an affinity for the interior of the lipid bilayer  These are integral membrane proteins, with hydrophobic regions embedded in the interior membrane bilayer  They are difficult to remove from membranes by standard isolation procedures  Some integral membrane proteins, called integral monotropic proteins, are embedded in just one side of the bilayer  However, most are transmembrane proteins that span the membrane and protrude on both sides  Transmembrane proteins cross either once (singlepass proteins) or several times (multipass proteins)
118
Most transmembrane proteins are anchored to the lipid bilayer by one or more hydrophobic
Transmembrane segments
119
conformation and length of transmembrane segments
the polypeptide chain appears to span the membrane in an α-helical conformation about 20–30 amino acids long  Some are arranged as a closed β sheet called a β barrel
120
Singlepass membrane proteins have the______ terminus extending from one surface of the membrane and the ________ from the other
Singlepass membrane proteins have the C-terminus extending from one surface of the membrane and the N-terminus from the other  For example, glycophorin is a singlepass protein on the erythrocyte plasma membrane that is oriented so the C-terminus is on the inner surface and the N-terminus is on the outer
121
describe Multipass Membrane Proteins
Multipass membrane proteins have 2–20 (or more) transmembrane segments  For example, bacteriorhodopsin has seven transmembrane segments positioned to form a channel
122
Membrane proteins that lack discrete hydrophobic regions do not penetrate the lipid bilayer are called
peripheral membranes
123
peripheral membranes lack what ?
discrete hydrophobic regions do not penetrate the lipid bilayer
124
peripheral membrane proteins are bound to membrane surfaces through
weak electrostatic forces and hydrogen bonds Some hydrophobic residues play a role in anchoring them to the membrane surface
125
The polypeptide chains of lipid-anchored membrane proteins are located on the
surfaces of membranes They are covalently bound to lipid molecules embedded in the bilayer  Proteins bound to the inner surface of the plasma membrane are linked to fatty acids, or isoprenyl groups
126
Types of Lipid-Anchored Membrane Proteins
Fatty acid-anchored membrane proteins Isoprenylated membrane proteins GPI-anchored membrane proteins
126
Fatty acid-anchored membrane proteins
are attached to a saturated fatty acid, usually myristic acid (14C) or palmitic acid (16C)
127
Isoprenylated membrane proteins are synthesized in the
cytosol and then modified by addition of multiple isoprenyl groups (5C) usually farnesyl (15C) or geranylgeranyl (20C) groups
128
GPI-anchored membrane proteins are _________ linked to __________
are covalently linked to glycosylphosphatidylinositol
129
Isolation of Membrane Proteins
Peripheral membrane proteins are usually easy to isolate by altering pH or ionic strength  Chelating (cation-binding) agents are also used to solubilize peripheral membrane proteins  Lipid-anchored proteins are isolated by similar means
130
Isolating Integral Membrane Proteins
Integral membrane proteins are difficult to isolate from membranes  Often detergents are used that disrupt hydrophobic interactions and dissolve the lipid bilayer
131
Electrophoresis is a
group of techniques that use an electric field to separate charged molecules  How quickly a molecule moves during electrophoresis depends on both charge and size  Electrophoresis uses various support media, most commonly polyacrylamide or agarose
131
How does Electrophoresis of Membrane Proteins work?
 Membrane fragments are solubilized in sodium dodecyl sulfate (SDS), which disrupts protein- protein and protein-lipid associations  The proteins are thus coated with negatively charged detergent molecules  The proteins are loaded onto a polyacrylamide gel and an electrical potential is applied
132
 Two-dimensional SDS-polyacrylamide gel electrophoresis (SDS-PAGE) separates....  Following electrophoresis, polypeptides can be identified by
 Two-dimensional SDS-polyacrylamide gel electrophoresis (SDS-PAGE) separates proteins in two dimensions, first by charge and then by size  Following electrophoresis, polypeptides can be identified by Western blotting  In this technique, proteins are transferred to a membrane and bound by specific antibodies
133
Some integral membrane proteins, called integral monotropic proteins, are embedded
in just one side of the bilayer  However, most are transmembrane proteins that span the membrane and protrude on both sides
133
Affinity labeling
utilizes radioactive molecules that bind to certain proteins based on function For example, cytochalasin B is an inhibitor of glucose transport
134
membrane reconstitution
proteins are extracted from membranes and separated individually
134
Membranes exposed to radioactive cytochalasin B will likely have
the radioactivity bound to proteins involved in glucose transport
135
purified proteins
are mixed with phospholipids to form vesicles call liposomes
135
Liposomes can be loaded with
particular molecules and tested for their ability to carry out certain functions
136
X-ray crystallography
an be used to determine the structure of proteins that can be isolated in crystalline form  Membrane proteins are hard to isolate and crystallize
137
X-ray crystallography is widely used to determine
three-dimensional structure of proteins
137
An alternative approach to X-ray crystallography
hydropathy analysis
138
Integral membrane proteins are difficult or easy to isolate and crystallize
difficult
139
hydropathy (or hydrophobicity) plot
the number and location of transmembrane segments in a membrane protein can be inferred if the protein sequence is known A computer program identifies clusters of hydrophobic residues, calculating a hydropathy index for successive “windows” along the protein
139
Site-specific mutagenesis allows determination of
how certain amino acids affect protein function
140
hydropathy (or hydrophobicity) plot is used for
The number and location of transmembrane segments in a membrane protein can be inferred if the protein sequence is known
140
hydropathy index
calculating hydrophobic residues
141
protein sequence is hard to determine unlike DNA bc
different amino acids are encoded with different codes. Histodine has 6 codes so you have to know which code was responsible
142
Membrane Proteins Are Oriented
Asymmetrically Across the Lipid Bilayer
143
Site-specific mutagenesis
allows determination of how certain amino acids affect protein function
144
Once in place, in or on one of the monolayers, proteins ( can or cannot) move across the membrane from one surface to the other
proteins cannot move across the membrane from one surface to the other  All the molecules of a particular protein are oriented the same way in the membrane
145
The enzyme lactoperoxidase (LP) can be used to The enzyme galactose oxidase (GO) can be used to
attach (125^I) to proteins label carbohydrate side chains attached to membrane proteins and lipids
145
Radioactive labeling procedures are used to
distinguish between proteins on inner and outer surfaces of membrane vesicles
146
Glycoproteins
are membrane proteins with carbohydrate chains covalently linked to amino acid side chains ( covalent = strong)
146
The PROCESS of adding a carbohydrate side chain to a protein is called
glycosylation
147
glycosylation
The addition of a carbohydrate side chain to a protein
148
where does Glycosylation occurs ?
ER and Golgi compartments
149
Glycosylation involves linkage of the carbohydrate to
The nitrogen atom of an amino group or The oxygen atom of a hydroxl group
150
N-linked glycosylation
Glycosylation involves linkage of the carbohydrate to The nitrogen atom of an amino group (N-linked glycosylation) of an asparagine residue
151
O-linked glycosylation
Glycosylation involves linkage of the carbohydrate to The oxygen atom of a hydroxl group (O-linked glycosylation) of a serine, threonine, or modified lysine or proline residue
152
explain the statement : Membrane Proteins Vary in Their Mobility
Membrane proteins are more variable than lipids in their ability to move freely within the membrane  Some proteins can move freely, whereas others are constrained because they are anchored to protein complexes
153
Experimental Evidence for Protein Mobility
Evidence for mobility of some membrane proteins comes from cell fusion experiments  These experiments were performed by David Frye and Michael Edidin
154
The Frye and Edidin Experiments
Frye and Edidin fused human and mouse cells and used two fluorescent antibodies, each with a differently colored dye linked to it  The anti-mouse antibodies were linked to fluorescein, a green dye; and the anti-human antibodies were linked to rhodamine, a red dye  Within a few minutes of fusion, the red and green region proteins began to intermix
155
Protein distribution on memnbranes are different
image on slide 25 When plasma membranes are examined in freeze-fracture micrographs, the embedded proteins appear to be randomly distributed  The same is true for other types of membranes
156
Overcoming the permeability barrier of cell membranes is crucial to proper functioning of the cell. What does this mean inte rms on the transports in and out?
Specific molecules and ions need to be selectively moved into and out of the cell or organelle
157
Membranes are protective barriers described as
selectively permeable or semipermeable
158
Homeostasis
Cells and cellular compartments are able to accumulate a variety of substances in concentrations that are very different from those of the surroundings
159
solutes
Most of the substances that move across membranes are dissolved gases, ions, and small organic molecules
160
A central aspect of cell function is selective
transport
161
Three quite different mechanisms are involved in moving solutes across membranes:
Simple Diffusion, Facilitated Diffusion, Active Transport
162
intrinsic directionality
opposite direction requirers active transport?
163
The movement of a molecule that has no net charge is determined by its
concentration gradient
164
Simple diffusion and facilitated diffusion involves (ender or exergonic?) movement
exergonic movement “down” the concentration gradient (negative ΔG)
165
Active transport involves ( ender or exergonic) movement
endergonic movement “up” the concentration gradient (positive ΔG)
166
The movement of an ion is determined by its
electrochemical potential
167
electrochemical potential
the combined effect of its concentration gradient and the charge gradient across the membrane
168
The active transport of ions across a membrane creates a
charge gradient, or membrane potential (Vm), across the membrane
169
Simple Diffusion
Unassisted Movement Down the Gradient
170
the unassisted net movement of a solute from
high to lower concentration
171
Simple Diffusionis only possible for...
gases, nonpolar molecules, or small polar molecules such as water, glycerol, or ethanol
172
Diffusion always moves solutes toward
equilibrium: solutes will move toward regions of lower concentration until the concentrations are equal
173
Osmosis Is
the Diffusion of Water Across a Selectively Permeable Membrane
174
Water molecules, being uncharged are not affected by
the membrane potential
175
Water concentration is not
appreciably different on opposite sides of a membrane
176
Osmosis: water will move toward the region of
higher solute concentration
177
If the solute concentration is higher outside the cell, the SOLUTION is called
hypertonic
177
Osmolarity
Is the total solute concentrations inside versus outside of the cel
178
hypotonic in plants is called ( see figure and know differnet names)
turgid
178
If the solute concentration is lower outside the cell, the solution is called
hypotonic
179
isotonic solution
solute concentration inside and outside the cell is the same
179
Animal cells vs cells with cell walls (plants, algae, fungi, and many bacteria )
act differently
180
Facilitated Diffusion:
Protein-Mediated Movement Down the Gradient
180
Most substances in the cell are too large or too polar to cross membranes by simple diffusion  These can move in and out of cells only with the assistance of
Transport proteins
181
movment using transport protein is ( exergonic or endetgonic)
This process is exergonic: the solute diffuses as dictated by its concentration gradient
182
The role of the transport proteins is just to provide
a path through the lipid bilayer, allowing the “downhill” movement of a polar or charged solute
182
Carrier proteins aka
transporters or permeases
183
Carrier proteins bind
bind solute molecules on one side of a membrane, undergo a conformation change, and release the solute on the other side of the membrane
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Channel proteins form
form hydrophilic channels through the membrane to provide a passage route for solutes
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The alternating conformation model states that
a carrier protein is allosteric protein and alternates between two conformational states
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Carrier Proteins Alternate Between
Two Conformational States
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what are the two conformational states
n one state, the solute-binding site of the protein is accessible on one side of the membrane  The protein shifts to the alternate conformation, with the solute-binding site on the other side of the membrane, triggering solute release
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Carrier Proteins Are Analogous to Enzymes in Their
Specificity and Kinetics
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Facilitated diffusion involves binding
a substrate on a specific solute-binding site
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The carrier protein and solute form an
intermediate
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After conformational change, the “product” is
released (the transported solute)
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Carrier proteins are regulated by
external factors
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Carrier Proteins Transport how many solutes
1-2 solutes
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When a carrier protein transports a single solute across the membrane, the process is called
uniport
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uniport
When a carrier protein transports a single solute across the membrane
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A carrier protein that transports a single solute is called a
uniporter
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uniporter
A carrier protein that transports a single solute
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When two solutes are transported simultaneously, and their transport is coupled, the process is called
coupled transport
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coupled transport
When two solutes are transported simultaneously, and their transport is coupled
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symport (or cotransport)
If the two solutes are moved across a membrane in the same direction
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If the two solutes are moved across a membrane in the same direction, the process is referred to as
symport (or cotransport)
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antiport (or countertransport)
the solutes are moved in opposite directions,
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If the solutes are moved in opposite directions, the process is called
antiport (or countertransport)
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Transporters that mediate these ( symport and antiport) processes are
symporters and antiporters
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pores
large and nonspecific channels on the outer membranes of bacteria, mitochondria, and chloroplasts
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Pores are formed by
transmembrane proteins called porins that allow passage of solutes up to a certain molecular weight to pass
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Most channels are
smaller and highly selective
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Most of the smaller channels are involved in
ion transport and are called ion channels
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ion channels are involved in
involved in ion transport
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The movement of solutes through ion channels is much ( faster OR SLOWER) than transport by carrier proteins
faster because conformation changes are not required
210
There are three types of channels: ???
ion channels, porins, and aquaporins
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Channel Proteins Facilitate Diffusion by Forming
Hydrophilic Transmembrane Channels
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Ion Channels
transmembrane proteins that allow rapid passage of specific ions typically gated meaning they open and close in response to some stimulus
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Voltage-gated channels
open and close in response to changes in membrane potential
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Ligand-gated channels
are triggered by the binding of certain substances to the channel protein
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Mechanosensitive channels
respond to mechanical forces acting on the membrane
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porins:
transmembrane proteins that allow rapid passage of various solutes
216
the transmembrane segments of porins cross the membrane as
β barrels
217
Polar side chains line the inside of the pore, allowing passage of
many hydrophilic solutes
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The outside of the barrel contains many
nonpolar side chains that interact with the hydrophobic interior of the membrane
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Aquaporins (AQPs)
transmembrane channels that allow rapid passage of water
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All aquaporins are
tetrameric integral membrane proteins The identical monomers associate with their 24 transmembrane segments oriented to form four central channels  The channels, lined with hydrophilic side chains, are just large enough for water molecules to pass through one at a time
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active transport moves what direction on a gradient
protein-mediated movement up the gradient
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Active transport is used to move
solutes up a concentration gradient, away from equilibrium
222
Active transport couples
endergonic transport to an exergonic process, usually ATP hydrolysis
223
Active transport performs three important cellular functions
1. Uptake of essential nutrients 2. Removal of wastes 3. Maintenance of nonequilibrium concentrations of certain ions
224
Active Transport Is
Unidirectional
225
Active transport differs from diffusion (both simple and facilitated) in
the direction of transport  Diffusion is nondirectional with respect to the membrane and proceeds as directed by the concentrations of the transported substances  Active transport has an intrinsic directionality
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The Coupling of Active Transport to an Energy Source May Be
Direct or Indirect
227
describe direct active transport (reference slide)
(primary active transport), the accumulation of solute molecules on one side of the membrane is coupled directly to an exergonic chemical reaction  This is usually hydrolysis of ATP  Transport proteins driven by ATP hydrolysis are called transport ATPases or ATPase pumps
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Indirect active transport
depends on the simultaneous transport of two solutes Favorable movement of one solute down its gradient drives the unfavorable movement of the other up its gradient  This can be a symport or an antiport, depending on whether the two molecules are transported in the same or different directions
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