Lecture Cell Chapters 5 and 6 Biological Membranes and Cell Communication.

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Lecture Cell Chapters 5 and 6 Biological Membranes and Cell Communication

Transcript of Lecture Cell Chapters 5 and 6 Biological Membranes and Cell Communication.

Page 1: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Lecture Cell

Chapters 5 and 6 Biological Membranes and

Cell Communication

Page 2: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Membrane structure, I

Selective permeability Amphipathic~

hydrophobic & hydrophilic regions

Singer-Nicolson: fluid mosaic model

Page 3: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Fig. 5-6, p. 111

Glycoprotein

Glycolipid

Cytosol

Hydrophilic

Carbohydratechain

Hydrophilic

HydrophobicExtracellular fluid

Cholesterol

α-helix Integralproteins

Peripheralprotein

Carbohydratechains

Page 4: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Membrane structure, II

Phospholipids~ membrane fluidity Cholesterol~ membrane stabilization “Mosaic” Structure~ Integral proteins~ transmembrane

proteins Peripheral proteins~ surface of

membrane Membrane carbohydrates ~ cell to

cell recognition; oligosaccharides (cell markers); glycolipids; glycoproteins

Page 5: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Fig. 5-2b, p. 108

Integral(transmembrane)

protein

(b) Fluid mosaic model. According to this model, a cellmembrane is a fluid lipid bilayer with a constantly changing“mosaic pattern“ of associated proteins.

Phospholipidbilayer

Peripheralprotein

Hydrophilicregion of protein

Hydrophobicregion of protein

Page 6: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

The Lipid Bilayer

Lipids of the bilayer fluid or liquid-crystalline state

Proteins move within the membrane

Page 7: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Membrane Proteins

Page 8: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Functions of Membrane Proteins

Page 9: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Membrane traffic Diffusion~ tendency of any

molecule to spread out into available space

Concentration gradient Passive transport~ diffusion

of a substance across a biological membrane without using energy

Osmosis~ the diffusion of water across a selectively permeable membrane

Page 10: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Diffusion

Page 11: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Osmosis

Page 12: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Fig. 5-12, p. 117

Pressure appliedto piston to resistupward movement

Watermolecule

Selectivelypermeablemembrane

Pure water

Moleculeof solute

Waterplussolute

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Water balance Osmoregulation~ control

of water balance

Hypertonic~ higher concentration of solutes

Hypotonic~ lower concentration of solutes

Isotonic~ equal concentrations of solutes

Cells with Walls: Turgid (very firm)

Flaccid (limp)

Plasmolysis~ plasma membrane pulls away from cell wall

Page 14: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Osmotic Pressure

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Fig. 5-13a, p. 118

SolutemoleculesNo net water

movement

(a) Isotonic solution.When a cell is placed in anisotonic solution, watermolecules pass in and outof the cell, but the netmovement of watermolecules is zero.

Outsidecell

Insidecell

H20molecules

Page 16: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Fig. 5-13b, p. 118

Outsidecell

(b) Hypertonic solution.When a cell is placed in ahypertonic solution, thereis a net movement ofwater molecules out of thecell (blue arrow). The cellbecomes dehydrated andshrunken.

Net water movementout of the cell

Insidecell

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Fig. 5-13c, p. 118

10 μ

m

(c) Hypotonic solution.When a cell is placed in ahypotonic solution, the netmovement of watermolecules into the cell(blue arrow) causes the cellto swell or even burst.

Insidecell

Outsidecell

Net water movementinto the cell

Page 18: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Turgor and Plasmolysis

Page 19: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Fig. 5-14, p. 119

Plasmamembrane

Vacuole

Vacuolarmembrane(tonoplast)

Vacuole

Cytoplasm

Plasmamembrane Nucleus

Page 20: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Specialized Transport

Transport proteins Facilitated diffusion~

passage of molecules and ions with transport proteins across a membrane down the concentration gradient

Active transport~ movement of a substance against its concentration gradient with the help of cellular energy

Page 21: Lecture Cell  Chapters 5 and 6 Biological Membranes and  Cell Communication.

Facilitated Diffusion

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Fig. 5-16a, p. 120

1 Glucose binds to GLUT 1.

Cytosol

Lowconcentrationof glucose

Glucosetransporter(GLUT 1)

Highconcentrationof glucose

Glucose

Outside cell

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Fig. 5-16b, p. 120

GLUT 1 changes shape andglucose is released inside cell.

2

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Fig. 5-16c, p. 120

GLUT 1 returns to its originalshape.

3

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Types of Active Transport Sodium-potassium pump Exocytosis~ secretion of

macromolecules by the fusion of vesicles with the plasma membrane

Endocytosis~ import of macromolecules by forming new

vesicles with the plasma membrane

•phagocytosis•pinocytosis•receptor-mediated endocytosis (ligands)

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Fig. 5-17a, p. 121

(a) The sodium–potassium pump is a carrier protein that requiresenergy from ATP. In each complete pumping cycle, the energy ofone molecule of ATP is used to export three sodium ions (Na+)and import two potassium ions (K+).

So

diu

mco

nce

ntr

atio

n g

rad

ien

t

Lower

Higher

Cytosol

Outsidecell

Activetransportchannel

Lower

Higher

Po

tass

ium

c on

c en

trat

ion

gr a

die

nt

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Fig. 5-17b, p. 121

1. Three Na+ bindto transport protein.

2. Phosphate group istransferred from ATPto transport protein.

3. Phosphorylationcauses carrier proteinto change shape, releasing3 Na+ outside cell.

4. Two K+ bind totransport protein.

5. Phosphate is released.6. Phosphate release causescarrier protein to returnto its original shape. TwoK+ ions are released insidecell.

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Phagocytosis

Large particles enter cell

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Receptor-MediatedEndocytosis

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Intracellular junctions PLANTS: Plasmodesmata: cell wall

perforations; water and solute passage in plants

ANIMALS: Tight junctions~ fusion of

neighboring cells; prevents leakage between cells

Desmosomes~ riveted, anchoring junction; strong sheets of cells

Gap junctions~ cytoplasmic channels; allows passage of materials or current between cells

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Tight Junctions

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Gap Junctions

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Cell Signaling

1. Synthesis, release, transport of signaling molecules

- neurotransmitters, hormones, etc- ligand binds to a specific receptor

2. Reception of information by target cells

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Cell Signaling

3. Signal transduction- receptor converts extracellular signal into

intracellular signal- causes change in the cell

4. Response by the cell

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Cell Signaling

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Fig. 6-2, p. 136

Signalingprotein

Protein thatregulates a gene

Alteredgene activity

EnzymeProtein

Alteredmembrane

permeability

Alteredmetabolism

Response

Signaltransduction

Cell sendssignal

Reception

Receptor

Signalingmolecules

1

2

3

4

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Local Regulators

Paracrine regulation diffuse through interstitial fluid act on nearby cells

Local regulators histamine growth factors prostaglandins nitric oxide

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Local Signals

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Neurotransmitters

Chemical signals released by neurons (nerve cells)

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Hormones

Chemical messengers in plants and animals

Secreted by endocrine glands in animals

Transported by blood to target cells

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Hormones