chap. 8 membrane structure and function a.p.biology mr. orndorff october 2005

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Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

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Page 1: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Chap. 8 Membrane Structure and Function

A.P.Biology

Mr. Orndorff

October 2005

Page 2: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Molecular models of membranes

• Overton (1895): membranes made of lipids because lipid soluble substances pass through membranes more rapidly.

• Gorton and Grendel (1925): membranes are phospholipid bilayers—measured amount of phospholipids in red blood cells enough to cover cells with two layers.

Page 3: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Amphipathic molecules (Fig. 5.12)

Page 4: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Cholesterol is amphipathic (Fig. 5.14)

Page 5: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Artificial membranes(Fig. 8.1)

Page 6: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Fluidity of membranes(Fig. 8.3)

Page 7: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Two generations of membrane models (Fig. 8.2)

Davson-Danielli model (1935)

Singer-Nicolson model (1972)

Page 8: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Animal Cell’s Plasma Membrane (Fig. 8.5)

Page 9: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Structure of transmembrane protein (Fig. 8.6)

Page 10: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Evidence for drifting proteins(Fig. 8.4)

Page 11: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Functions of membrane proteins (Fig. 8.8)

Page 12: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Passive vs. active transport

• Materials move down concentration gradient

• No cell energy needed • Includes diffusion,

osmosis, and facilitated diffusion

• Materials move up concentration gradient

• Cell energy required• Includes bulk flow,

active transport, endocytosis, and exocytosis

Page 13: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Concentration gradient

0

0.2

0.4

0.6

0.8

1

1.2

0 2 4 6 8 10 12

Distance from dissolving solute (mm)

Co

nc

en

tra

tio

n (

mo

lari

ty)

Page 14: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Diffusion

• Diffusing materials must be dissolved.

• Diffusion depends on the random motion of molecules.

• Diffusion is efficient only over short distances.

• Speed of diffusion depends on steepness of concentration gradient.

Page 15: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Facilitated diffusion

• Similar to diffusion.

• Dissolved substance cannot pass directly through phospholipid bilayer.

• Integral proteins in cell membrane provide channels for facilitated diffusion.

• Number of protein channels puts upper limit on efficiency of facilitate diffusion.

Page 16: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Diffusion of solutes across membranes (Fig. 8.9)

Page 17: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Osmosis = diffusion of water across a selectively permeable membrane.

• Water moves from hypotonic solutions to hypertonic solutions.– Hypertonic solution = solution with higher

concentration of dissolved solute.– Hypotonic solution = solution with lower

concentration of dissolved solute.– Isotonic solution = solution with equal

concentration of dissolved solute.

Page 18: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Osmosis (Fig. 8.10)

Page 19: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Water balance of living cells (Fig. 8.11)

Page 20: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Differences in water potential drive water transport in plant cells.

• Water potential =

pressure potential + solute potential

• Water moves from areas of high water potential to areas of low water potential.

Page 21: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Water potential and water movement (Fig. 36.3)

Page 22: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Water relations of plant cells(Fig. 36.4)

Page 23: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

One model for facilitated diffusion (Fig. 8.13)

Page 24: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Passive vs. active transport (Fig. 8.15)

Page 25: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Sodium-potassium pump (Fig. 8.14)

Page 26: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Electrogenic pump (Fig. 8.16)

Page 27: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Cotransport (Fig. 8.17)

Page 28: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Sidedness of the plasma membrane(Fig. 8.7)

Page 29: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Types of endocytosis

• Phagocytosis = “cell eating.” White blood cells engulfing bacteria in food vacuoles.

• Pinocytosis = “cell drinking.” Maturing ovum grows as it takes in nutritive fluids from surrounding follicle cells.

• Receptor-mediated endocytosis = coated pits form vesicles when specific ligands bind to receptors on the cell surface.

Page 30: Chap. 8 Membrane Structure and Function A.P.Biology Mr. Orndorff October 2005

Functions of exocytosis

• Secretion of macromolecules from cell.– Glandular secretions– Neuron signal molecules– Plant cell wall formation

• Addition of new phospholipid molecules to plasma membrane for growth.

• Addition of new integral proteins to plasma membrane for specific function.