2. 1. Membrane Organization and the Plasma Membrane 1a. The lipid bilayer

3. CYTOPLASM One layer faces the cytoplasm = cytoplasmic layer (or leaflet) The other faces either an organelle lumen or the extracellular matrix = non-cytoplasmic layer

4. Membrane Lipids: Major lipids are phospholipids and cholesterol Minor lipids are inositol phospholipids and glycolipids

5. Phospholipids are amphipathic Example: Phosphatidylcholine PHOSPHOLIPID STRUCTURE

6. PHOSPHOLIPID BEHAVIOR -Can flex, rotate, and are laterally mobile within a leaflet (with regional restrictions) -Spontaneous flipping between leaflets rare -Enzymes (flippases) can flip phospholipids between leaflets

7. Major Phospholipids (4) ER - evenly distributed between leaflets; plasma membrane - choline-containing phospholipids (PC & SM) - in non-cytosolic leaflet; amino phospholipids (PE & PS) - in cytosolic leaflet Exhibit a change in organization from ER to plasma membrane

8. Cholesterol; a major membrane lipid

9. Minor membrane lipids Inositol phospholipids Glycolipids: some are neutral some are charged present only on the non-cytosolic leaflet Lysosomal storage diseases - gangliosides

10. PE & PS PC & SM Cholesterol - about equal in quantity to phospholipid; stiffens membranes, reduces permeability, inhibits phase changes

11. PE & PS PC & SM

12. Lipid Rafts: Specialized membrane regions Rich in sphingolipids & cholesterol Better accommodate certain proteins Involved in membrane transport & signal transduction

13. 1. Membrane Organization and the Plasma Membrane 1b. Integral and peripheral proteins

14. 1 - Single pass a-helix 2 - Multi-pass a-helix 3 - Rolled-up b-sheet (b-barrel) 4 - a-helix in one layer 5 - lipid anchor 6 - oligosaccharide linker to phosphatidylinositol (non-cytosolic monolayer) 7, 8 - non-covalent interactions with integral membrane proteins (peripheral proteins)

15. Bacteriorhodopsin Photosynthetic reaction center (R. viridis)

16. INTEGRAL PROTEIN BEHAVIOR -Some exhibit lateral diffusion -Some are anchored in place -Orientation is maintained

17. Self-assembly into aggregates Tethered to extracellular molecules Tethered to intracellular molecules Bind to proteins on adjacent cell Mechanisms to Organize Proteins in Membranes

18. Cell junctions can also establish unique membrane domains

19. 1. Membrane Organization and the Plasma Membrane 1c. Glycocalyx

21. 1. Membrane Organization and the Plasma Membrane 1d. Cytoskeletal associations

22. Cytoskeletal associations….

24. 1. Membrane Organization and the Plasma Membrane 1e. Functions of the plasma membrane

25. FUNCTIONS OF THE PLASMA MEMBRANE 1. Protection and identification 2. Semi-permeable barrier

26. FUNCTIONS OF THE PLASMA MEMBRANE 1. Protection and identification 2. Semi-permeable barrier 3. Transport - Passive and facilitated diffusion, active transport 4. Endocytosis and exocytosis Endocytosis - transport via membrane flow

27. FUNCTIONS OF THE PLASMA MEMBRANE 1. Protection and identification 2. Semi-permeable barrier 3. Transport - Passive and facilitated diffusion, active transport 4. Endocytosis and exocytosis 5. Sensing environmental conditions - membrane receptors a. Ion channel-linked e.g., acetylcholine receptor at neuromuscular junction Can activate ion channels or other enzymes (e.g., epinephrine, serotonin, glucagon receptors) e.g., cytokine and growth factor receptors b. G protein-linkedc. Enzyme-linked

28. 2. Organelles 2a. Ribosomes and the Endoplasmic Reticulum

36. Membrane, lumenal and secreted proteins made by RER Cytoplasmic proteins are made by ‘free’ ribosomes

40. The oligosaccharide chains of N-linked glycoproteins are assembled on dolichol and transferred to proteins as they spool into the ER lumen

41. MOST of the proteins made by the RER are glycosylated (branched and N-linked). FEW cytoplasmic proteins are glycosylated (mostly simple and O-linked) There is a special class of extraordinarily heavily glycosylated proteins called PROTEOGLYCANS; these proteins are made in the ER but are glycosylated (via an O- linkage - linkage to serine or threonine) either in the Golgi apparatus or outside the cell. Proteoglycans are secreted by cells and make up part of the extracellular matrix.

42. CHAPERONES help nascent proteins fold correctly (present in both cytoplasm and ER). Misfolded proteins are ubiquinated and destroyed by PROTEASOMES. Proteasomes are located in the cytoplasm: misfolded ER proteins are transported into the cytoplasm by a membrane translocase complex for ubiquination and disposal. Proteasome Protein misfolding is believed to be the primary cause of Alzheimer's disease, Parkinson's disease, Huntington's disease, Creutzfeldt-Jakob disease, cystic fibrosis, Gaucher's disease and many other degenerative and neurodegenerative disorders

43. OTHER FUNCTIONS OF ENDOPLASMIC RETICULUM: -Lipid synthesis: delivery to Golgi, lysosomes, endosomes, plasma membrane is by membrane flow; delivery to mitochondria and peroxisomes is via exchange proteins -Calcium regulation: ER sequesters and releases Ca++ -Detoxification: Cytochrome p450 enzymes