Introduction and protein sorting

Transcription

1 Introduction and protein sorting

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3 Membrane proteins Major components of cells Nucleic acids Carbohydrates Proteins Lipids (50% of mass of plasma membranes, 30% of mitochondrial membranes, 80% of myelin sheeth), species dependent

4 Composition and properties of membranes Lipids: phospholipids, glycolipids, and cholesterol Cholesterol: animal, rigidity, fluidity It is not present in bacteria or plant cells

5 Composition and properties of plasma membranes Phospholipids are asymmetrically distributed between the two halves of the membrane bilayer The outer leaflet: choline, sphingomyelin The inner leaflet: ethanolamine, serine, inositol (minor) inositol has a role in cell signaling. serine stimulates apoptosis when extracellular.

6 Lipid rafts Clusters of cholesterol and sphingolipids (longer and straighter). Sphingolipids provide an ordered lipid environment. Rafts are enriched in glycosylphosphatidylinositol (GPI)- anchored proteins, as well as proteins involved in signal transduction and intracellular trafficking (endo- & exocytosis).

7 Lipid rafts and diseases HIV virus Budding may occur from lipid rafts Influenza virus Raft-associated glycoproteins in envelope Prion disorder Normal prion protein (PrPc) is converted to abnormal proteins (PrPsc) in lipid rafts (aggregation).

8 Membrane proteins Peripheral: indirect, mainly ionic, ph or salt. Integral: transmembrane α-helix: a.a non-polar β-sheet: barrel Detergents

9 Lipid-anchored membrane proteins Myristoylation: N-terminus glycine Palmitoylation: sulfur of internal cysteine Prenylation: linking of "isoprene"-based groups Farnesylation: RAS (oncoprotein), 95% of pancreatic cancers sulfur of C-terminus cysteine Glycolipid (glycosyl phosphatidylinositol) anchors GPIs The carbohydrate bridges the protein with the fatty acid chains of the phospholipid (usually ethanolamine)

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11 Protein mobility Proteins (as lipids) are able to diffuse laterally Mobility restrictors: Cytoskeleton association Specific membrane domains such as tight junctions Lipid composition (e.g. lipid rafts)

12 Glycocalyx A carbohydrate coat Formed by oligosaccharides of glycolipids and transmembrane glycoproteins Functions: Cell-cell interactions (e.g, leukocytes and selectins) Protection from ionic and mechanical stress Formation of a barrier for microorganisms

13 Endoplasmic reticulum (ER) It is a network of membrane-enclosed tubules and sacs (cisternae) that extends from the nuclear membrane throughout the cytoplasm It is the largest organelle of most eukaryotic cells Rough ER: covered by ribosomes Smooth ER: lipid metabolism, Ca ++ stores Transitional ER: exit of vesicles to Golgi apparatus Microsomes

14 Protein sorting Free ribosomes: cytosolic, nuclear, peroxisomal, and mitochondrial proteins Membrane-bound ribosomes: others (most proteins) are transferred into the ER while they are being translated (cotranslational translocation) Stay there or sorted: golgi, peroxisomal membrane, vesicles, plasma membrane, or secreted extracellularly

15 Ribosomal and protein targeting All protein synthesis initiates on ribosomes that are free in the cytosol. Ribosomes are targeted for binding to the ER membrane by the amino acid sequence of the polypeptide at the amino terminus called a signal sequence (hydrophobic, 20, basic). It is then cleaved from the polypeptide chain during its transfer into the ER lumen, preproteins!.

16 Mechanism of translocation (co-traslational translocation) Step 1: recognition by the signal recognition particle (SRP), blockage Step 2: binding; SRP escorts the complex to the ER membrane (SRP receptor) Step 3: release; SRP is released, the ribosome binds to a translocon, and the signal sequence is inserted into a membrane channel Step 4: Translation resumes, and the growing polypeptide chain is translocated across the membrane Step 5: Cleavage of the signal sequence by signal peptidase releases the polypeptide into the lumen of the ER

17 Mechanism of translocation Translocon

18 Posttranslational translocation Free ribosomes, remain unfolded (chaperones) Signal sequences recognized by a protein complex associated with the translocon The protein complex is also associated with a chaperone protein (BInding Protein - BiP), which drives protein translocation into the ER Translocon

19 Pathways of protein sorting Lumen of ER or Golgi is similar to outside ER lumen: Secretory, ER, Golgi apparatus, and lysosomal proteins ER membrane: Membranous proteins Considerations Single vs. multiple membrane spanning region Orientation of N- and C-termini

20 Insertion of a membrane protein A cleavable amino-terminal signal sequence that initiates translocation across the membrane, and A transmembrane stop-transfer sequence that anchors the protein in the membrane Cleave signal sequence Stop transfer Close channel Move laterally Signal peptidase Close channel

21 Insertion of a multi-domain membrane protein Close channel Re-open channel

22 Once inside Assembly of multisubunit proteins Protein folding, assisted by the molecular chaperone, that keep protein unfolded until properly folded (e.g. BiP) Disulfide bond formation by providing an oxidizing environment (the cytosol has a reducing environment) assisted by protein disulfide isomerase (PDI)

23 Also, once inside N-acetyl glucosamine is the first sugar Addition of glycolipid anchors to some plasma membrane proteins. Carboxy-terminal Functions of glycosylation: 1.Prevents protein aggregation in the ER 2.Helps in further protein sorting Specific glycosylation sequence Asn-X- Ser/Thr

24 Fate of a glycoprotein ER-associated degradation (ERAD) Calreticulin, a chaperone, releases it when glucose is removed A folding sensor binds to the protein If correctly folded, the protein moves to transitional ER If misfolded, glucose is added and calreticulin refolds the proteins. If severely folded, the protein is degraded.

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26 Unfolded protein response (UPR) BiP initiates the process Outcome: 1. General protein synthesis inhibition 2. Expression of chaperones 3. Activity of proteasomes Activate UPR target genes such as chaperones

27 Protein sorting and retention Many proteins with KDEL sequence (Lys-Asp-Glu-Leu) at C-terminus are retained in the ER lumen If sequence is deleted, the protein is transported to the Golgi and secreted from the cell Addition of the sequence causes a protein to be retained in the ER The retention of some transmembrane proteins in the ER is dictated by short C- terminal KKXX sequences. Proteins bearing the KDEL and KKXX sequences appear to be recycled back to the ER

28 Protein sorting and retention Membrane proteins contain di-acidic or di-met signal sequences. They can also function as carriers of GPI-anchored and lumenal proteins.

29 Synthesis of phospholipids in ER Enzymes (acyl transferase) are associated with the outer leaflet of the membrane

30 Translocation of phospholipids across the ER membrane Flippases

31 Synthesis of ceramide

32 Synthesis of other lipids Steroid hormones are synthesized from cholesterol in ER Large amounts of smooth ER are found in steroid-producing cells, such as those in the testis and ovary Smooth ER is abundant in the liver, where it contains enzymes that metabolize various lipid-soluble compounds. The detoxifying enzymes inactivate a number of potentially harmful drugs (e.g., phenobarbital) by converting them to watersoluble compounds that can be eliminated from the body in the urine

33 ER-Golgi intermediate compartment (ERGIC)

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36 Golgi apparatus and vesicular transport Functions of Golgi Further protein processing and modification (e.g. glycosylation) Protein sorting Synthesis of glycolipids and sphingomyelin

37 Structure of the Golgi 1. Cis Golgi network protein entrance 2. Golgi stacks: medial & trans most of the metabolic activities 3. Trans Golgi network sorting and distribution center Protein modification takes place at all levels, endosomes

38 Processing of oligosaccharides in Golgi N-linked glycoproteins Lysosomal vs. Membrane

39 Processing of oligosaccharides in Golgi O-linked glycoproteins Proteins can also be modified by the addition of carbohydrates to the side chains of acceptor serine and threonine residues. The serine or threonine is usually linked directly to N-acetylgalactosamine, to which other sugars can then be added.

40 Lipid and Polysaccharide Metabolism in the Golgi Transfer of phosphorylcholine group is from phosphatidylcholine to ceramide. Sphingomyelin is synthesized on the lumenal surface. Addition of sugar residues. Glucose is added to ceramide on the cytosolic side and glucosylceramide then apparently flips and additional carbohydrates are added on the lumenal side of the membrane Ceramide is synthesized in the ER

41 Protein Sorting and Export In contrast to the ER, all of the proteins retained within the Golgi complex are associated with the Golgi membrane rather than being soluble proteins within the lumen Protein packaging mediated by cargo receptor processing in Immature secretory vesicles Regulated secretion after signaling from specialized vesicles Continuous, unregulated secretion

42 Transport to the plasma membrane of polarized cells This is accomplished by the selective packaging of proteins into transport vesicles from the trans Golgi or recycling endosomes Targeting is determined by special sequences (basolateral) or sugar modification (apical)

43 Processing of lumenal lysosomal proteins Addition of N- acetylglucosamine phosphates Removal of N- acetylglucosamine The enzyme recognizes a signal patch (a three-dimensional structural determinant) not a sequence

44 Transport of lysosomal proteins Lumenal: marked by mannose-6-phosphates bind to a mannose-6-phospahte receptor. Complexes are packaged into transport vesicles destined for late endosome, which mature into lysosomes. lysosomal membrane proteins are targeted by sequences in their cytoplasmic tails, rather than by mannose-6-phosphates.

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47 Formation & fusion of a transport vesicle Vesicular transport Coat disassembly Vesicular docking & fusion

48 Coat proteins

49 Formation of clathrin-coated vesicles

50 Role of ARF1 (G-protein) (ADP-ribosylation factor) 1. Activation of Arf1 by GEF 2. Recruitment of AP1 (not shown) and clathrin 3. Formation of Arf1-clathrin-receptor-cargo complex 4. Formation of vesicle 5. Budding and transport of vesicle 6. Inactivation of Arf1 and disassembly of coat 7. Vesicle fusion

51 Players of vesicle fusion SNARE & Rab Rab: G-protein Function in several steps of vesicle trafficking SNARE: formation v-snares-t-snares complexes Soluble NSF(N-ethylmaleimide-sensitive factor) Attachment Protein) REceptor Effector proteins allow for specific interaction

52 The mechanism of fusion Interaction of effector proteins Closer vesicle-target Fusion Tethering, hydrolysis of GTP, SNARE interactions Disassembly of SNARE complex

53 RECAP 1. Interaction between different effector proteins 2. Tethering of the SNAREs 3. Hydrolysis of the GTP to GDP 4. The snares interact with each other 5. The vesicle membrane gets closer to the plasma membrane and then it dissolves by fusing into it 6. The SNARE complex is disassembled 7. The vesicle becomes part of the membrane

54 Exocytosis Exocyst: A complex of 8 different proteins

55 Griscelli syndrome (GS) A rare genetic condition Many Types: GS1, GS2, GS3 Mutations in MYO5A, RAB27A and MLPH genes that encode the MyoVA- Rab27a-Mlph protein complex that function in melanosome transport & fusion

56 Griscelli syndrome (GS) Pigmentary dilution of the skin, silver-grey hair, melanin clumps within hair shafts Mature melanosomes accumulate in the centre of melanocytes