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Protein degradation rate varies 100x

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Presentation on theme: "Protein degradation rate varies 100x"— Presentation transcript:

1 Protein degradation rate varies 100x
Most have motifs marking them for polyubiquitination: taken to proteosome & destroyed Other signals for selective degradation include PEST & KFERQ PEST : found in many rapidly degraded proteins Deletion increases t1/2 10x, adding PEST drops t1/2 10x Sometimes targets poly-Ub Recent yeast study doesn’t support general role KFERQ: cytosolic proteins with KFERQ are selectively taken up by lysosomes in chaperone-mediated autophagy under conditions of nutritional or oxidative stress.

2 Protein degradation in bacteria
Also highly regulated, involves chaperone-like proteins Lon (also in mito)

3 Protein degradation in bacteria
Also highly regulated, involves chaperone like proteins Lon Clp (also in chloroplasts)

4 Protein degradation in bacteria
Also highly regulated, involves chaperone like proteins Lon Clp FtsH in IM (also in cp and mito)

5 PROTEIN TARGETING All proteins are made with an “address” which determines their final cellular location Addresses are motifs within proteins

6 PROTEIN TARGETING All proteins are made with “addresses” which determine their location Addresses are motifs within proteins Remain in cytoplasm unless contain information sending it elsewhere

7 PROTEIN TARGETING Targeting sequences are both necessary & sufficient to send reporter proteins to new compartments.

8 PROTEIN TARGETING 2 Pathways in E.coli Tat: for periplasmic redox proteins & thylakoid lumen!

9 2 Pathways in E.coli Tat: for periplasmic redox proteins & thylakoid lumen! Preprotein has signal seq S/TRRXFLK

10 2 Pathways in E.coli Tat: for periplasmic redox proteins & thylakoid lumen! Preprotein has signal seq S/TRRXFLK Make preprotein, folds & binds cofactor in cytosol

11 2 Pathways in E.coli Tat: for periplasmic redox proteins & thylakoid lumen! Preprotein has signal seq S/TRRXFLK Make preprotein, folds & binds cofactor in cytosol Binds Tat in IM & is sent to periplasm

12 2 Pathways in E.coli Tat: for periplasmic redox proteins & thylakoid lumen! Preprotein has signal seq S/TRRXFLK Make preprotein, folds & binds cofactor in cytosol Binds Tat in IM & is sent to periplasm Signal seq is removed in periplasm

13 2 Pathways in E.coli http://www.membranetransport.org/
Tat: for periplasmic redox proteins & thylakoid lumen! Sec pathway SecB binds preprotein as it emerges from rib

14 Sec pathway SecB binds preprotein as it emerges from rib & prevents folding

15 Sec pathway SecB binds preprotein as it emerges from rib & prevents folding Guides it to SecA, which drives it through SecYEG into periplasm using ATP

16 Sec pathway SecB binds preprotein as it emerges from rib & prevents folding Guides it to SecA, which drives it through SecYEG into periplasm using ATP In periplasm signal peptide is removed and protein folds

17 Sec pathway part deux SRP binds preprotein as it emerges from rib & stops translation Guides rib to FtsY FtsY & SecA guide it to SecYEG , where it resumes translation & inserts protein into membrane as it is made

18 Periplasmic proteins with the correct signals (exposed after cleaving signal peptide) are exported by XcpQ system

19 PROTEIN TARGETING Protein synthesis always begins on free ribosomes in cytoplasm

20 2 Protein Targeting pathways
Protein synthesis always begins on free ribosomes in cytoplasm 1) proteins of plastids, mitochondria, peroxisomes and nuclei are imported post-translationally

21 2 Protein Targeting pathways
Protein synthesis always begins on free ribosomes In cytoplasm 1) proteins of plastids, mitochondria, peroxisomes and nuclei are imported post-translationally made in cytoplasm, then imported when complete

22 2 Protein Targeting pathways
Protein synthesis always begins on free ribosomes In cytoplasm 1) Post -translational: proteins of plastids, mitochondria, peroxisomes and nuclei 2) Endomembrane system proteins are imported co-translationally

23 2 Protein Targeting pathways
1) Post -translational 2) Co-translational: Endomembrane system proteins are imported co-translationally inserted in RER as they are made

24 2 pathways for Protein Targeting
1) Post -translational 2) Co-translational: Endomembrane system proteins are imported co-translationally inserted in RER as they are made transported to final destination in vesicles

25 SIGNAL HYPOTHESIS Protein synthesis always begins on free ribosomes in cytoplasm in vivo always see mix of free and attached ribosomes

26 Protein synthesis begins on free ribosomes in cytoplasm
SIGNAL HYPOTHESIS Protein synthesis begins on free ribosomes in cytoplasm endomembrane proteins have "signal sequence"that directs them to RER Signal sequence

27 SIGNAL HYPOTHESIS Protein synthesis begins on free ribosomes in cytoplasm endomembrane proteins have "signal sequence"that directs them to RER “attached” ribosomes are tethered to RER by the signal sequence

28 SIGNAL HYPOTHESIS Protein synthesis begins on free ribosomes in cytoplasm Endomembrane proteins have "signal sequence"that directs them to RER SRP (Signal Recognition Peptide) binds signal sequence when it pops out of ribosome & swaps GDP for GTP

29 SIGNAL HYPOTHESIS SRP (Signal Recognition Peptide) binds signal sequence when it pops out of ribosome & swaps GDP for GTP 1 RNA & 7 proteins

30 SIGNAL HYPOTHESIS SRP binds signal sequence when it pops out of ribosome SRP stops protein synthesis until it binds “docking protein”(SRP receptor) in RER

31 SIGNAL HYPOTHESIS SRP stops protein synthesis until it binds “docking protein”(SRP receptor) in RER Ribosome binds Translocon & secretes protein through it as it is made

32 SIGNAL HYPOTHESIS SRP stops protein synthesis until it binds “docking protein”(SRP receptor) in RER Ribosome binds Translocon & secretes protein through it as it is made BiP (a chaperone) helps the protein fold in the lumen

33 SIGNAL HYPOTHESIS Ribosome binds Translocon & secretes protein through it as it is made secretion must be cotranslational


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