5.ER - cell biology
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Transcript of 5.ER - cell biology
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Cell BiologyCell Biology
S. Rahgozar,PhD
University of IsfahanFaculty of Science
4. Protein sorting and transport
4.1. The Endoplasmic Reticulum
1392-93
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The Endoplasmic Reticulum
The largest organelle in mosteukaryotic cells
ER membrane is 50% of cellmembrane
Space enclosed by ER is 10% of thetotal cell volume
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ER domains:
Rough ER (+ ribosomes)
Smooth ER where lipid metabolismhappens
Transitional ER where vesicles exitto the Golgi apparatus
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Isolation of rough ER
Rough ERFolding
ProcessingGolgi
apparatus Sorting
Processing
Transport
Secretoryvesicles
Inside
Outside
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Overview of protein sorting
Golgi apparatus
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The secretory pathway
Pancreatic cell
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Incorporation of secretory proteins into cytoplasm/microsomes
The signal sequence of growth hormone
20 hydrophobic amino acid proceeded by a basic aa (ie; Arg)
N
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Cotranslational targeting of secretory proteins to the ER
SRP: signal recognitionparticle
Translocon:membrance channel
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Structure of the SRP
Blue: SRP proteins
Orange: SRP RNA including2 flexible hinge regions
Green: Signal sequence
The signal sequence on the nascent protein binds to apocket in the SRP proteins
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Translocons are
Complexes of 3 membrane proteins called the Sec61 proteins
Conserved among prokaryotic and eukaryotic cells
Signal sequence Short hydrophobic side chains in translocon neck
Opening of the translocon channel
Transfer of the growing polypeptide chain through the translocon
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Translocation of proteins into the ER after their translation
HSP 70
BIP acts as a ratchet todrive theposttranslationaltranslocation of proteinsinto the ER.
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Insertion of proteins into the ER membrane
Integral membrane proteins span the membrane via α-helical regions of 20 to25 hydrophobic amino acids, which can be inserted in a variety of orientations.
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Transport of integralmembranes
Proteins destined for the innernuclear membrane do not transferby vesicles, but move laterally inthe plane of the membrane.
Transportvesicle
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Insertion of integral proteins
o Insertion of a membrane protein with a cleavable signal sequenceand a single stop-transfer sequence
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o Insertion of a membrane protein with no cleavable signal sequence
?
Orientation of theprotein depends onthe orientation of thesignal sequence
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o Insertion of a protein that spans the membrane multiple times
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Transport of integralmembranes
Proteins destined for the innernuclear membrane do not transferby vesicles, but move laterally inthe plane of the membrane.
Transportvesicle
Specific tansmembrane sequences located
in the inner nuclear membrane proteins
may alter their interaction with the
translocon and signal their transport to the
inner nuclear membrane where they are
retained by interactions with nuclear
components such as lamins or chromatin
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Types of post translational modification of proteins in the ER
o Protein folding in the ER
o Formation of disulfide bonds (S-S)
Formation of S-S bonds is facilitated by PDI , the enzyme which is located inthe ER lumen.
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o Glycosylation
14 sugar residues
3
Asn-X-Ser/ThrOligosaccharyltransferase
Glycoslation
Helps to prevent protein aggregation
Provides signals for subsequent sorting in the secretory pathway
9
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o Addition of glycoprotein phosphatidyl inositol (GPI) anchor
Yellow: inositol
Red: mannose
Blue: Glucosamine
Purple: N-acetylgalactosamine