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27 Cards in this Set

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Steps in protein synthesis?
Initiation, elongation, termination.
Protein synthesis: Initiation.
A ribosome attaches to the mRNA and stars to code the FMet codon (AUG, GUG or UUG).
Protein synthesis: Elongation.
tRNA brings the corresponding amino acid to each codon as the ribosome moves down the mRNA strand.
Protein synthesis: Termination.
Reading of the final mRNA codon which ends the synthesis of the peptide chain and releases it.
What are the protein post translational modifications?
Trimming, Covalent alterations, proteasomal degradation.
Posttranslational modification: Trimming.
Removal of N- or C- terminal pro-peptides from zymogens togenerate mature proteins.
Posttranslational modification: Covalent alterations.
Phosphorylation, Glycosylation, Hydroxylation.
Posttranslational modification: Proteosomal degradation.
Attachment of ubiquitin to defective proteins to tag them for break down.
Enzyme regulation methods?
Enzyme concentration alterations, covalent modification, proteolytic modification, allosteric regulation, pH, temperature and transcriptional regulation.
What are the cell cycle phases?
G1, S phase, G2, Mitosis.
What are the cells that remain in the G0 phase and regenerate from stem cells?
Neurons, skeletal and cardiac muscles, RBCs.
What are the cells that enter the G1 state from G0 when stimulated?
Stable cells: Hepatocytes, Lymphocytes.
What are the cells that never go to G0 and divide rapidly with a short G1?
Labile cells: Bone marrow, gut epithelium, skin, hair follicles.
Where in the cell are N-Linked oligosaccharides added to proteins?
RER.
What do Nissl-bodies synthesize?
Enzymes and peptide neurotransmitters.
Cells rich in RER?
Mucus secreting goblet cells of the small intestine and anti-body secreting plasma cells.
Cell site where steroid synthesis and detoxification of drugs and poisons take place?
SER.
Cells rich in SER?
Hepatocytes, steroid hormone producing cells of the adrenal cortex are rich in cells.
Failure of addition of mannose-6-phosphate to lysosome proteins, enzymes are secreted outside the cell instead of being targeted to the lysosome.
I-cell desease also refered to as mucolipidosis II (ML II).
Coarse facial features, clouded corneas, restricted joint movement, and high plasma levels of lysosomal enzymes. Often fatal in children.
I-cell disease.
Kartagener's syndrome.
Immotile cilia due to dynein arm defect. Results in male and female infertility, bronchiectasis and recurrent sinusitis.
Plasma membrane composition?
Asymmetric fluid bilayer. Cholesterol 50%, phospholipids 50%, sphingolipids, glycolipids and proteins.
Major component of RBC membranes, of myelin, bile and surfactant.
Phosphatidylcholine.
Where is the ATP site on a sodium pump?
Cytoplasm side.
How many K and how many Na does a sodium pump move for each ATP?
3 Na+ go out and 2 K+ come in.
How does Ouabain work?
Inhibits the sodium pump. Binds to K+ site.
What drugs inhibit the Na+ K+ ATPase causing an increase in cardiac contractility.
Cardiac glycosides.