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55 Cards in this Set

  • Front
  • Back
dissociation and sorting of ligands from receptors

What pathway?
early endosome
recycling of membrane proteins back to the membrane

What pathway?
early endosome
recycling CLATHRIN back to the plasma membrane to form coated pits.

What pathway?
early endosome
lysosomal enzymes destined for the lysosome have their SIGNAL PATCH tagged with ? in what organelle?
Mannose-6 Phosphate (M6P)

cis-GOLGI apparatus
Where are M6P receptors found?
Golgi
Lysosomes
Early and Late Endosomes
What causes the release of lysosomal enzymes from the M6P receptor?
ACIDITY of the late endosome
Where are EARLY ENDOSOMES found?


LATE ENDOSOMES?
near the membrane


near Golgi and Nucleus
Endosomal membranes contain ? that help acidify their interior.
H+ / ATP pump
What transports substances between Early and Late Endosomes?
multivesicular bodies
What are the FOUR possible fates of Receptor-Ligand Complexes sorted in the Early Endosome?
Receptor Recycled || Ligand Degraded

Receptor and Ligand RECYCLED

Receptor and Ligand DEGRADED

Transcytosis (both receptor and ligand transported through the cell)
What is an example of Transcytosis?
secretion of IgA

--both receptor and ligand transported through the cell
What are the 5 hydrolytic enzymes found in lysosomes?

PNGLP
Proteases

Nucleases

GLycosidases

Lipases

Phospholipases
Describe the 3 specialized features of the lysosomal membrane.
Glycosylated Proteins (prevents hydrolytic digestion)

Transport Proteins (move final product of digestion into cytoplasm)

Proton Pumps (acidify interior pH 4.7)
Why are leaked lysosomal enzymes practically inactive in the cytoplasm?
pH 7.2 --cytoplasm

pH 4.7 --lysosome
Drug use to treat malaria.

--raises the pH of the lysosome inactivating the enzymes
Chloroquine
True or False

LYSOSOME MEMBRANE PROTEINS can reach the lysosome via M6P pathway
FALSE

--Constitutive Secretory Pathway
or
--Golgi Derived Secretory Pathway
LYSOSOME MEMBRANE PROTEINS reach the lysosome by what 2 pathways?
Constitutive Secretory Pathway


Golgi Derived Secretory Pathway
Lysosome Membrane Protein Pathway

---exit the cell and make it back to the lysosome through the Endocytic Pathway
Constitutive Secretory Pathway
Lysosome Membrane Protein Pathway

---travel in CLATHRIN COATED VESICLES to Late Endosomal compartment where tSNARES and vSNARES assure their correct destination
Golgi Derived Secretory Pathway
What are the 3 Routes materials destined for degradation by the lysosome?
Phagosome (large extracellular particles)

Endosomes (small extracellular particles)

Autophagy (INTRAcellular particles large and small)
Cytoplasmic proteins and entire organelles are targets of degradation by the lysosome.
Autophagy
What are the 3 types of AUTOPHAGY?
Macroautophagy

Microautophagy

Chaperone-Mediated Autophagy
in MACROAUTOPHAGY a portion of cytoplasm or an organelle is surrounded by a membrane from the ? to form a ?
membrane from ER !!!!!!

autophagosome
in MICROAUTOPHAGY how are small cytoplasmic soluble proteins internalized in lysosomes?
Invagination
Whatspecial chaperone protein helps bind to SPECIFIC proteins to be degraded and transports them THROUGH the lysosomal membrane
hsc73
AZUROPHILIC granules of neutrophils are ?
lysosomes
? are lysosomes that contain products which cannot be broken down and often remain for teh life of the cell.
Residual Bodies
What is Tay-Sach's disease?
a lysosomal GALACTOSIDASE deficiency in neurons
? degrade INDIVIDUAL PROTEIN MOLECULES within the cell
proteosomes
? degrades BULK MATERIAL within the cell
lysosomes
Damaged proteins (denatures or oxidizies proteins) are tagged with ?
pollyubiquitin
3 proteins that covalently attach ubiquitin to damaged proteins?
E1 E2 E3 Ligases
After transcription occur-- what type of genetic code has been created? (be specific)
pre-mRNA
describe the pre-mRNA to mRNA process
splice introns

join exons

addition of 3' polyA tail

addition of 5' methyl guanosine cap
groupos of ribosomes that are translating the same strand of mRNA and can make many copies of the same protein
POLYSOMES (polyribosomes)
Antibiotics target differences in prokaryotic and eukaryotic ?
ribosomes
a series of interconnected membrane-limited flattened sacs in the rER are called ?
cisternae
True or False

rER may be continuous with the nuclear envelope.
True
What type of staining is associated with mRNA ?
basophilic
? is the portion of the cytoplasm that is basophilic OR in secretory cells the ? is the rER
Ergastoplasm
rER is well developed in ? cells
secretory cells
describe the ER signal sequence in the translated amino acid chain
series of HYDROPHOBIC amino acids at the beginning
the ER SIGNAL SEQUENCE becomes attached to a ? that binds a DOCKING PROTEIN on the cytoplasmic surface of the ER membrane
Signal Recognition Particle (SRP)
the DOCKING PROTEIN helps align the ribosome with a ? which is an IMP of the rER
Translocation
? is when the protein gets inserted into and passes through the membrane into the cisterna as it is translated
cotranslational insertion
A protein that has its signal sequence cleaved in the rER lumen will be found where in the cell?
the protein will be SECRETED out of the cell
membrane proteins will pass back and forth through the ER membrane as new ? are translated --which stops the threading process and permanently anchors the protein in the membrane.
Hydrophobic Signal Domain
What type of protein modification occurs in the cisterna of the rER? (4)
Glycosylation

Disulfide and Internal hydrogen bond forming

Folding

Partial Subunit Assembly
vesicles covered with ? mediate bi-directional transport of proteins between rER and Golgi
coatemer (COP)
RETROGRADE transport (Golgi >> ER) of vesicles are coated in ?
COP-I
ANTEGRADE transport (rER >> Golgi) of vesicles coated in ?
COP-II
Free ribosomes synthesize cytoplasmic proteins which do not have a ?
signal sequence
where are MITOCHONDRIAL ENZYMES synthesized?
in the cytoplasm by Free Ribosomes
? is a barrel-shaped protein complex composed of 7 PROTEINS including ? and ?
PROTESOME

-proteases
-ATPase
? in neurons are due to the basophilic staining of rER ribosomes + free ribosomes (due to ? on the mRNA associated with these ribosomes)
Nissl Bodies


due to phosphate groups