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33 Cards in this Set

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phagocytosis
cell eating
Phagocytosis occurs mainly in which types of cells?
mainly in specialized cells like neutrophils and macrophages
Pinocytosis. in which cells types? ingests what?
cell drinking=ingestion of solutes such as protein hormones, macromolecule complexes in liquid medium

is prevanlent in all cell types
Receptor Mediated Endocytosis (RME) is the ____dependent _____of what?
clathrin dependent ingestion fo receptor bound material in clathrin-coated pits
Caveolae is __________ formed by _______ in______
the ingestion of small vesicles formed by aggregation of Caeolin in lipid rafts
Macropinocytosis
uptake of liquid in large vesicles formed by extensions of the plasma
name the 3 types of pintocytosis
RME, Caeolae, Macropinocytosis
Steps of RME
1) Ligands internalized specifically
2) sorted into clathrin coated pits in membrane
3) budding of pits from Plasma membrance to make clathrin vesicles (requires GTPase=Dynamin to pinch off)
Structure of Clathrin.
chain-link fence/cage/lattice when aggregates.
Function of Clathrin
1) distorts plasma membrane by building to produce vesicle
2)capture membrane receptors/bound molecules
In Endocytosis, binding of _____and _____creates _______change in opposite part of protein to allow what?
receptor and ligand creates conformational change in the opposite part of the protein to allow Adaptor Proetin 2 to bind to the specific AA sequence in the cytoplasmic tail domain of the receptor/clathrin coat
The ligand, receptor, (with trans membrane protein) and Adaptor protein connect to the_____ and get...?
clathrin cage on the outside of the cell and get sucked into like a black hole
First step of RME Trafficking: At the Early Endosome...
clathrin coat dissociates/vesicles fuse with Early Endosome
Second step of RME Trafficking: early endosome membrane contains _____ that lowers ____ and causes...?
H+pump that lowers pH of the lumen to 6.0, causing dissocation of the ligand from the receptor and triggers recycling of receptors back to plasma membrane
Sorting in the Early Endosomes creates 2 types of vesicles that bud from the early endosome. What are they?
1) transport (recycling) vesicles that carry receptors and membrance back to the plasma membrance

2)endocytic vesicles that carry ligand further on to the late endosome
Late Endosomes have pH of ___, fuse with ___ carrying_____ from trans Golgi tagged with ________
5.5 and fuse with transport vesicles carrying the lysosomal hydrolases from trans Golgi tagged withe Mannose 6Phosphate
Late Endosomes mature into Lysosomes by...?
1) sorting hydrolytic enzymes with ligand

2) recycling of endosome membrane proteins back to trans Golgi

3) lower pH to 5.0 for enzyme activation
Vesicles are transported along microtubules via...?

which protein goes + and which protein goes - ?
Dynein motor proteins (towards minus ends of MY) or Kinesins (toward the plus ends of MT)
Name some examples of Ligands. 9 categories
1) Hormones: insulin, glucagon, LH, Growth, Prolactin, TSH, TH
2) Growth Factors: Epidermal Growth Factor/Nerve Growth Factor
3) Lipoproteins, LDL, VLDL, HDL
4) Antibodies, IgE, IgG via Fc receptors
5) Vitamins: A,D, B12
6) Iron Binding Proteins: Transferrin
7)Toxins: Diptheria, Cholera
8) Viruses: adenovirus, rous sarcoma
In some cases, some growth factor receptors, want to downregulate endocytosis. What does this and how? what is this called?
MultiVesicular Bodies (MVB)
sort and degrade integral membrane proteins and help hormone desensitization by removing the receptors from the surface of the cell


Ex.) EGF-tagged for degradation by Ubiquitin
Describe function of Ubiquitin. What happens then?
Ubiquitin tags receptors to be sorted into small vesicles.

These vesicles bud from the late endosomes, accumulate in MVB, fuse with the lysosome, and are then degraded. Then hormone has less receptors to bind to on cell surface =desensitized
Caveolae are a mechanism of what?

Where are they abundant?
Mechanism of pinocytosis. ARE NOT RECEPTOR MEDIATED!

Abundant in vascular endothlial cells. Smooth muscles cells, fibroblasts and adipocytes.
Caveolins are what? Where are they located and what do they help make up?
Integral membrane proteins anchored into the plasma membrane in rigid lipid rafts, that help to make up caveolae.
Function of Caveolae:
1Endocytosis: byd as vesicles from plasma membrane/fuse with “caveosomes/early endosomes.

2) Transcytosis: bud as vesicles from cell surface, traverse the cell and fuse with plasma membrane at another location on cell surface
Lysosomes. Describe size, electron density, internal components?
variable in terms of size. Electron dense but not uniform. Lumen has many different types of Lysomal enzymes/acidic hydrolases.
Lysosomes have a ____ which is used for activating....?
proton pump (via ATP) lower pH to 5 for enzyme activation=fully active.
Glycosylation of membrane proteins in lysosomes serve as _______ to protect membrane against....?
glycoprotein lining to protect against it's own enzymes along the inner/luminal membrane
Lysosomes have membrane transporters for...?
release of digestion products (AA, sugars, lipids). You have to poop it out!
Formation of Lysosomes: Tag for lysosomal enzymes? binding through ____. Fuses with ______. Low ____ dissociates _____. What is recycled to trans golgi? How do lysosomes become mature? pH?
Draw it out!
1)Lysosomal enzyme tagged with Mannose 6-P in cis golgi
2)sort through golgi-trans golgi
3) M6Ps are not transmembrane, so have receptors that bind thru membrane to adaptor protein, then clathrin binds
4) clathrin coat sheds and then vesicle Fuses with late endosomes
5) Low pH (5.5) of Late Endosome dissociate M6P recepetors from enzymes
6)M6P receptors recycles back to trans golgi via transport vesicles
7)Late Endosomes mature into Lysosomes by sorting hydrolytic enzymes/lowering pH to 5.0 for enzyme activation
Lysomal Storage Diseases

If problem with lysomal enzymes-going to have problem...
digesting material that cells take up=diseases, especially in Tay Sachs
Tay Sachs=
a-Hexosamindidase A =accumulation of GM2 Gangliosides in brain-causes increase in Glial cells and abnormal growth of dendritic processes of neurons.

Mutation can’t break down gangliosides properly = accumulates+disrupts neural system
Gaucher’s Disease=
b-glucocerebrosidase accumulates in macrophages =heptamegaly/enlarged spleen
I-Cell Disease=
processing of mannose 6-p tag is defective. Cant sort lysosomal enzymes. Non specific. Lysosomes can’t degrade anything!