Cell Structure and Function Flashcards

1
Q

Name the four major categories of membrane phospholipids.

A

Amino (phosphatidyl-ethanolamine, phosphatidyl serine (-))

Choline (phosphatidyl-choline, sphingo-myelin) Phosphoglycerides (Aminos + Phos-choline) Sphingolipid (Sphingo-myelin)

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2
Q

Name three effects of cholesterol in the phospholipid membrane.

A

stiffens membrane
reduces permeability
inhibits phase changes

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3
Q

Which phospholipid eventually flipped and face cytosolic surface as membrane moves from ER to Golgi to membrane?

A

Amino Phospholipids

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4
Q

What is a signal for cell death with repect to phospholipids?

A

The flipping of the negative phosphatidyl-serine to non-cytosolic side. Scramblase flips sporatically so charge is evened out.

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5
Q

Glycolipids face the [ ] side of the cell and prevent [ ] from interacting with the small intestine.

A

Non-cytosolic side; digestive enzyme.

They also form thicker patches (lipid rafts) in the small intestine for protection.

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6
Q

Inositol phospholipids have multiple locations to be phosphorylated and are crucial to cell function (T/F)

A

T

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7
Q

Name some functions of phosphatidylinositol:

A

Serving as a binding site for cytosolic membrane-associated proteins and enzymes
Anchoring proteins to the plasma membrane
Cell signaling, including protein kinase C and Ca++ second messenger regulation
Identifying specific organelle membranes and regulating organelle function
Controlling vesicular trafficking
Modulating ion channel activity
Regulating secretion
Chemotaxis and immune cell function
Neuronal growth and synaptic signaling

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8
Q
Which of these movements for phospholipids is rare?
Flexing
Rotation, 
Flipping 
Lateral Movement
A

Flipping (if not accompanied by flipase/scramblase)

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9
Q

Choline phospholipids eventually end up on which side?

A

Non-cytosolic leaflet

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10
Q

Flipases do not show specificity for which PPlipid is flips while scramblases show specificity (T/F)

A

F, the opposite is true: Flipases = selective, Scramblases = no specificity

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11
Q

How can membrane proteins organize themselves?

A

Attach to extra or intracellular matrix, bind to another cell, or aggregate.

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12
Q

What is the name of the long protein where mutation sites lead to muscular dystrophy?

A

Dystrophin

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13
Q

Name one similarity and one difference of Hereditary spherocytosis when comparing to muscular dystrophy.

A

Similar in that it involves mutations for proteins involved in mechanical support of plasma membrane, but it’s different in that it affects RBC, not muscle cells.

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14
Q

Membrane protein orientation is determined by:

A

The number and orientation of the stop/start sequence(s).

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15
Q

N-linked glycosylated proteins are attached to [ ] and it is located on the [ ] side.

A

Asparagine; non-cytosolic side.

Because the glycosyl transferase enzymes that do this are located in the ER lumen, the sugar groups of these glycoproteins are always located on the non-cytosolic side of membranes.

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16
Q

O-linked glycosylated proteins are attached to [ ] and the sugar is added in the [ ].

A

Serine and Threonine; Golgi

17
Q

How do misfolded proteins get degraded?

A

They leave the ER, are ubiquitanated, and fed through proteasomes that are only located in the cytosol.

18
Q

What are the three major destinations that the golgi transports vesicles?

A
  • Lysosomes
  • Secretory vesicles
  • Plasma membrane
19
Q

What is the connection between the golgi and N-linked glycoproteins?

A

The Golgi modifies those glycoproteins when they arrive from the ER.

20
Q

What are the three pathways through which vesicle leave from the Golgi?

A
  1. ) Constituted: Default, all cells do this to recycle PM.
  2. ) Regulated: Secretes in specific manner
  3. ) Formation of Lysosomes
21
Q

Name the three pathways that lead to a lysosome.

A

Autophagy (a survival cell mechanism), phagocytosis, and fusion with endosome to eventually form a lysosome.

22
Q

Caveolin inserts into the cytosolic leaflet, causes it to curve, and forms a vesicle. (T/F)

A

T

23
Q

These are the two types of coat proteins. (Can you name their functions?)

A

Clathrin - distal transport (PM, Lysosome, endosomes)

Coatamer (cop) proteins - proximal transport between ER and golgi

24
Q

Cargo proteins and clathrin have no link. (T/F)

A

F, adapter proteins do this.

25
Q

How do GDP and GTP affect COP-I and COP-II?

A

GTP turns on G proteins, GDP turns G protein off when they are binding the COP proteins. GEFs turn on, GAFs turn off, small G proteins.

26
Q

What are the three sets of proteins that aid in accurate delivery and fusion of vesicles?

A

Rab, Rab effectors, and SNAREs. All of these are aided by inositol phospholipids.