Term 1- Lec 5- Cell Membranes Flashcards

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1
Q

Components of Glycerophospholipids

A

2 FAs—Glycerol—Phosphate—X ; X can be choline, serine, etc. (Phosphatidylcholine, Phosphatidylserine)

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2
Q

Components of Sphingolipids

A

1 FA—Sphingosine (contains one long chain)—Phosphate—X. Ex: Sphingomyelin, Glycosphingolipids.

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3
Q

What is the most abundant lipid in membranes?

A

Glycerophospholipids (The typical phospholid shown in diagrams)

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4
Q

What is characteristic of glycophospholipids and why is it crucial to membrane properties/structure?

A

ONE of the FA tails has one or more CIS- bonds that cause a kink in the structure. This allows them to remain fluid for a wider range of temperatures.

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5
Q

What is the backbone of a glycophospholipid?

A

Glycerol

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6
Q

What is the backbone of a sphingolipid?

A

Sphingosine

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7
Q

Ceramide is made up of what two structures?

A

Sphingosine and a FA chain

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8
Q

Adding a sugar to ceramide creates what? What are these precursor to?

A

Glycolipids. They are found most commonly in NERVE TISSUES. They are precursors for Cerebrosides and Gangliosides.

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9
Q

What lipids are important in nerve tissues and prevalent in brain cell membranes?

A

Cerebrosides

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10
Q

What are the most complex sphingolipids; found primarily in a certain type of cells in the CNS? What type of cell are they primarily in?

A

Gangliosides. They are found in Ganglion Cells.

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11
Q

What are the components of Cholesterol?

A

1 FA—steroid ring structure—small polar head.

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12
Q

What effet does cholesterol have on membrane fluidity?

A

At High T, it prevents the membrane from becoming too fluid. At Low T, it lowers the point at which membranes become gel-like.

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13
Q

What membrane components are most common in the outer leaflet of the cell membrane?

A

Sphingomyelin, Glycolipid, Phosphatidylcholine, and Cholesterol

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14
Q

What membrane components are most common in the inner leaflet of the cell membrane?

A

Phosphatidylserine, Phosphatidylinositol, and Phosphatidylethanolamine

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15
Q

What are the components of Sphingomyelin?

A

(1 FA—Sphingosine)=Ceramide—Phosphate—Choline

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16
Q

What are the common components of a Lipid Raft?

A

Sphingomyelin, Glycolipids, Cholesterol, and GPI-anchored proteins

17
Q

What processes are lipid rafts necessart for?

A

Endocytosis and Receptor-Mediated Signaling

18
Q

5 types of movement exhibited by glycerolphospholipids and sphingolipids?

A

Lateral Diffusion, Rotation, Swing (tails swinging), Flexion (compression of tails), Transverse (flip-flop)

19
Q

What determines much of the functions of a membrane?

A

Protein portions. i.e. Myelin membrane is ~25% protein and Inner Mitochondrial membrane is ~75%

20
Q

What membrane component anchors most proteins to the outer leaflet?

A

GPI—Glycophosphatidylinositol.

21
Q

What is good about proteins being connect to GPI on the outer leaflet of a membrane?

A

Proteins in the membrane can quickly cleave the GPI-Protein bond to release the protein into the Extracellular space.

22
Q

3 movements that membrane proteins can exhibit

A

Rotational, Lateral movement, Conformational changes (transport proteins)

23
Q

Carbohydrates can only be found on which surface of the cell membrane?

A

Extracellular surface (Noncytoplasmic)

24
Q

Where and What is the Glycocalyx?

A

Located extracellularly. It is a carbohydrate-rich zone just off of the cell membrane.

25
Q

What enzymatic reaction is crucial to the formation of the glycocalyx?

A

Glycosylation

26
Q

What are the 3 main functions of the Glycocalyx?

A

Cell recognition, Cell signaling, and Water Absorption

27
Q

The glycocalyx of RBC’s determines

A

ABO blood types

28
Q

The 3 functions of glycocalyx in the intestines

A
  • Provides an additional surface that aids in absorption
  • Contains enzymes that aid in digesting macromolecules
  • Protects enterocytes from friction and digestive enzymes
29
Q

Lipid associated diseases (2)

A

Multiple Sclerosis and Niemann-Pick Disease

30
Q

Membrane Protein associated diseases (3)

A

Cystic Fibrosis, Duchenne, Muscular Dystrophy

31
Q

Glycosylation-related diseases (1)

A

Congenital disorders of Glycosylation

32
Q

Multiple Sclerosis

A

An autoimmune response that leads to the destruction of myelin producing cells. Demyelinated nerve cells struggle to transmit nerve signals.

33
Q

Niemann-Pick Disease: Types A and B

A

Sphingomyelinase deficiency leads to accumulation of sphingomyelin in the spleen, liver, lungs, bone marrow, and brain causing irreversible brain damage. Type A: Infants. Type B: Pre-teen.

34
Q

Cystic Fibrosis

A

Defective Cl- transporters in epithelial cells result in abnormally thick, sticky mucus that obstructs respiratory pathways.

35
Q

Congenital Disorders of Glycosylation (CDG)

A

Defects in the glycosylation pathway leads to abnormal glycocalyces (glycocalyx-es).