Cell 1 Flashcards

(41 cards)

1
Q

What does the plasma membrane consist of and what %’s?

A

50% protein

45% lipid

5% carbohydrates

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1
Q

What is a method of membrane cleavage?

What are the 2 sides of the membrane called?

To which side do most membrane particles remain attached to?

A

Cryofracture (freeze fracture)

Protoplasmic face (P) and Extracellular face (E)

P

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1
Q

What are the 3 functions of peroxisomes?

A
  1. Oxidize organic substances by transferring H atoms to molecular oxygen
  2. The product hydrogen peroxide is toxic and removed by catalase, which is inside the peroxisome
  3. Beta oxidize long chain and branched fatty acids
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2
Q

Describe the steps of Receptor-Mediated endocytosis

A
  1. Binding of ligands to receptors causes receptors to accumlate in coated pits coated by clathrin
  2. The coated pit invaginates and pinches off forming a coated vescicle containing the receptor & bound ligand
  3. Coated vescicles lose their clathrin and fuse w/ endosomes. Clathrin detaches and recycles back to PM
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2
Q

How do new mitochondria arise?

A

By fission of existing mitochondrias

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2
Q

What subunits do eukaryotic ribosomes consist of?

Where is RNA synthesized in eukaryotic cells?

A

60S and 40S.

in the nucleus

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2
Q

What does the SER do in muscle cells

A

It participates in contraction. Here it is called the sarcoplasmic reticulum is involved in the sequestration/release of ca2+ during contraction

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3
Q

What is the cytoskeleton composed of?

What is its function?

A

Microtubules, microfilaments, and intermediate filaments.

It provides shape and allows movement of cells

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4
Q

What is the unit membrane composed of?

A

An electron lucent layer b/w 2 electron dense layers

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6
Q

How are the proteins of the PM made?

A

They are SYNTHESIZED in the Rough ER, MODIFIED in the Golgi, and transferred to the cell membrane

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7
Q

What is the thickness of the Plasma Membrane?

A

7.5-10nm

visible by EM

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7
Q

What do ribosomes bind to in the ER?

A

A signal recognition particle (SRP)

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7
Q

In what direction in the golgi are vesicles transported?

A

Convex Cis face (close to RER) TO concave trans face

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8
Q

What happens to the PM vesicles that invaginate due to pinocytosis?

A

They eventually fuse with lysosomes

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9
Q

What are the 3 types of movement of molecules through the PM?

A

Simple diffusion,

Carrier protein,

Channel protein

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11
Q

The rough ER does what?

A

It segregates proteins NOT destined for the cytosol

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13
Q

What is the environmenet inside lysosomes?

Where are lysosomes abundant?

A

Internally acidic, containing hydrolytic enzymes.

Abundant in phagocytic cells like macrophages

14
Q

What is actin important for?

A

Motility, shape, and movement of organelles

15
Q

What are special about endosomal membranes? What does this cause?

A

They contain ATP-driven proton pumps which acidify the interior compartment.

This causes the separation of ligand/receptor complexes, allowing receptors to cycle back to PM

17
Q

How many types of cells are there in humans?

17
Q

Where are lysosomal membranes/proteins packaged?

How are they delivered?

A

In the TRANS-Golgi network.

They are delivered separately in clathrin-coated vesicles to late endosomes forming endolysosomes which mature to become lysosomes.

18
Q

What are the 4 types of integral membrane proteins?

A
  1. Transport proteins (eg Na, K, and ATPase)
  2. Ion selective channels
  3. Receptors
  4. Anchoring structural proteins
19
Q

What are zymogen granules?

A

Membrane bound vesicles containing digestive enzymes

21
Q

What is the glycocalyx?

What charge is it and why?

A

A cell surface coat consisting of externally exposed oligosaccharide chains from proteins and lipids.

The glycocalyx has a negative charge due to the presence of carboxyl groups and sulfate ions.

22
What are proteasomes?
They romove excess and improperly folded proteins
23
Intermediate filaments are composed of several proteins 10-12nm in diameter. Name one.
Keratin Vimentin Desmin GFAP Neurofilaments
24
What is special about the mRNA of proteins that are destined for the ER?
They have a 20-25 HYDROPHOBIC sequence of amino acids that signals for protein translocation through the ER
25
What do ribosomes consist of?
4 diff types of RNA and \>80 proteins
26
What is characteristic of primay cilia?
1. Ubiquitous, 2. Non-motile and very small, 3. Serve as Sensory receptors, 4. 9+0 arrangment of tubulin dimers
27
Where are the components of ETC and oxidative phosphorylation associated in the Mitochondria?
The IMM
29
What is the arrangement of each centriole? When does the CENTROSOME duplicate?
9+3 CENTROSOME duplicates before cell division in S phase
30
What is the diff b/w primary and secondary lysosomes?
Primary aren't involved in digestion, secondary are fused with a phagosome
31
How does cholesterol affect the PM?
Cholesterol increases the fluidity of the PM by disrupting the packing of long phospholipid fatty acid chains
33
What are the Smooth ER specialized functions?
Synthesis of steroid hormones and phospholipids
34
What are auto/heterophagosomes? What are their end products?
Autophagosomes is a fusion of a phagosome and lysosome w/ intracellular organelles. Heterophagosome is a fusion of a phagosome and lysosome w/ foreign materials. Their end product is a yellow pigment which accumulates w/ age AKA lipofuscin
35
What are microtubules? They form the basis for which cytoplasmic structures?
cylindrical tubes of heterodimers composed of alpha and beta tubulin. 1)Centrioles, 2)basal bodies, 3)primary cilia, 4)cilia, 5)flagella.
37
What is the ration of proteins to lipids in Mitochondrial membranes?
High protein to lipid ratio
38
What is the core organization arrangement for cilia and flagella? How does nexin and dynein play a role? What is at the base of each cilia/flagellum?
9+2. Nexin links microtubule pairs, dynein extends out (it is an ATPase). At the base is a basal body which consists of microtubules arranged as a centriole
39
What are cristae in mitochondria and what is their purpose?
They are folds in the Inner Mitochondrial Membrane that increase the Surface Area of the IMM.
40
What does the Golgi Apparatus do?
It completes the post-translational modification of proteins
41
What is the fluid mosaic model of the membrane?
A DYNAMIC model in which proteins can move LATERALLY. Lipids can also move rapidly W/IN the monolayer and slower B/W monolayers