BIOL 4004 Exam 2

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Last updated 2:40 AM on 7/16/25
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300 Terms

1
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The ER lumen and golgi are topologically equivalent to the ________________

extracellular space

<p>extracellular space</p>
2
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the nucleus is continuous with the ___________

endoplasmic reticulum (ER)

3
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how many proteins is each nuclear pore complex (NPC) made up of

20-30 proteins

<p>20-30 proteins</p>
4
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the localization of T-antigen containing its normal nuclear import signal

T-antigen will be localized to the nucleus as normal

5
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localization of T-antigen containing a point mutation in the nuclear import signal

the sequence will no longer function as a NLS and the protein will remain in the cytosol

6
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T or F: the mitochondria is part of endomembrane communication and vesicular traffic

F

7
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All eukaryotic cells have the same basic set of _____1_____ that are functionally ______2______, and have __________3_________ compartments.

1. organelles

2. distinct

3. membrane-enclosed

8
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What did the evolution of internal membranes accompany?

the specialization of membrane function

9
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prokaryotes use their plasma membrane for ________

everything

10
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2 distinct evolutionary origins of organelles:

1. progressive formation of an endocytosis system

2. endosymbiotic relationship

11
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progressive formation of an endocytosis system

1. ancient prokaryotic cell

2. invagination

3. ancient eukaryotic cell

4. endomembrane system formation

12
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What 2 special functions did the cell membrane of the ancient prokaryotic cell have in the formation of the endocytosis system?

1. It could anchor the DNA

2. ribosomes attached to it (so protein synthesis could occur by membrane)

13
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endosymbiotic relationship

1. anaerobic pre-eukaryotic cell (from progressive formation of endocytosis system) engulfed an aerobic prokaryotic cell

2. initially both lived in symbiosis

3. aerobic eukaryotic cell with multiple mitochondria

14
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3 benefits of forming an aerobic eukaryotic cell

1. cell became more functionally independent

2. contains their own genome

3. nuclear compartment surrounded by a double membrane (protects the chromosomes)

15
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Where does protein synthesis begin?

on ribosomes in the cytosol

16
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sorting cells

direct protein delivery to specific locations from cytoplasm

17
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3 mechanisms used to move proteins from one compartment to another

1. gated transport

2. transmembrane transport

3. vesicle transport

18
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gated transport

movement of proteins into and out of the nucleus

<p>movement of proteins into and out of the nucleus</p>
19
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transmembrane transport

membrane bound protein translocates proteins across a membrane FROM the cytosol TO either the mitochondria or the ER lumen

20
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vesicle transport

membrane-enclosed transport vesicles move proteins between compartments

21
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example of vesicle transport

ER lumen --> golgi --> secretory vesicles --> cell exterior --> endosome --> lysosome (back into cell)

22
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2 amino acids that the nuclear localization signal (NLS) is rich in

1. Lys

2. Arg

23
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nuclear import receptor is a ___________ protein

cytoplasmic

24
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what does the nuclear import receptor bind

NLS and NPC proteins

25
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what does the nuclear import receptor have an affinity to

NPC

26
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nuclear export occurs in a similar/different way from nuclear import

similar

27
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2 things nuclear export requires

1. nuclear export signal

2. nuclear export receptors

28
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what provides directional transport through nuclear pore complexes

Ran GTPase

29
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T or F: nuclear transport is passive transport and requires no energy

F; it is active transport and requires energy

30
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process that provides energy for nuclear transport

energy is provided by the hydrolysis of GTP by Ran GTPase

31
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GTPase-activating proteins (GAPs)

triggers GTP hydrolysis and in effect inactivates Ran

32
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Guanine Exchange Factor (GEF)

promotes the exchange of GDP for GTP (exchange reaction) on Ran GTPase

33
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Ran-GTP binds to ____________________

nuclear import/export receptors

34
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Ran-GDP does not bind to ______________

nuclear import/export receptors

35
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Where is RanGDP localized?

cytosol

36
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Where is RanGTP localized?

nucleus

37
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Where is Ran-GAP located?

cytosol

38
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Where is Ran-GEF located?

anchored to chromatin and is therefore in the nucleus

39
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What drives nuclear transport in the appropriate direction?

the gradient of the two conformational forms of Ran

40
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Steps of nuclear import

1. Nuclear import receptor (R) binds to cargo

2. R/Cargo complex binds to NPC proteins

3. R/Cargo moves to nucleus side of NPC

4. Ran-GTP binds to R, releasing cargo

5. R/Ran-GTP is transported back through NPC to the cytosol

6. GTP is hydrolyzed by Ran-GAP

7. Ran-GDP dissociates from receptor

41
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Nuclear export occurs by a similar mechanism except that?

Ran-GTP (nucleus) promotes cargo binding to the export receptor

42
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Mitochondrial proteins are transported into the mitochondria (MT) by a _______-___________________ mechanism

post-translational

43
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what are mitochondrial proteins synthesized as?

as mitochondrial precursor proteins in the cytosol

44
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T or F: mitochondrial proteins do not require a signal sequence for transport

F: they do require a signal sequence

45
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How do mitochondrial proteins remain unfolded in the cytosol?

interact with chaperone proteins via binding

46
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What family of chaperone proteins do mitochondrial proteins interact with?

Hsp70 family

47
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____________________________ mediate protein transport across MT membranes

Protein translocators

48
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2 mitochondiral protein translocators

1. TOM complex

2. TIM complex

49
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TOM complex

translocase of the outer MT membrane

50
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TIM complex

translocase of the inner MT membrane

51
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T or F: the TIM complex can extend slightly into the outer membrane

T: this allows it to complex with TOM

<p>T: this allows it to complex with TOM</p>
52
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Steps of protein transport into mitochondria

1. precursor protein remains unfolded by binding Hsp70

2. signal sequence on N-terminus of protein binds to import receptor of TOM complex

3. translocation into matrix while still unfolded via binding of signal sequence to TIM complex

4. As soon as protein is in matrix, MT Hsp70 keep it unfolded until translocation is complete

5. signal sequence cleaved by signal peptidase

6. Hsp70 proteins leave and mature folded MT protein is formed

53
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What 2 things drives protein import in to the matrix space?

1. ATP hydrolysis

2. membrane potential

54
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Protein import into the mitochondria (MT) requires energy at what 3 steps?

1. ATP hydrolysis in the cytosol

2. Electrical H+ gradient (generated by H+ from the matrix to the intermembrane space)

3. ATP hydrolysis in the matrix space

<p>1. ATP hydrolysis in the cytosol</p><p>2. Electrical H+ gradient (generated by H+ from the matrix to the intermembrane space)</p><p>3. ATP hydrolysis in the matrix space</p>
55
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5 vital cellular functions of ER

1. Protein synthesis and sorting

2. lipid biosynthesis

3. glycolsylation

4. attachment of lipid anchors to proteins

5. intracellular storage of calcium ion

56
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glycolsylation

- attachment of sugars to proteins

- forms glycoproteins

57
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Where does lipid modification occur?

golgi

58
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T or F: ER is a closed vesicular space

T

59
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transmembrane proteins end up going to the __________

membrane

60
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secreted proteins end up _________________?

being secreted outside of the cell

61
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proteins can be destined for the lumen of the ER and other organelles such as ______1______ and ______2_____

1. golgi

2. lysosome

62
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import of proteins into the ER lumen is a ____-____________________ process

co-translational process

63
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T or F: import of proteins into ER requires chaperone proteins

F: no, because this transport is co-translational

64
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T or F: Import of proteins into ER lumen requires additional energy

F

65
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Where does the translation of all proteins start?

cytosol (from there it can be directed to the mitochondria or ER lumen, etc)

66
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Signal recognition particle (SRP)

directs ER signal sequences to a specific receptor in the rough ER membrane

67
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the ER signal sequence is highly hydrophillic/hydrophobic (1) because of its _____-_____ (2) nonpolar amino acid stretch

1. hydrophobic

2. 15-20

68
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Steps of protein translocation to rough ER membrane

1. translation starts in cytosol

2. SRP binds to signal sequence and ribosome blocking translation

3. SRP-ribosome complex binds to SRP receptor in ER membrane

4. SRP-ribosome complex binds to protein translocator

5. re-initiation of translation

69
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model for translocation of a soluble protein across the ER membrane

1. re-initiation of translation

2. co-translational insertion into ER lumen

3. translation "pushes" polypeptide into ER

4. growing polypeptide forms a loop

5. ribosome is released after translation is finished

6. signal sequence is cleaved by signal peptidase

7. mature folded protein

70
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model for insertion of a single-pass transmembrane protein into the ER membrane

1. signal sequence serves as a start-transfer signal

2. hydrophobic stretch of amino acids in polypeptides acts as a stop-transfer signal

3. stop-transfer signal anchors protein into the membrane (does not stop translocation)

4. stop-transfer signal is released into the membrane by the translocator and becomes membrane spanning segment of membrane

71
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What is different about the transmembrane protein utilized for single-pass insertion into the ER membrane?

there is an additional hydrophobic region on the peptide that is NOT the signal sequence

72
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What happens when you have multiple pairs of start and stop sequences?

you can use multiple translocators at the same time and have multiple transmembrane domains

73
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multiple start/stop-transfer signals direct each TM sequence into the ____1_____ and each region will be inserted into the ____2____ membrane

1. translocator

2. ER

<p>1. translocator</p><p>2. ER</p>
74
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What are most proteins in the ER?

glycoproteins

75
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preformed precurser oligosaccharides

made in the ER but not linked to translation, there is always a pool of them

76
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preformed precursor oligosaccharides are transferred to what?

proteins

77
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dolichol

lipid molecule that holds the precursor oligosaccharide in the ER membrane

78
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the precursor oligosaccharide is transferred to what amino acid residues?

Asn (N)

79
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oligosaccharyl transferase

Enzyme that transfers a precursor oligosaccharide from membrane-bound dolichol to certain N residues of proteins imported into the ER.

<p>Enzyme that transfers a precursor oligosaccharide from membrane-bound dolichol to certain N residues of proteins imported into the ER.</p>
80
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consensus sequence for N-linked glycosylation

N-X-S/T

81
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Where are most membrane lipid bilayers assembled?

ER

82
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What does the ER membrane synthesize?

most of the major classes of lipids

83
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where does the synthesis of phospholipids occur?

exclusively in the cytosolic leaflet of the ER membrane

84
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Scramblase

phospholipid translocator that equilibrates between 2 leaflets

<p>phospholipid translocator that equilibrates between 2 leaflets</p>
85
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transport vesicles

transfer lipids and proteins between some organelles

86
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5 organelles that transport vesicles work between

1. plasma membrane

2. ER

3. golgi

4. lysosomes

5. endosomes

87
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microsomes

- artificial organelles derived from the ER (not naturally in mammalian cells)

- fragments of ER but still functional (can do everything ER can do)

88
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Microsome formation

Cells are homogenized (crushed) making cells unviable, but still leaving some organelle function

89
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In vitro-translation without microsomes

ribosomes are isolated and translation occurs without microsomes

<p>ribosomes are isolated and translation occurs without microsomes</p>
90
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In vitro translation with microsomes

knowt flashcard image
91
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What happens when you add a small amount of protease to experiment with in vitro translation without microsomes?

the proteins will be degraded since there is no protection by a membrane

92
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What happens when you add secreted mRNA to experiment of in vitro translation with microsomes?

mRNA will be translated on the ribosome on the microsome and the translated proteins will end up on the lumen side of the microsome

93
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What happens when you add a small amount of protease to experiment with in vitro translation with microsomes?

it will degrade the protein outside of the ER membrane but the protein below the membrane will be protected

94
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What happens when you add detergent and protease to experiment with in vitro translation with microsomes?

detergent will disrupt the microsome membrane allowing entire protein to be susceptible to degradation

95
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What happens when you run a gel with the same polypeptides from the experiment of in vitro translation without microsomes?

there will be one band because the protein segments will be the same size (no modifications)

96
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What happens when you run a gel with the same polypeptides from the experiment of in vitro translation with microsomes?

there will be multiple segments (ladder) because signal sequences could be cleaved and sugars could be added on via microsome method

97
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1 out of 500 individuals has one defective _______1______ R which gives them a high risk of heart attack by ___________2___________

1. LDL

2. atherosclerosis

98
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transport vesicles ______ 1________ from one compartment and ____2___ with another

1. bud off

2. fuse

99
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what do transport vesicles carry?

materials as cargo

100
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2 major pathways utilized by transport vesicles

1. biosynthetic secretory pathway

2. endocytic pathway