Biol 213 ch. 15, 16, 17, 18 Flashcards

1
Q

what creates enclosed compartments that segregate different metabolic processes

A

internal membranes

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2
Q

what is the nucleus surrounded by?

A

a double membrane (nuclear envelope)

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3
Q

how does the nucleus communicate with the cytosol?

A

via nuclear pores that perforate the envelope

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4
Q

cytosol function

A

-contains metabolic pathways
-protein synthesis
-cytoskeleton

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5
Q

nucleus function

A

-contains main genome
-DNA and RNA synthesis

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6
Q

Smooth ER function

A

-lacks ribosomes
-site of steroid hormone synthesis in adrenal gland
-site where a variety of organic molecules (like alc) are detoxified in liver cells

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7
Q

Rough ER function

A

synthesis of most lipids

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8
Q

Golgi Apparatus function

A

-modification, sorting, and packaging of proteins and lipids for either secretion or delivery to another organelles

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9
Q

lysosomes function

A
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10
Q

endosomes function

A

sorting of endocytosed material and recycle some back to membrane

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11
Q

mitochondria main function

A

ATP synthesis by oxidative phosphorylation

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12
Q

chloroplasts function

A

ATP synthesis and carbon fixation by photosynthesis

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13
Q

peroxisomes function

A

-packed with enzymes that digest toxins and synthesize certain phospholipids
-oxidative breakdown of toxic molecules
-produce H2O2

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13
Q

what do cytoskeletal filaments do?

A

-provide tracks for moving the organelles around
-direct traffic of vesicles between 1 organelle and another

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14
Q

how did mitochondria and chloroplasts evolve?

A

aerobic bacterium was engulfed by a larger anaerobic eukaryotic cell

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15
Q

what determines protein synthesis?

A

amino acid sequnce

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16
Q

what does signal sequence/ sorting signal do?

A

directs proteins to organelles where they are required

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17
Q

what happens to proteins without sorting signals?

A

remain in cytosol

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18
Q

how do molecules go from cytosol to nucleus?

A

nuclear pores

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19
Q

what are nuclear pores?

A

selective gates that actively transport specific macromolecules (but also allow free diffusion of smaller molecules)

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20
Q

how do molecules enter mitochondria/chloroplasts?

A

transported by protein translocators
-transported protein must unfold for translocator to guide it across hydrophobic interior
-signal sequence is removed after translocation is complete

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21
Q

how do molecules go from ER (EMS) go anywhere?

A

transport vesicles that pinch off membrane of 1 compartment and fuse with membrane of a second compartment

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22
Q

what is the nuclear lamina?

A

meshwork of protein filaments that lines the inner face of inner membrane and provides structural support for nuclear envelope

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23
Q

what does the nuclear envelope do?

A

encloses the nuclear DNA and defines the nuclear compartments

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24
Q

what are desmosomes

A

cell-cell junctions where the plasma membrane is connected to that of another cell

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25
Q

nuclear lamina

A

underlies and strengthens the nuclear envelope

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26
Q

what is in the inner nuclear membrane

A

-proteins thata act as binding sites for chromosoems
-proteins that provide anchorage for nuclear lamina

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27
Q

what drives nuclear transport?

A

energy supplied by GTP hydrolysis

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28
Q

what does Ran-GAP do?

A

turns GTP into GDP
-activates GTPase

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29
Q

what do chaperone proteins do?

A

help pull protein across membranes and fold once it is inside

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30
Q

what is the only organelle that serves as an entry point for proteins destined for other organelles

A

ER

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31
Q

where do proteins that are destined for Golgi Apparatus, endosomes, lysosomes, and those destined for cell surface first go?

A

ER. From then on they will be transported by vesicles

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32
Q

what kinds of proteins are transferred from cytosol to ER?

A

1) water-soluble- destined for secretion or lumen in an organelle in EMS
2) prospective transmembrane- destined to reside in membrane of EMS organelles or plasma membrane

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33
Q

what signal sequence directs protiens to ER?

A

8+ hydrophobic amino acid

34
Q

what are the 2 types of ribosomes in the cytosol and what are their functions?

A

1) membrane-bound- make proteins destined for ER
2) free ribosomes- make proteins encoded by DNA

34
Q

what are the 2 types of ribosomes in the cytosol and what are their functions?

A

1) membrane-bound- make proteins destined for ER
2) free ribosomes- make proteins encoded by DNA

35
Q

what end of polypeptide chain must pass through translocator for protein to be released into ER lumen?

A

C terminus of growing polypeptide chain

36
Q

how do proteins get to ER membrane?

A

SRP binds to exposed ER sequence

37
Q

outward secretory pathway

A

proteins are transported form ER through Golgi apparatus to plasma membrane

38
Q

how do components travel through the Golgi Apparatus>

A

via vesicles that shuttle between its individual cisternae

39
Q

what are protein coat functions?

A

1) shape membrane into a bud
2) capture molecules for onward transport`

40
Q

what do clathrin molecules do?

A

form basketlike cages that help shape membranes into vesicles

41
Q

what do clathrin-coated vesicles do?

A

1)Golgi to lysosome (via endosome)
2) plasma membrane to endosomes

42
Q

what do adaptins do?

A

secure clathrin coat to vesicle membrane and help some cargo molecules for transport
-bind cargo receptors in Golgi App.
-bond cargo receptors in plasma membrane

44
Q

what do dynamin proteins do?

A

assemble around the neck of a budding vesicle, hydrolyze GTP, and pinch off vesicles

45
Q

what provides initial recognition between vesicle and target membrane?

A

Rab and tehtering proteins

46
Q

what are SNARE proteins?

A

transmembrane proteins that provide addiitional recognition in ensuring transport vesicles dock at appropriate target membranes

47
Q

what serves as molecular markers for each membrane type?

A

Rab proteins

48
Q

what do disulfide bonds do?

A

stabilize structure of proteins that will encounter degradative enzymes and changes in pH outside cell

49
Q

why don’t disulfide bonds form in cytosol?

A

the environment in cytosol is reducing

50
Q

what do oligosaccharides do?

A
  • protect a protein from degradation
    -hold protein in ER until it is properly folded
    -form cell’s outer carb layer (glycocalyx)
51
Q

what is the ER retention signal?

A

C-terminal sequence of 4 a.a.

52
Q

what is the difference between cis and trans sides of Golgi App

A

cis: adjacent to ER
trans: points towards plasma membrane where proteins exit

53
Q

what are endosomes?

A

where ingested materials go
-there, ingested materials are recycled to plasma membrane or sent to lysosomes for digestion

54
Q

what do phagocytic cells do?

A

-ingest large particles
-defend against infection by ingesting invading microorganisms
-scavenge dead and damaged cells

55
Q

what are macrophages?

A

-a type of phagocytic cell found in tissues and other WBC

56
Q

how do macrophages engulf bacterium?

A

particles bind to surface receptors, which induces phagocytic cell to extend sheet-like projections of plasma membrane (pseudopods) that engulf bacterium and fuse their tips to form phagosome

57
Q

what do phagosomes do?

A

fuse with lysosomes, where microbes are destroyed

58
Q

what is pinocytosis?

A

cell ingestion of their plasma membrane
-cells SA and vol. dont change -> equal rates of endo and exocytosis
-carried out mainly by clathrin-coated vesicles

59
Q

cholesterol

A

-extremely insoluble lipid in water
-transported in bloodstream in the form of low-density lipoproteins (LDL), which enters cell via
receptor- mediated endocytosis

60
Q

where are early endosomes?

A

just beneath plasma membrane
-matura gradually into late endosomes as they fuse w each other

61
Q

where are late endosomes?

A

located closed to nucleus

62
Q

how does the endosome stay acidic?

A

by ATP-driven H+ pump in endosomal membrane that pumps h+ into endosome lumen from cytosol

63
Q

how do proteins stay from getting digested by the lysosomal proteases?

A

sugars (glycosylated)
proteases, nucleases, proteases, lipases, phosphatases, sulfatases, phospholipases

64
Q

what is the function of the cell cycle?

A

duplicate DNA in chromosomes and segregate DNA into genetically identical daughter cells

65
Q

why doesn’t the cell grow in M phase?

A

cannot produce new proteines in that phase because it is in heterochromatin (super coiled)
-so it can’t be transcribed and therefore no mRNA synthesis

66
Q

What are the checkpoints?

A

after G1: checks if environment is favorable (sufficient nutrients, specific signal molecules)
after G2: checks DNA is undamaged and fully replicated
after M: before chromosomes are pulled apart, checks duplicated chromosomes are properly attached and aligned on mitotic spindle

67
Q

what do kinases do?

A

phosphorylate

68
Q

what do phosphatases do?

A

perform dephosphorylation

69
Q

what do cyclins do?

A

turn kinases on and off

70
Q

what are Cdks?

A

cyclin-dependent protein kinases of the cell control system
-only activate once bound to cyclin

71
Q

why is increase in cyclin concentration gradual?

A

because of continued transcription of cyclin genes and synthesis of cyclin proteins

72
Q

what is fall in cyclin concentratation rapid?

A

full scale targeted destruction of the protein by APC/C

73
Q

what drives the removal of M cyclin at the end of mitosis?

A

1) activation of APC/C
2) APC/C tags cyclin with ubiquitin
3) cyclin gets taken away to proteasomes

74
Q

what does APC/C stand for?

A

anaphase promoting complex

75
Q

what triggers the rapid activation of M-cdk?

A

phosphatase (cdc 25) removes inhibitory phosphates that inhibitory kinase put

76
Q

what is p27?

A

an inhibitory protein that inactivates Cdks and cell can’t progress through G1 into S phase

77
Q

what are the mechanisms in the cell-cycle that pause the cycle at specific points?

A

after G1: Cdk inhibitors block entry to S phase and replication of DNA
after G2: inhibition of activating phosphastase (Cdc25) supressess activation of M-Cdk
after M: inhibition of APC/C activation, preventing degradation of M cyclin

78
Q

what happens in G1 phase?

A

DNA is made replication-ready by recruitment of proteins to origins of replication
-Cdks are inactivated

79
Q

what do mitogens do and what happens if a cell is deprived of them?

A

mitogens are extracellular signals/stimuli that tell cells to grow
-if deprived, cell cycle arrests in G1

80
Q

how does a cell escape cell-cycle arrest?

A

buildup of cyclins triggers G1/S- Cdk activity, which relieves the negative controls that otherwise block progression from G1 to S phase

81
Q

What is the Rb protein?

A

Retinoblastoma
-inhibiti

82
Q

What is the Rb protein?

A

Retinoblastoma
-inhibiti

82
Q

What is the Rb protein?

A

Retinoblastoma
-inhibiti