Exam 3 Weekly project and slides Flashcards

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1
Q

methicillin

A

beta-lactam antibiotic => inhibits the formation of the peptidoglycan layer of the cell wall in bacteria and can also kill good bacteria in our gut

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2
Q

how to bacteria develop resistance to methicillin

A

they acquire genes that encode proteins that don’t bind to methicillin and prevent it from killing the organism=> eukaryotes don’t have peptidoglycan walls so they are safe

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3
Q

clotrimazole

A

fungal cell with large holes in it that form due to the drug inhibiting an enzyme that catalyzes ergosterol synthesis in fungal cells (cant construct a functioning membrane)

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4
Q

how clotrimazole is safe

A

ergosterol is only found in fungi cell membranes not animal cells so they are left unharmed ==> we have cholesterol instead

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5
Q

raltegravir

A

antiretroviral integrase stand transfer inhibitor that inhibits the pre-integration complex by binding to magnesium in the integrase enzyme => decreases HIV in the blood

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6
Q

why raltegravir is safe for humans

A

mostly targets integrase in HIV compared to other transferases such as human cells

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7
Q

azithromycin

A

antibiotic that inhibits the 23S rRNA in the 50S subunit in protein synthesis for ribosomes => permeates the cell membrane and breaks through the glycocalyx

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8
Q

why is azithromycin safe?

A

only targets prokaryotic ribosomes instead of eukaryotic ones so human cells are unaffeced

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9
Q

exemestane

A

goes after aromatase enzyme so it cannot produce estrogen and keeps it as testosterone => no aromaticity and treats breast cancer or other cancers involving estrogen production (hormone sensitive tumors)

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10
Q

side effects and diseases treated by exemestane

A

lower estrogen => hot flashes, developmental issues, flushing, loss of period, headaches, etc. and causes testosterone to increase leading to acne, hair loss, and infertility

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11
Q

why is exemestane not used in pre-menopausal women

A

prevents puberty and wouldn’t work because most cancers rely on all estrogens instead of only testosterone being converted to estrogen

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12
Q

taxol

A

interferes with microtubule functions in some cancer treatments => actin helps maintain cell structure and a breakdown of it causes cells to lose shape and loss of function like signaling, mobility, and division => nonspecific and target all cells in the body causing side effects and inability to replicate

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13
Q

If mena is deleted, how is Lpd affected?

A

lamellipodin remains localized on the leading edge still which tells us it plays a role in the movement of it

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14
Q

if LPD is deleted, how is mena affected?

A

mena would not be localized at the leading edge because it couldn’t bind to Lpd

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15
Q

how to make a fusion protein

A
  1. cut gene sequences out of fibroblast cell with restriction enzymes correlating to each gene segment
  2. optional: use PCR to amplify each gene sequence
  3. ligate each gene sequence together after they are mixed and hydrogen bonded
  4. ligate gene back into the plasmid vector
  5. get bacteria to take up plasmid with antibiotic solution
  6. bacteria transcribes gene over and over again
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16
Q

which is the control fusion protein. D or E?

A

HELP

17
Q

how can you test if mena and Lpd bind together directly?

A
  1. put the plasma/gene in a bacteria culture and make copies of each of the proteins separately
  2. purify the proteins from the solutions
  3. put the two proteins in a solution and immunoprecipitate them so that would allow them to make a complex like in a cell
  4. perform a Co-IP to see if the proteins formed the complex as we predicted
18
Q

what happens?

A

Will undergo apoptosis due to continued flipping of inner leaflet

19
Q

Intracellular Na and ATP but no extracellular K+ what conformation state?

A

the pump would be stuck facing outward with no K+ to trigger the inward movement back into the cell. The inside of the cell would be positive and unable to return to resting state

20
Q

differences between channels and pumps

A
  1. channels only go one way with gradient and pumps go against gradient
  2. pumps are antiporters (2 different molecules) while channels are uniporters (1 molecule)
  3. channels use passive facilitation vs pumps use active transport
21
Q

if Na/K+ pump is working and the Na+ channel is open at the same time what happens?

A

Na+ would constantly be entering the cell and exiting the cell (via the pump) at the same time but K+ would only be pumped back into the cell against the gradient => the internal of the cell would constantly be positive and it wouldn’t be able to fire a new action potential because it wouldn’t return to resting state

22
Q

how do channels regulate their ions?

A

voltage gated (electrical signals) via charge distributions in and outside the cell (Sodium and potassium internally) and chemical signals triggered by concentration gradients wanting to be in equilibrium

23
Q

how does living in salt water affect fishes cells?

A

water wants to constantly diffuse out of the cell to find isotonicity

24
Q

why do fish drink salt water in the ocean and excrete excess salt?

A
  1. to make sure their cells don’t shrivel due to osmolarity and water diffusing out of the cell
  2. to keep salt concentrations lower in their external cellular environments to prevent osmosis diffusion
25
Q

active or passive transport for H+ and Pi?

A

–> active for Pi
–> passive for H+

26
Q

if a plant wants to transport phosphate into the cell why does it coordinate with H+?

A

the H+ passive gradient allows the phosphate to be actively transported without the use of energy because H+ is already moving in that direction

27
Q
A
28
Q

T/F the PHS transporter is responsible for establishing the H+ and/or Pi gradient?

A

True for Pi but false for H+. H+ is getting pumped out of the cell via a different pump such as NADH

29
Q

4 compartments of a eukaryote

A

cytosol, nucleus, endomembrane system, semiautonomous organelles

30
Q

cytosol

A

ribosomes, cytoskeleton, centromeres (centrioles)

31
Q

nucleus

A

nucleolus, nuclear matrix, nuclear pores, chromatin/chromosomes

32
Q

endomembrane system

A

plasma membrane, nuclear envelope, RER, SER, golgi, vesicles, vacuoles, lysosomes, peroxisomes

33
Q

semiautonomous

A

mitochondria and chloroplasts

34
Q
A