2. Nucleic Acids Flashcards

1
Q

What are the components of a nucleotide

A
  • sugar
  • phosphate
  • nitrogen bases
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2
Q

Draw and label the donor and accpetor in the nitrogen bases

A
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3
Q

Draw Uracil and compare it to thymine

A
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4
Q

where are the nitrogenbases attached to the sugar?

A
  • N1 in pyrimidines
  • N9 in purines
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5
Q

How to differinatiate DNA and RNA by the sugar base

A
  • OH group on C2
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6
Q

Draw a sugar and label the carbons

label chirality

A
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7
Q

How to name nucelosides (base + sugar)

A
  1. pruines uses osine as a suffix
  2. pyrimidines become idine as a suffix
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8
Q

label the differnces of phosphodiester, phosphoester and phosphanhyride bonds within a dinucleotide structure

A
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9
Q

What is the overall net charge of the nucleotide, is the back bone polar or non-polar? and compare the backbone of RNA and DNA, which is more polar?

A
  • net charger = more negative largely consistent within the strucutre (cause of phosphate groups)
  • sugar is polar and the phosphate is more polar
  • backbone in RNA vs DNA = RNA is more polar
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10
Q

explain spontanous, alkaline hydrolysis of phosphodiester bonds in RNA

A
  • 2 products are fromed:
  • a free nucleotide
  • and a nucleotide with phosphate group attachment
  • in DNA the absense of the OH group prevents this reaction, making it more stable than RNA in alkaline conditions
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11
Q

Explain the deamination of cytosine to uracil

A
  • spontaneous (uncatalyzed) reaction
  • uncorrected in DNA can cause a mutation
  • DNA repair mechanisma will reocgnize U and remove it
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12
Q

what is a dideoxynucleotide

A
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13
Q

Explain the properties of the bases

A
  • heterocyclic
  • aromatic with elctron delocalization
  • basically planar
  • poorly soluble
  • largely hydrophobic with some polar groups (abilit to form H-bonds)
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14
Q

Explain absorbance

how to measure pure DNA, what is used to measure concentration

A
  • A260nm/280nm = 1.95 for pure DNA
  • contamination lowers the ratio
  • protein abs maxi at 280nm
  • DNA abs is about 50% at 280 nm
  • A260nm is used to meaure the concentration of nucleic acids in solution
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15
Q

Draw the hydrogen bonding between the nucleotides in DNA

A
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16
Q

What is DNA (B-form) and describe the characteristics

A
  • stablized by base stacking interactions and H-bond but base stacking is the primary force
  • base stacking: primarily van der wasl forces and hydrophobic forces
  • has an overall right handed twist
  • ~10bp per turn
17
Q

Explain the denaturation of DNA

A
  • separation of the two paried stranded ds -> ss
  • disruption of non-covalent forces (H-bonds and base stacking)
  • essential for some cellular processes
  • changes in absorption properties; increase at 260nm as the strands separate
18
Q

What does DNA melting (denaturating) look like on a graph

Label Tm

A
  • Absorbance increases as temp increases
  • Tm = midpoint of melting with comprise of dsDNA and ssDNA 50;50
19
Q

Define hyperchromicity and hypochromicity

A
  • hyper = is a relatively high abosrbance
  • hypo = is a low absorbance
20
Q

Explain DNA zippering

A
  • theres a fast zippering
  • slow rate depends on the complexity of the necleic acid = nucleatio; eg. its like the slow step of alinging the zipper before it zips properly
21
Q

Explain the relationship b/w Tm and the GC content of a DNA

A
  • as GC content increases so does Tm
  • GC bairs have stronger base stackng interactions than AT pairs
22
Q

What can affect Tm?

A
  • changing PH: affects protonation state of DNA; but a bell curve
  • changing slat concentrations; increase causes more stabilization as there are less repulsions on the phosphate backbone; increase salt -> increase Tm; decrease salth -> decrease in Tm
  • Tm of hybridization; more identical = an increase in Tm
23
Q

What is the differnce in DNA and RNA structures

define : inter and intrastrand base pairing

A
  • RNA has intrastrand base pairing; DNA has interstrand
  • strucutre of RNA is much more dependent on nucleotide sequecence thn double-stranded DNA