Week 1 - Structure and Properties of Nucleic Acids Flashcards
bases in nucleic acids
- attached to 1’C sugar
purines have two bases:
- adenine
- guanine
pyrimidines have three bases:
- cytosine
- thymine
- guanine
nucleotide charge
negative
primary structure of nucleic acids
base stacking
base stacking
- bases stack on top of each other
- interactions result from hydrophobic effect
phosphodiester bonds
joins sequence of nucleotides
secondary structure of nucleic acids
pentoses have a puckered conformation
- either C-2’ or C-3’ can be puckered
- puckered can be endo (towards 5’C) or exo (away 5’C)
key features of secondary structure of double stranded nucleic acids
- two nucleic acid molecules
- anti-parallel
- helical
- complementary
common hydrogen bonding patterns in DNA
- adenine bonded to thymine (1 pi bond)
- guanine bonded to cytosine (2 pi bonds)
different helical structures in double stranded nucleic acids
precise atomic positions can differ due to:
- sugar pucker
- rotation around bonds in nucleotides
rotation around 7 bonds in double helix
- theoretically, 1, 2, 3, 5, and 6 have free rotation
- 4 (delta) belongs in a sugar ring, therefore rotation is harder
- 7 (chi) is near a bulky base, therefore rotation is restricted
purine conformations
- anti-adenosine is the normal conformation
- syn-adenosine is a possible conformer but rarer
pyrimidine conformations
only anti-cytidine is possible as the =O causes steric hindrance
forms of helical double stranded nucleic acids
- a form
- b form
- z form
A form
- helical: right handed
- bp per helical turn: 11
- length: 2.6 A
- base tilt: 20 degrees
- sugar pucker: C-3’ endo
- glycosidic bond: anti
B form
- helical: right handed
- bp per helical turn: 10.5
- length: 3.4 A
- base tilt: 6 degrees
- sugar pucker: C-2’ endo
- glycosidic bond: anti