BB7 Structures From NMR Flashcards
Nuclei with intrinsic magnetism
- 1-H
- 13-C
- 15-N
- 31-P
Nuclear Magnetic Resonance (NMR)
• reveal atomic structures of macromolecules IN SOLUTION
1-H can be used in NMR to see the structures of
proteins
• extensively found in biological systems
31-P is used in NMR to study the structures of
nucleic acids
NOT PROTEINS
The magnetism of nuclei comes from
the SPIN of their protons
The spin of 1-H generates a
magnetic moment
In an applied magnetic field, magnetic moment adopts 1 of 2 orientations
- α = orientated WITH the field
* β = orientated AGAINST the field
B0 (sub)
applied magnetic field strength
Delta E
- energy difference between α and β
- proportional to B0
- in the radio frequency range
1-H nuclei in the α state can be excited into the β state
• requires pulse input of radio-frequency energy
Pulse input - radio frequency
ν0 = γH0 / 2π
- ν0 = radio-frequency
- γ = magnetic ratio for a given nucleus
Electrons around 1H
- alter the magnetism that the nucleus experiences
- creates a local chemical environment
- shields protons from the applied field
Electrons shield protons from the applied field
H0 = B0 (1 - σ)
- H0 = local magnetic field strength
- σ = shielding factor (modifying agent)
1H nuclei in different chemical environments will have different
ν0 values
• very small
• scaled as δ - ppm
The local magnetic field is further altered through
- molecular bonds to neighboring nuclei with magnetic moments
- nuclei affect each other = spin-spin coupling
Spin-spin coupling requirements
- neighboring nuclei must be in different chemical environments (even for seemingly identical groups)
- nuclei must be 3 or less bonds apart (otherwise too small to be seen)
Relaxation
nuclei excited to the β state must lose energy to return to the α state
• occurs via interactions with other near neighbour magnetic nuclei
An NRM spectrum is the observation of
β state protons falling back to the α state
2 forms of relaxation
- relaxation through bonds
* relaxation through space
Relaxation can also be observed by
• 2-D NMR spectroscopy
2-D NRM spectroscopy
- . spectra are drawn as a 2-D contour map of peaks
- peaks on the diagonal are the 1-D NMR spectra
- peaks off the diagonal show where relaxation interactions have occurred
2-D correlation spectroscopy (COSY)
- gives structural info through bond connections between residues
- identifies the residues
2-D nuclear overhauser spectroscopy (NOESY)
- through space or bond effect
- reveals info about structure through space relaxation interactions
- uses Nuclear Overhauser Effect (NOE) data
- peaks on diagonal spectrum are a normal 1-D spectrum
- used as markers to locate the off-diagonal peaks
- 1H nuclei close space to each other will share an off-diagonal peak (symmetric in appearance)
- off-diagonal peaks shower where relaxation has occurred between 1H nuclei through space
- large number of off-diagonal peaks are present in a 2-D spectrum (represent nuclei in close proximity to each other)
Ensemble of structures
NOESY together with additional data obtainable from an NMR , a SET of solution conformation of a protein can be obtained
• near terminal
• through bond effects, not space
• side chains on extremes, floppy
Potential problems of NOESY
- no SINGLE structure exists for a protein - NOESY data for a range of lengths
- methyl groups often dealt with as a single atom - pseudo atoms