Title: NMR of protein
1NMR of protein
21H NMR spectra of small protein
3Protein folded and unfolded
Folded
Unfolded
42D-COSY
52D-COSY NH/CHa expanded region
62D-NOESY
7sequential assignment using NOESY
- In the a-helix the neighbouring HN are 2.8
Ångström apart - In the ß-strand the distance from Ha in residue
(i) to HN in residue (i1) is only 2.2 Ångström.
8Schematic presentation NOESY spectrum in the NH
region
The diagonal cross peaks are marked as black
signals labeled 1 to 9. The red cross peaks are
sequential NOEs.
If 2Val (V), 5 from a tryptophan (W) and 9 from
a glycine (G), we can write that sequence
is XVXXXWXXG or GXXWXXXVX 983567421 sequence of
signals GAKWSRYVP amino acid sequence
1 ? 2 ? 4 ? 7 ? 6 ? 5 ? 3 ? 8 ? 9
Or reverse
9Sequential Assignment of Ha in residue (i) to NH
in residue (i1) by NOE
Superimposition of a COSY spectrum with blue
annotated cross peaks (through bond) and NOESY
spectrum with red cross peaks. Sequential NOE
between Ha in residue (i) to HN in residue (i1).
CH1/NH5
6 ? 4 ? 1? 5 ? 7 ? 3 ? 2
CH4/NH1
CH6
NH6
NH4
10NOE-distance
using distance constraints to calculate a
structure. In the upper figure is shown a linear
strand with beads. The green, red and blue pairs
of beads, respectively have been shown to be
close to each other. The structure below
represents one solution to determining the
structure based on the three pieces of distance
information.
11Coupling values to setup experiments
140 Hz
H
15 Hz
11 Hz
55 Hz
13C
13C
15N
13C
15N
O
O
H
H
13C
90-100 Hz
30-40 Hz
123D-HMQC-COSY
13HMQC-NOESY
NH 1
2
Ha1
Ca1
2
3
Ha2
Ca2
3
4
Ca3
14HMQC-NOESY
R. R. Ernst (nobel lecture 92)
153D-HMQC-NOESY
162D-NOESY vs 3D-HMQC-NOESY
17NOESY-HMQC
Ha-1
Ha1
NH1
Ha2
NH2
Ha1
Ha3
Ha2
NH3
L.E.Kay, D.Marion, A.Bax, J.Magn.Reson.,84, 72
(89)
182D and 3D HMQC-TOCSY
193D HCCH-TOCSY
203D-NMR Puzzle approach
HNCA
HN(CO)CA
HNCO
213D-NMR Puzzle approach
HA(CA)NH
HACACO
HCA(CO)N
22HNCACB CBCA(CO)NH
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24Figure 19. Schematic presentation of the combined
spectrum analysis of the three-dimensional HNCACB
and a CBCA(CO)NH spectra. The 15N axis and the
frames in the 15N dimension are coloured blue.
The1H axis and the frames in the 1H dimension are
coloured red. The 13C axis and the frames in the
13C dimension are green. Two planes dN(i),
top-left, and dN(i1), bottom-left, are
highlighted. The cross peaks in HNCACB are and
in CBCA(CO)NH are
25HNCO 2D and 3D
26HN(CA)CO and HNCOcomplementary experiments
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28Example of HNCA and HN(CO)CA
29Example of sequential assignment
302D HN(CO)(CA)
NH
314D-NMR