TY - JOUR
T1 - α&β HSQC, an HSQC-Type experiment with improved resolution for I2S groups
AU - Sattler, M.
AU - Schleucher, J.
AU - Schedletzky, O.
AU - Glaser, S. J.
AU - Griesinger, C.
AU - Nielsen, N. C.
AU - Sørensen, O. W.
N1 - Funding Information:
This work was supported by the ‘‘Fonds der Chemischen Industrie’’ and the DFG under Grant Gr1211/6-1 to C.G. We thank Hoechst AG, Frankfurt, Germany, for the gift of LHRH and Dr. U. Weydemann, Rhein Biotech, for the preparation of Rhodniin. Furthermore, scholarships of the Graduier-tenkolleg, ‘‘Chemische und Biologische Synthese von Wirkstoffen,’’ Eg 52/3-3 (J. Schleucher), and a Heisenberg-scholarship of the DFG, G1 203/ 2-1 (S. J. Glaser), are gratefully acknowledged. O.S. is supported by the DFG under Gr1211/6-1.
PY - 1996
Y1 - 1996
N2 - A new HSQC-type pulse scheme is introduced that effectively improves the spectral resolution by what corresponds to the size of geminal JHH coupling constants, i.e., on the order of -14 Hz in CH2 groups of peptides and proteins. The gain in resolution comes from the fact that, in I2S groups with I-spin detection, only those resonances with the passive I spin being in either the α or the β state are excited. The experiment α&β HSQC has two versions: one that is α and β selective in the echo and antiecho parts, respectively, or the opposite combination. This selection of polarizing only one half of the I-spin resonances works even when the two I spins are strongly coupled. Pure-absorption, selective α HSQC or β HSQC spectra are obtained by the two combinations of the echo part of one of the α&β HSQC spectra with the antiecho part of the other. These two spectra (α HSQC and β HSQC) can be merged into another spectrum, Mab HSQC, which has the appearance of an HSQC spectrum with homonuclear broadband decoupling of geminal scalar interactions. The method is demonstrated on aqueous solutions of a decapeptide at the natural-abundance level of isotopes and on the protein rhodniin (103 residues) uniformly labeled with 13C and 15N.
AB - A new HSQC-type pulse scheme is introduced that effectively improves the spectral resolution by what corresponds to the size of geminal JHH coupling constants, i.e., on the order of -14 Hz in CH2 groups of peptides and proteins. The gain in resolution comes from the fact that, in I2S groups with I-spin detection, only those resonances with the passive I spin being in either the α or the β state are excited. The experiment α&β HSQC has two versions: one that is α and β selective in the echo and antiecho parts, respectively, or the opposite combination. This selection of polarizing only one half of the I-spin resonances works even when the two I spins are strongly coupled. Pure-absorption, selective α HSQC or β HSQC spectra are obtained by the two combinations of the echo part of one of the α&β HSQC spectra with the antiecho part of the other. These two spectra (α HSQC and β HSQC) can be merged into another spectrum, Mab HSQC, which has the appearance of an HSQC spectrum with homonuclear broadband decoupling of geminal scalar interactions. The method is demonstrated on aqueous solutions of a decapeptide at the natural-abundance level of isotopes and on the protein rhodniin (103 residues) uniformly labeled with 13C and 15N.
UR - http://www.scopus.com/inward/record.url?scp=0000801097&partnerID=8YFLogxK
U2 - 10.1006/jmra.1996.0070
DO - 10.1006/jmra.1996.0070
M3 - Article
AN - SCOPUS:0000801097
SN - 1064-1858
VL - 119
SP - 171
EP - 179
JO - Journal of Magnetic Resonance, Series A
JF - Journal of Magnetic Resonance, Series A
IS - 2
ER -