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Determination of Heteronuclear Three-bond J-coupling Constants in Peptides by a Simple Heteronuclear Relayed E.COSY Experiment

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Journal J Biomol NMR
Publisher Springer
Date 1995 Jul 1
PMID 7663145
Citations 4
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Abstract

A simple heteronuclear relayed E.COSY pulse sequence with a minimum number of pulses is proposed for the quantitative determination of heteronuclear three-bond J-coupling constants in uniformly 13C-enriched polypeptide samples. Numerous heteronuclear three-bond coupling constants, including 3JHNC, 3JHNC beta, 3JH beta C, and 3JH alpha C gamma, can be determined for each residue from a single heteronuclear relayed E.COSY spectrum. Couplings relevant for stereospecific assignments as well as for the determination of dihedral angles in the amino acid backbone and in side chains are obtained. The method is demonstrated on the uniformly 13C-enriched decapeptide antamanide (-Val1-Pro2-Pro3-Ala4-Phe5-Phe6-Pro7-Pro8-Phe9-Phe1 0-).

Citing Articles

Self-consistent 3J coupling analysis for the joint calibration of Karplus coefficients and evaluation of torsion angles.

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Alternative E.COSY techniques for the measurement of 3J(C (i) (') (-1),C (i) (beta) ) and (3) J(H (i) (N) ,C (i) (beta) ) coupling constants in proteins.

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Heteronuclear relayed E.COSY revisited: determination of 3J(H(alpha),C(gamma)) couplings in Asx and aromatic residues in proteins.

Lohr F, Perez C, Kohler R, Ruterjans H, Schmidt J J Biomol NMR. 2000; 18(1):13-22.

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Heteronuclear relayed E.COSY applied to the determination of accurate 3J(HN,C') and 3J(H beta,C') coupling constants in desulfovibrio vulgaris flavodoxin.

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References
1.
Ponder J, Richards F . Tertiary templates for proteins. Use of packing criteria in the enumeration of allowed sequences for different structural classes. J Mol Biol. 1987; 193(4):775-91. DOI: 10.1016/0022-2836(87)90358-5. View

2.
Janin J, Wodak S . Conformation of amino acid side-chains in proteins. J Mol Biol. 1978; 125(3):357-86. DOI: 10.1016/0022-2836(78)90408-4. View

3.
Schmidt J, Ruterjans H, Schwalbe H, Greisinger C . Conformation of valine side chains in ribonuclease T1 determined by NMR studies of homonuclear and heteronuclear 3J coupling constants. Biochemistry. 1994; 33(18):5481-92. DOI: 10.1021/bi00184a017. View

4.
Delaglio F, Torchia D, Bax A . Measurement of 15N-13C J couplings in staphylococcal nuclease. J Biomol NMR. 1991; 1(4):439-46. DOI: 10.1007/BF02192865. View

5.
Schmieder P, Kurz M, Kessler H . Determination of heteronuclear long-range couplings to heteronuclei in natural abundance by two- and three-dimensional NMR spectroscopy. J Biomol NMR. 1991; 1(4):403-20. DOI: 10.1007/BF02192863. View