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Novel techniques for weak alignment of proteins in solution using chemical tags coordinating lanthanide ions
被引:113
作者:
Ikegami, T
Verdier, L
Sakhaii, P
Grimme, S
Pescatore, B
Saxena, K
Fiebig, KM
Griesinger, C
机构:
[1] Goethe Univ Frankfurt, Max Planck Inst Biophys Chem, Dept NMR Based Struct Biol, D-37077 Gottingen, Germany
[2] Inst Organ Chem, D-60439 Frankfurt, Germany
[3] Affinium Phamraceut, Toronto, ON M5J 1V6, Canada
基金:
日本学术振兴会;
关键词:
dipolar coupling;
disulfide bond;
lanthanide ion;
molecular alignment;
NMR;
D O I:
10.1023/B:JNMR.0000032611.72827.de
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
A molecule with an anisotropic magnetic susceptibility is spontaneously aligned in a static magnetic field. Alignment of such a molecule yields residual dipolar couplings and pseudocontact shifts. Lanthanide ions have recently been successfully used to provide an anisotropic magnetic susceptibility in target molecules either by replacing a calcium ion with a lanthanide ion in calcium-binding proteins or by attaching an EDTA derivative to a cysteine residue via a disulfide bond. Here we describe a novel enantiomerically pure EDTA derived tag that aligns stronger due to its shorter linker and does not suffer from stereochemical diversity upon lanthanide complexation. We observed residual N-15, H-1-dipolar couplings of up to 8 Hz at 800 MHz induced by a single alignment tensor from this tag.
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页码:339 / 349
页数:11
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