Phase memory relaxation times of spin labels in human carbonic anhydrase II:: pulsed EPR to determine spin label location

被引:40
作者
Huber, M
Lindgren, M
Hammarström, P
Mårtensson, LG
Carlsson, U
Eaton, GR
Eaton, SS
机构
[1] Leiden Univ, Dept Mol Phys, NL-2300 RA Leiden, Netherlands
[2] Linkoping Univ, IFM, Dept Chem Phys, S-58183 Linkoping, Sweden
[3] Linkoping Univ, IFM, Dept Biochem, S-58183 Linkoping, Sweden
[4] Univ Denver, Dept Chem & Biochem, Denver, CO 80208 USA
关键词
spin label EPR; relaxation; human carbonic anhydrase II; T-2;
D O I
10.1016/S0301-4622(01)00239-3
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
Phase memory relaxation times (T-M or T-2) of spin labels in human carbonic anhydrase II (HCA II) are reported. Spin labels (N-(1-oxyl-2,2,5,5-tetramethyl-3-pyrrolidinyl)iodoacetamide, IPSL) were introduced at cysteines, by site-directed mutagenesis at seven different positions in the protein. By two pulse electron paramagnetic resonance (EPR), electron spin echo decays at 45 K are measured and fitted by stretched exponentials, resulting in relaxation parameters T-M and x. T-M values of seven positions are between 1.6 mus for the most buried residue (L79C) and 4.7 mus for a residue at the protein surface (W245C). In deuteriated buffer, longer T-M are found for all but the most buried residues (L79C and W97C), and electron spin echo envelop modulation (ESEEM) of deuterium nuclei is observed. Different deuterium ESEEM patterns for W95C and W16C (surface residue) indicate differences in the local water concentration, or accessibility, of the spin label by deuterium. We propose T-M as a parameter to determine the spin label location in proteins. Furthermore, these systems are interesting for studying the pertaining relaxation mechanism. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:245 / 256
页数:12
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