Neutron Laue diffractometry with an imaging plate provides an effective data collection for neutron protein crystallography

被引:2
作者
Niimura, N [1 ]
Minezaki, Y
Nonaka, T
Castagna, JC
Cipriani, F
Hoghoj, P
Lehmann, MS
Wilkinson, C
机构
[1] Japan Atom Energy Res Inst, Adv Sci Res Ctr, Tokai, Ibaraki 31911, Japan
[2] Nagaoka Univ Technol, Dept BioEngn, Nagaoka, Niigata, Japan
[3] EMBL Outstn, F-38042 Grenoble, France
[4] ILL, F-38042 Grenoble, France
来源
PHYSICA B | 1997年 / 241卷
关键词
neutron protein crystallography; hen Egg-White lysozyme; Laue diffractometry; neutron imaging plate;
D O I
10.1016/S0921-4526(97)00816-8
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Neutron Laue diffraction 2 Angstrom data from tetragonal hen egg-white (HEW) lysozyme were collected for 10 days with neutron imaging plates. All the 960 hydrogen atoms in the lysozyme and 157 bound water molecules could be identified. The final R-factor is 19.5%. Several interesting features of hydrogen atoms and bound water molecules of HEW-lysozyme were found as follows. (1) The crystal was grown at pH 7.0. There are no hydrogen (deuterium) atoms bound to carboxylate oxygen atoms of Glu35 and Asp52, which explains why lysozyme is less active at pH 7.0. (2) Hydrogen atoms and deuterium atoms are clearly identified. As an example, the omit map around indol ring of Trp 111 is shown. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1162 / 1165
页数:4
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