Morphology and the strength of intermolecular contacts in protein crystals.
Morphology and the strength of intermolecular contacts in protein crystals.
复制标题
蛋白质晶体的形态和分子间接触的强度。
DOI:
10.1107/s0907444903011107
复制
发表时间:
2003
期刊:
影响因子:
--
通讯作者:
A. Chernov
中科院分区:
文献类型:
--
作者:
Y. Matsuura;A. Chernov
The strengths of intermolecular contacts (macrobonds) and the areas occupied by each contact on the molecular surface were estimated in four polymorphic modifications of lysozyme crystals based on the bond strengths between individual atomic pairs belonging to the molecules in contact. It has been shown that the periodic bond chains of these macrobonds account for the morphology of protein crystals. The Coulombic contribution to the macrobond strength has also been estimated. Making use of the contact strengths and taking into account bond hydration, crystal-water interfacial energies were also estimated for different crystal faces. The areas of all contacts are mapped on the molecular surface, making use of a polar-coordinate representation of the contact. Comparing the locations of the intermolecular contacts in the different polymorphic crystal modifications, it is shown that these contacts can form a wide variety of patches on the molecular surface. The patches are located practically everywhere on the surface except for the inside of a concave active site. It is also shown that the contacts, which frequently involve water molecules, are formed by specific intermolecular hydrogen bonds on a background of non-specific attractive electrostatic interactions. Typical values of the macrobond strength are compared with the strength of association in other protein-complex systems.
影响因子:
2.9
作者:
WOLFENDEN, R;ANDERSSON, L;SOUTHGATE, CCB
通讯作者:
SOUTHGATE, CCB
影响因子:
5.6
作者:
IPPOLITO, JA;ALEXANDER, RS;CHRISTIANSON, DW
通讯作者:
CHRISTIANSON, DW