Partial molar volumes of proteins:: amino acid side-chain contributions derived from the partial molar volumes of some tripeptides over the temperature range 10-90°C

被引:94
作者
Häckel, M
Hinz, HJ
Hedwig, GR
机构
[1] Massey Univ, Inst Fundamental Sci Chem, Palmerston North, New Zealand
[2] Univ Munster, Inst Physikal Chem, D-48149 Munster, Germany
关键词
partial molar volume; amino acid side-chains; group additivity; protein partial specific volumes; aqueous solution; tripeptides;
D O I
10.1016/S0301-4622(99)00104-0
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
The partial molar volumes of tripeptides of sequence glycyl-X-glycine, where X is one of the amino acids alanine, leucine, threonine, glutamine, phenylalanine, histidine, cysteine, proline, glutamic acid, and arginine, have been determined in aqueous solution over the temperature range 10-90 degrees C using differential scanning densimetry. These data, together with those reported previously, have been used to derive the partial molar volumes of the side-chains of all 20 amino acids. The side-chain volumes are critically compared with literature values derived using partial molar volumes for alternative model compounds. The new amino acid side-chain volumes, along with that for the backbone glycyl group, were used to calculate the partial specific volumes of several proteins in aqueous solution. The results obtained are compared with those observed experimentally. The new side-chain volumes have also been used to redetermine residue volume changes upon protein folding. (C) 1999 Elsevier Science B.V. All rights reserved.
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页码:35 / 50
页数:16
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