STRUCTURE OF DEOXYHEMOGLOBIN OF THE ANTARCTIC FISH PAGOTHENIA-BERNACCHII WITH AN ANALYSIS OF THE STRUCTURAL BASIS OF THE ROOT EFFECT BY COMPARISON OF THE LIGANDED AND UNLIGANDED HEMOGLOBIN STRUCTURES

被引:91
作者
ITO, N [1 ]
KOMIYAMA, NH [1 ]
FERMI, G [1 ]
机构
[1] MRC,MOLEC BIOL LAB,CAMBRIDGE CB2 2QH,ENGLAND
关键词
HEMOGLOBIN; ROOT EFFECT; TWINNING; CRYSTAL STRUCTURE; FISH;
D O I
10.1006/jmbi.1995.0405
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
We have determined the structure of deoxyhaemoglobin from the antarctic fish Pagothenia bernacchii at pH 6.2 to a resolution of 2.2 Angstrom with X-ray data from a twinned crystal deconvoluted so as to approximate data from a single crystal. The R-factor between the (twinned) model and the observed data is 16% for reflections used in refinement and 22% for reflections not used in refinement. The T (deoxy) structure was compared with the R (liganded) structure at pH 8.0 in an attempt to understand the structural basis of the greater affinity for hydrogen ions of T,relative to R, that comprises the Root effect. Up to half of the effect can be attributed to interaction of the residues Asp95 (G1)alpha and Asp101 (G3)beta: in R the residues are far apart and their carboxyl groups are unprotonated, but the shift at the alpha(1) beta(2) interface that accompanies the R to T transition brings them so close that they appear to share a proton between them. The proximity of Asp99 (G1)beta may contribute to the required raising of the pK(a) values of the other two Asp residues. These and neighbouring residues are sufficiently conserved in the haemoglobins of trout (component IV), carp and bluefin tuna, all of which exhibit the Root effect, for the same mechanism to apply. However, the environment is equally conserved in haemoglobins of Trematomus newnesi (major component) and trout (component I), which do not exhibit the Root effect, so that the structural factors controlling the Asp-Asp interaction remain unclear. No other residue appears to undergo an R to T change in the immediate neighbourhoods that could account for any significant portion of the Root effect, so at least half of the effect must result either from long-range electrostatic interactions or from a large number of local interactions. (C) 1995 Academic Press Limited
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页码:648 / 658
页数:11
相关论文
共 23 条
[1]  
[Anonymous], 1994, ACTA CRYSTALLOGR D, V50, P760
[2]   HEMOGLOBIN - STRUCTURAL-CHANGES RELATED TO LIGAND-BINDING AND ITS ALLOSTERIC MECHANISM [J].
BALDWIN, J ;
CHOTHIA, C .
JOURNAL OF MOLECULAR BIOLOGY, 1979, 129 (02) :175-+
[3]  
Baldwin J.M., 1975, Progress Biophys Molec Biol, V29, P225
[4]   CHLORIDE MASKS EFFECTS OF OPPOSING POSITIVE CHARGES IN HB-A AND HB HINSDALE (BETA-139 ASN-]LYS) THAT CAN MODULATE COOPERATIVITY AS WELL AS OXYGEN-AFFINITY [J].
BONAVENTURA, C ;
ARUMUGAM, M ;
CASHON, R ;
BONAVENTURA, J ;
MOOPENN, WF .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 239 (04) :561-568
[5]   FREE R-VALUE - A NOVEL STATISTICAL QUANTITY FOR ASSESSING THE ACCURACY OF CRYSTAL-STRUCTURES [J].
BRUNGER, AT .
NATURE, 1992, 355 (6359) :472-475
[6]   CRYSTALLOGRAPHIC REFINEMENT BY SIMULATED ANNEALING APPLICATION TO A 2.8-A RESOLUTION STRUCTURE OF ASPARTATE-AMINOTRANSFERASE [J].
BRUNGER, AT .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 203 (03) :803-816
[7]   HEMOGLOBIN OF THE ANTARCTIC FISH PAGOTHENIA-BERNACCHII - AMINO-ACID-SEQUENCE, OXYGEN EQUILIBRIA AND CRYSTAL-STRUCTURE OF ITS CARBONMONOXY DERIVATIVE [J].
CAMARDELLA, L ;
CARUSO, C ;
DAVINO, R ;
DIPRISCO, G ;
RUTIGLIANO, B ;
TAMBURRINI, M ;
FERMI, G ;
PERUTZ, MF .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 224 (02) :449-460
[8]  
DAVINO R, 1994, J BIOL CHEM, V269, P9675
[9]   STEREOCHEMISTRY OF CARBON-MONOXIDE BINDING TO NORMAL HUMAN ADULT AND COWTOWN HEMOGLOBINS [J].
DEREWENDA, Z ;
DODSON, G ;
EMSLEY, P ;
HARRIS, D ;
NAGAI, K ;
PERUTZ, M ;
REYNAUD, JP .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 211 (03) :515-519
[10]   3-DIMENSIONAL FOURIER SYNTHESIS OF HUMAN DEOXYHEMOGLOBIN AT 2.5-A RESOLUTION - REFINEMENT OF ATOMIC MODEL [J].
FERMI, G .
JOURNAL OF MOLECULAR BIOLOGY, 1975, 97 (02) :237-256