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Small-angle X-ray scattering reveals differences between the quaternary structures of oxygenated and deoxygenated tarantula hemocyanin

Identifieur interne : 003E57 ( Main/Exploration ); précédent : 003E56; suivant : 003E58

Small-angle X-ray scattering reveals differences between the quaternary structures of oxygenated and deoxygenated tarantula hemocyanin

Auteurs : Heinz Decker [Allemagne] ; Hermann Hartmann [Allemagne] ; Reinhard Sterner [Suisse] ; Erika Schwarz [Autriche] ; Ingrid Pilz [Autriche]

Source :

RBID : ISTEX:E275947F23AA18C6165CD0911AD2C5330557BDA1

English descriptors

Abstract

Abstract: Small-angle X-ray scattering (SAXS) curves have been recorded for the oxygenated and deoxygenated states of the 4 × 6-meric hemocyanin from the tarantula Eurypelma californicum. A comparison of the curves shows that the quaternary structures of the two states are different by three criteria, which all indicate that the hemocyanin is less compact in the oxygenated compared to the deoxygenated form: (a) The radius of gyration is 8.65 ± 0.05 nm for the deoxy- and 8.80 ± 0.05 nm for the oxy-form. (b) The maximum particle dimension amounts to 25.0 ± 0.5 nm for the deoxy- and to 27.0 ± 0.5 nm for the oxyform. (c) A dip in the intramolecular distance distribution function p(r) is more pronounced and shifted to larger distances in the oxy-form. The p(r) functions based on SAXS measurements were compared to p(r) functions deduced from published electron microscopical images of three different 4 × 6-meric hemocyanins from closely related species. The p(r) functions of SAXS and electron microscopy were similar in one case, whereas in the other two cases the distance between the two 12-meric half-molecules had to be changed by 1–1.5 nm to obtain good agreement. The differences between the p(r) functions of oxygenated and deoxygenated 4 × 6-meric tarantula hemocyanin are much larger than one would expect from a comparison of X-ray structures of the oxygenated and deoxygenated states of a closely related 6-meric hemocyanin. Thus, the conformational changes upon oxygenation occur at various levels of the quaternary structure, as postulated by hierarchical theories of allosteric interactions.

Url:
DOI: 10.1016/0014-5793(96)00887-3


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Le document en format XML

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<term>Conformational changes</term>
<term>Decker</term>
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<term>Deoxygenated hemocyanin</term>
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<term>Hemocyanins</term>
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<term>Oxygen binding</term>
<term>Oxygenated</term>
<term>Physiol</term>
<term>Polyphemus</term>
<term>Quaternary</term>
<term>Quaternary structure</term>
<term>Saxs measurements</term>
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<div type="abstract" xml:lang="en">Abstract: Small-angle X-ray scattering (SAXS) curves have been recorded for the oxygenated and deoxygenated states of the 4 × 6-meric hemocyanin from the tarantula Eurypelma californicum. A comparison of the curves shows that the quaternary structures of the two states are different by three criteria, which all indicate that the hemocyanin is less compact in the oxygenated compared to the deoxygenated form: (a) The radius of gyration is 8.65 ± 0.05 nm for the deoxy- and 8.80 ± 0.05 nm for the oxy-form. (b) The maximum particle dimension amounts to 25.0 ± 0.5 nm for the deoxy- and to 27.0 ± 0.5 nm for the oxyform. (c) A dip in the intramolecular distance distribution function p(r) is more pronounced and shifted to larger distances in the oxy-form. The p(r) functions based on SAXS measurements were compared to p(r) functions deduced from published electron microscopical images of three different 4 × 6-meric hemocyanins from closely related species. The p(r) functions of SAXS and electron microscopy were similar in one case, whereas in the other two cases the distance between the two 12-meric half-molecules had to be changed by 1–1.5 nm to obtain good agreement. The differences between the p(r) functions of oxygenated and deoxygenated 4 × 6-meric tarantula hemocyanin are much larger than one would expect from a comparison of X-ray structures of the oxygenated and deoxygenated states of a closely related 6-meric hemocyanin. Thus, the conformational changes upon oxygenation occur at various levels of the quaternary structure, as postulated by hierarchical theories of allosteric interactions.</div>
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