dc.contributorInst Quim Sao Carlos
dc.contributorUniv Estado Mato Grosso
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-11-26T17:06:27Z
dc.date.available2018-11-26T17:06:27Z
dc.date.created2018-11-26T17:06:27Z
dc.date.issued2016-09-01
dc.identifierEuropean Biophysics Journal With Biophysics Letters. New York: Springer, v. 45, n. 6, p. 549-563, 2016.
dc.identifier0175-7571
dc.identifierhttp://hdl.handle.net/11449/161994
dc.identifier10.1007/s00249-016-1121-6
dc.identifierWOS:000384722500006
dc.identifierWOS000384722500006.pdf
dc.identifier6705367010662087
dc.identifier0000-0002-6205-9441
dc.description.abstractOxy-HbRa thermal stability was evaluated by dynamic light scattering (DLS) and small-angle X-ray scattering (SAXS) at pH 5.0, 7.0, 8.0, and 9.0. DLS results show that oxy-HbRa, at pH 7.0 and 5.0, remains stable up to 56 degrees C, undergoing denaturation/aggregation in acidic media above 60 degrees C, followed by partial sedimentation of aggregates. At alkaline pH values 8.0 and 9.0, oxy-HbRa oligomeric dissociation is observed above 30 degrees C, before denaturation. SAXS data show that oxy-HbRa, at 20 degrees C, is in its native form, displaying radius of gyration (R-g) and particle maximum dimension (D-max) of 108 +/- 1 and 300 +/- 10 angstrom, respectively. Oxy-HbRa, at pH 7.0, undergoes denaturation/aggregation at 60 degrees C. At pH 5.0-6.0, HbRa thermal denaturation/aggregation start earlier, at 50 degrees C, accompanied by an increase of R-g and D-max values. However, an overlap of oligomeric dissociation and denaturation in the system is observed upon temperature increase, with an increase in R-g and D-max. Analysis of experimental p(r) curves as a linear combination of theoretical curves obtained for HbGp fragments from the crystal structure shows an increasing contribution of dodecamer (abcd)(3) and tetramer (abcd) in solution, as a function of pH values (8.0 and 9.0) and temperature. Finally, our data show, for the first time, that oxy-HbRa, in neutral and acidic media, does not undergo oligomeric dissociation before denaturation, while in alkaline media the oligomeric dissociation process is an important step in the thermal denaturation.
dc.languageeng
dc.publisherSpringer
dc.relationEuropean Biophysics Journal With Biophysics Letters
dc.relation0,604
dc.rightsAcesso aberto
dc.sourceWeb of Science
dc.subjectErythrocruorins
dc.subjectThermal stability
dc.subjectDenaturation/aggregation
dc.subjectOligomeric dissociation
dc.subjectpH
dc.titleThermal stability of extracellular hemoglobin of Rhinodrilus alatus (HbRa): DLS and SAXS studies
dc.typeArtículos de revistas


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