Isoelectric Point Determination for Glossoscolex paulistus Extracellular Hemoglobin: Oligomeric Stability in Acidic pH and Relevance to Protein-Surfactant Interactions


Autoria(s): SANTIAGO, Patricia S.; CARVALHO, Francisco Adriano O.; DOMINGUES, Marco M.; CARVALHO, Jose Wilson P.; SANTOS, Nuno C.; TABAK, Marcel
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

The extracellular hemoglobin from Glossoscolex paulistus (HbGp) has a molecular mass of 3.6 M Da, It has a high oligomeric stability at pH 7.0 and low autoxidation rates, as compared to vertebrate hemoglobins. In this work, fluorescence and light scattering experiments were performed with the three oxidation forms of HbGp exposed to acidic pH. Our focus is on the HbGp stability at acidic pH and also on the determination of the isoelectric point (pI) of the protein. Our results show that the protein in the cyanomet form is more stable than in the other two forms, in the whole range. Our zeta-potential data are consistent with light scattering results. Average values apt obtained by different techniques were 5.6 +/- 0.5, 5.4 +/- 0.2 and 5.2 +/- 0.5 for the oxy, met, and cyanomet forms. Dynamic light scattering (DLS) experiments have shown that, at pH 6.0, the aggregation (oligomeric) state of oxy-, met- and cyanomet-HbGp remains the same as that at 7.0. The interaction between the oxy-HbGp and ionic surfactants at pH 5.0 and 6.0 was also monitored in the present study. At pH 5,0, below the protein pI, the effects of sodium dodecyl sulfate (SDS) and cetyltrimethylammonium chloride (CTAC) are inverted when compared to pH 7.0. For CTAC, in acid pH 5.0, no precipitation is observed, while for SDS an intense light scattering appears due to a precipitation process. HbGp interacts strongly with the cationic surfactant at pH 7.0 and with the anionic one at pH 5.0. This effect is due to the predominance, in the protein surface, of residues presenting opposite charges to the surfactant headgroups. This information can be relevant for the development of extracellular hemoglobin-based artificial blood substitutes.

FAPESP

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq

CAPES

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

FCT-MCTES

Fundação para a Ciência e a Tecnologia de Portugal (FCT)

FCT-MCTES[SFRH/BD/41750/2007]

Fundação para a Ciência e a Tecnologia de Portugal (FCT)

Identificador

LANGMUIR, v.26, n.12, p.9794-9801, 2010

0743-7463

http://producao.usp.br/handle/BDPI/31877

10.1021/la100060p

http://dx.doi.org/10.1021/la100060p

Idioma(s)

eng

Publicador

AMER CHEMICAL SOC

Relação

Langmuir

Direitos

restrictedAccess

Copyright AMER CHEMICAL SOC

Palavras-Chave #DYNAMIC LIGHT-SCATTERING #BOVINE SERUM-ALBUMIN #LUMBRICUS-TERRESTRIS #VISCOSITY MEASUREMENTS #MET FORM #AUTOXIDATION #CHAIN #FLUORESCENCE #SPECTROSCOPY #PARTICLES #Chemistry, Multidisciplinary #Chemistry, Physical #Materials Science, Multidisciplinary
Tipo

article

original article

publishedVersion