Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Tipo de estudo
Intervalo de ano de publicação
1.
Biochim Biophys Acta ; 1752(2): 154-65, 2005 Sep 25.
Artigo em Inglês | MEDLINE | ID: mdl-16143573

RESUMO

beta-Lactoglobulin (beta-LG) denatured with 6 M guanidine hydrochloride (GdnHCl) containing a reducing agent and subsequently dialysed against phosphate-buffered saline (PBS) resulted in incomplete refolding of this protein despite the fact that the biological activity for retinol-binding was recovered to almost the same degree as that of the native molecule [Hattori, M., Ametani, A., Katakura, Y., Shimizu, M., Kaminogawa, S. J., Biol. Chem. 268 (1993) 22414-22419]. The enzyme probe method, evaluation of hydrophilicity values, in-gel mobility on SDS-PAGE, and evaluation of disulfide bonds with the Ellman method showed exposure of the hydrophobic region(s) and incorrect disulfide bond formation in such dialyzed beta-LG molecules. We reveal in this present work that complete refolding could be attained by diluting denatured beta-LG with PBS containing a reducing agent, before slow reoxidation of the sulfhydryl groups upon dialysis for gradient removal of the reducing agent in 6 steps. Complete renaturation was confirmed by analyzing the retinol-binding activity, CD spectra, intrinsic fluorescence, binding ability of monoclonal antibodies (mAbs), and SDS-PAGE. Step-by-step disulfide bond formation was considered to be critical for the complete refolding of denatured beta-LG. Our method can contribute to establish a procedure for complete refolding of useful recombinant proteins in vitro without such biological aids as chaperones.


Assuntos
Bovinos/metabolismo , Dissulfetos/metabolismo , Lactoglobulinas/metabolismo , Modelos Moleculares , Dobramento de Proteína , Animais , Anticorpos Monoclonais , Ácido Ditionitrobenzoico , Eletroforese em Gel de Poliacrilamida , Ensaio de Imunoadsorção Enzimática , Guanidina , Lactoglobulinas/fisiologia , Ligação Proteica , Desnaturação Proteica/fisiologia , Espectrometria de Fluorescência
2.
Biometrics ; 59(3): 512-20, 2003 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-14601752

RESUMO

In conventional line transect theory, it is assumed that all animals on the line are detected. This article introduces an extended and generalized hazard probability model without the need for such an assumption. The proposed method needs a survey design with independent observers having the same visual region and assumes an explicit distinction of simultaneous and delayed duplicates. It can take account of random heterogeneity caused by surfacing behavior as well as systematic heterogeneity by covariate effects. Furthermore, it can be easily extended to cases in which data from incompletely independent observers are available. The abundance estimate is based on the Horvitz-Thompson estimator in unequal detectability sampling scheme. Simulation studies suggest that the proposed method has good performance. The method is applied to a real data set on Antarctic minke whales in the illustration.


Assuntos
Mergulho , Densidade Demográfica , Animais , Regiões Antárticas , Biometria , Funções Verossimilhança , Modelos Estatísticos , Baleias
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...