A fast and accurate procedure to collect and analyze unfolding fluorescence signal: the case of dystroglycan domains.
Biophys Chem
; 107(2): 197-211, 2004 Feb 01.
Article
em En
| MEDLINE
| ID: mdl-14962600
ABSTRACT
Monitoring the fluorescence signal upon unfolding often represents a very effective method to rapidly retrieve the first preliminary structural information on a protein domain. The relationship between intrinsic fluorescence signals and unfolding of proteins are discussed, including several practical considerations for properly setting fluorescence experiments and the phenomenological equations required to analyze the spectra. In particular, a fast and accurate method which allows to minimize the deleterious effect of photobleaching is provided. A number of unfolding reactions relative to immunoglobulins (IgG and IgM) and to the different domains of the adhesion molecule dystroglycan are presented. Special attention is dedicated to a alpha-dystroglycan immunoglobulin-like domain showing a "reverse" behavior of the fluorescence signal as a function of the denaturing agent concentration.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Glicoproteínas de Membrana
/
Dobramento de Proteína
/
Proteínas do Citoesqueleto
Tipo de estudo:
Qualitative_research
Idioma:
En
Ano de publicação:
2004
Tipo de documento:
Article