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Incorporation of an Unnatural Amino Acid as a Domain-Specific Fluorescence Probe in a Two-Domain Protein.
Ries, Lena K; Schmid, Franz X; Schmidpeter, Philipp A M.
Afiliação
  • Ries LK; Laboratorium für Biochemie und Bayreuther Zentrum für Molekulare Biowissenschaften, Universität Bayreuth , Universitätsstraße 30, D-95447 Bayreuth, Germany.
  • Schmid FX; Laboratorium für Biochemie und Bayreuther Zentrum für Molekulare Biowissenschaften, Universität Bayreuth , Universitätsstraße 30, D-95447 Bayreuth, Germany.
  • Schmidpeter PA; Laboratorium für Biochemie und Bayreuther Zentrum für Molekulare Biowissenschaften, Universität Bayreuth , Universitätsstraße 30, D-95447 Bayreuth, Germany.
Biochemistry ; 55(49): 6739-6742, 2016 Dec 13.
Article em En | MEDLINE | ID: mdl-27951650
ABSTRACT
The biophysical analysis of multidomain proteins often is difficult because of overlapping signals from the individual domains. Previously, the fluorescent unnatural amino acid p-cyanophenylalanine has been used to study the folding of small single-domain proteins. Here we extend its use to a two-domain protein to selectively analyze the folding of a specific domain within a multidomain protein.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Corantes Fluorescentes / Aminoácidos Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Corantes Fluorescentes / Aminoácidos Idioma: En Ano de publicação: 2016 Tipo de documento: Article