Your browser doesn't support javascript.
loading
Determination of Secondary Structure of Proteins by Nanoinfrared Spectroscopy.
Waeytens, Jehan; De Meutter, Joëlle; Goormaghtigh, Erik; Dazzi, Alexandre; Raussens, Vincent.
Afiliação
  • Waeytens J; Center for Structural Biology and Bioinformatics, Laboratory for the Structure and Function of Biological Membranes, Université libre de Bruxelles, 1050Brussels, Belgium.
  • De Meutter J; Institut de Chimie Physique d'Orsay, CNRS UMR8000, Université Paris-Saclay, 91400Orsay, France.
  • Goormaghtigh E; Center for Structural Biology and Bioinformatics, Laboratory for the Structure and Function of Biological Membranes, Université libre de Bruxelles, 1050Brussels, Belgium.
  • Dazzi A; Center for Structural Biology and Bioinformatics, Laboratory for the Structure and Function of Biological Membranes, Université libre de Bruxelles, 1050Brussels, Belgium.
  • Raussens V; Institut de Chimie Physique d'Orsay, CNRS UMR8000, Université Paris-Saclay, 91400Orsay, France.
Anal Chem ; 95(2): 621-627, 2023 01 17.
Article em En | MEDLINE | ID: mdl-36598929
ABSTRACT
Nanoscale infrared spectroscopy (AFMIR) is becoming an important tool for the analysis of biological sample, in particular protein assemblies, at the nanoscale level. While the amide I band is usually used to determine the secondary structure of proteins in Fourier transform infrared spectroscopy, no tool has been developed so far for AFMIR. The paper introduces a method for the study of secondary structure of protein based on a protein library of 38 well-characterized proteins. Ascending stepwise linear regression (ASLR) and partial least square (PLS) regression were used to correlate spectrum characteristic bands with the major secondary structures (α-helixes and ß-sheets). ASLR appears to provide better results than PLS. The secondary structure predictions are characterized by a root mean square standard error in a cross validation of 6.39% for α-helixes and 6.23% for ß-sheets.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas / Amidas Tipo de estudo: Prognostic_studies Idioma: En Revista: Anal Chem Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas / Amidas Tipo de estudo: Prognostic_studies Idioma: En Revista: Anal Chem Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Bélgica