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Exploring Enzymatic Conformational Dynamics at Surfaces through µ-FTIR Spectromicroscopy.
Mendes, Giovana Rossi; Modenez, Iago de Assis; Cagnani, Giovana Rosso; Colombo, Rafael N P; Crespilho, Frank Nelson.
Afiliación
  • Mendes GR; São Carlos Institute of Chemistry, University of São Paulo, São Carlos 13560-970, Brazil.
  • Modenez IA; São Carlos Institute of Chemistry, University of São Paulo, São Carlos 13560-970, Brazil.
  • Cagnani GR; São Carlos Institute of Chemistry, University of São Paulo, São Carlos 13560-970, Brazil.
  • Colombo RNP; São Carlos Institute of Chemistry, University of São Paulo, São Carlos 13560-970, Brazil.
  • Crespilho FN; São Carlos Institute of Chemistry, University of São Paulo, São Carlos 13560-970, Brazil.
Anal Chem ; 95(30): 11254-11262, 2023 08 01.
Article en En | MEDLINE | ID: mdl-37459476
Immobilization of proteins onto solid supports has critical industrial, technological, and medical applications, and is a daily task in chemical research. Significant conformational rearrangements often occur due to enzyme-surface interactions, and it is of broad interest to develop methods to probe and better understand these molecular-level changes that contribute to the enzyme's catalytic activity and stability. While circular dichroism is a common method for solution-phase conformational study, the application to surface-supported proteins is not trivial and spatial mapping is not viable. On the other hand, a nonlinear laser spectroscopy technique used to analyze surfaces and interfaces is not often found in most laboratories, therefore requiring an alternative and reliable method. Here, we employed high-dimensional data spectromicroscopy analysis in the infrared region (µ-FTIR) to investigate the enzyme's conformational change when adsorbed onto solid matrices, across a ca. 20 mm2 area. Alcohol dehydrogenase (ADH) enzyme was adopted as a model enzyme to interact with CaF2, Au, and Au-thiol model substrates, strategically chosen for mapping the enzyme dynamics on solid surfaces with different polarity/hydrophobicity properties and extendable to other materials. Two-dimensional chemical maps indicate that the enzyme adsorbs with different patterns in which secondary structures dynamically adjust to optimize interprotein and enzyme-surface interactions. The results suggest an experimental approach to identify and map enzyme conformational dynamics onto different solid surfaces across space and provide insights into immobilized protein structure investigations for areas such as biosensing and bioenergy.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Idioma: En Revista: Anal Chem Año: 2023 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Idioma: En Revista: Anal Chem Año: 2023 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Estados Unidos