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Characterization of homodimer interfaces with cross-linking mass spectrometry and isotopically labeled proteins.
Lima, Diogo B; Melchior, John T; Morris, Jamie; Barbosa, Valmir C; Chamot-Rooke, Julia; Fioramonte, Mariana; Souza, Tatiana A C B; Fischer, Juliana S G; Gozzo, Fabio C; Carvalho, Paulo C; Davidson, W Sean.
Afiliación
  • Lima DB; Mass Spectrometry for Biology Unit, CNRS USR 2000, Institut Pasteur, Paris, France.
  • Melchior JT; Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
  • Morris J; Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
  • Barbosa VC; Systems Engineering and Computer Science Program, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Chamot-Rooke J; Mass Spectrometry for Biology Unit, CNRS USR 2000, Institut Pasteur, Paris, France.
  • Fioramonte M; Dalton Mass Spectrometry Laboratory, University of Campinas, São Paulo, Brazil.
  • Souza TACB; Group for Computational Mass Spectrometry & Proteomics, Carlos Chagas Institute, Fiocruz Paraná, Brazil.
  • Fischer JSG; Group for Computational Mass Spectrometry & Proteomics, Carlos Chagas Institute, Fiocruz Paraná, Brazil.
  • Gozzo FC; Dalton Mass Spectrometry Laboratory, University of Campinas, São Paulo, Brazil.
  • Carvalho PC; Group for Computational Mass Spectrometry & Proteomics, Carlos Chagas Institute, Fiocruz Paraná, Brazil.
  • Davidson WS; Laboratory of Toxinology, Fiocruz, Rio de Janeiro, Brazil.
Nat Protoc ; 13(3): 431-458, 2018 03.
Article en En | MEDLINE | ID: mdl-29388937
Cross-linking coupled with mass spectrometry (XL-MS) has emerged as a powerful strategy for the identification of protein-protein interactions, characterization of interaction regions, and obtainment of structural information on proteins and protein complexes. In XL-MS, proteins or complexes are covalently stabilized with cross-linkers and digested, followed by identification of the cross-linked peptides by tandem mass spectrometry (MS/MS). This provides spatial constraints that enable modeling of protein (complex) structures and regions of interaction. However, most XL-MS approaches are not capable of differentiating intramolecular from intermolecular links in multimeric complexes, and therefore they cannot be used to study homodimer interfaces. We have recently developed an approach that overcomes this limitation by stable isotope-labeling of one of the two monomers, thereby creating a homodimer with one 'light' and one 'heavy' monomer. Here, we describe a step-by-step protocol for stable isotope-labeling, followed by controlled denaturation and refolding in the presence of the wild-type protein. The resulting light-heavy dimers are cross-linked, digested, and analyzed by mass spectrometry. We show how to quantitatively analyze the corresponding data with SIM-XL, an XL-MS software with a module tailored toward the MS/MS data from homodimers. In addition, we provide a video tutorial of the data analysis with this protocol. This protocol can be performed in ∼14 d, and requires basic biochemical and mass spectrometry skills.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Espectrometría de Masas en Tándem / Marcaje Isotópico Idioma: En Revista: Nat Protoc Año: 2018 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Espectrometría de Masas en Tándem / Marcaje Isotópico Idioma: En Revista: Nat Protoc Año: 2018 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido