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Optimization of proximity ligation assay (PLA) for detection of protein interactions and fusion proteins in non-adherent cells: application to pre-B lymphocytes.
Debaize, Lydie; Jakobczyk, Hélène; Rio, Anne-Gaëlle; Gandemer, Virginie; Troadec, Marie-Bérengère.
Afiliación
  • Debaize L; Institut de Génétique et Développement de Rennes, UMR 6290 CNRS, Université de Rennes 1, UBL, 2 avenue du Professeur Léon Bernard, 35043 RENNES CEDEX, France.
  • Jakobczyk H; SFR Biosit UMS CNRS 3480/US INSERM 018, Rennes, France.
  • Rio AG; Institut de Génétique et Développement de Rennes, UMR 6290 CNRS, Université de Rennes 1, UBL, 2 avenue du Professeur Léon Bernard, 35043 RENNES CEDEX, France.
  • Gandemer V; SFR Biosit UMS CNRS 3480/US INSERM 018, Rennes, France.
  • Troadec MB; Institut de Génétique et Développement de Rennes, UMR 6290 CNRS, Université de Rennes 1, UBL, 2 avenue du Professeur Léon Bernard, 35043 RENNES CEDEX, France.
Mol Cytogenet ; 10: 27, 2017.
Article en En | MEDLINE | ID: mdl-28736577
ABSTRACT

BACKGROUND:

Genetic abnormalities, including chromosomal translocations, are described for many hematological malignancies. From the clinical perspective, detection of chromosomal abnormalities is relevant not only for diagnostic and treatment purposes but also for prognostic risk assessment. From the translational research perspective, the identification of fusion proteins and protein interactions has allowed crucial breakthroughs in understanding the pathogenesis of malignancies and consequently major achievements in targeted therapy.

METHODS:

We describe the optimization of the Proximity Ligation Assay (PLA) to ascertain the presence of fusion proteins, and protein interactions in non-adherent pre-B cells. PLA is an innovative method of protein-protein colocalization detection by molecular biology that combines the advantages of microscopy with the advantages of molecular biology precision, enabling detection of protein proximity theoretically ranging from 0 to 40 nm.

RESULTS:

We propose an optimized PLA procedure. We overcome the issue of maintaining non-adherent hematological cells by traditional cytocentrifugation and optimized buffers, by changing incubation times, and modifying washing steps. Further, we provide convincing negative and positive controls, and demonstrate that optimized PLA procedure is sensitive to total protein level. The optimized PLA procedure allows the detection of fusion proteins and protein interactions on non-adherent cells.

CONCLUSION:

The optimized PLA procedure described here can be readily applied to various non-adherent hematological cells, from cell lines to patients' cells. The optimized PLA protocol enables detection of fusion proteins and their subcellular expression, and protein interactions in non-adherent cells. Therefore, the optimized PLA protocol provides a new tool that can be adopted in a wide range of applications in the biological field.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Guideline Idioma: En Revista: Mol Cytogenet Año: 2017 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Guideline Idioma: En Revista: Mol Cytogenet Año: 2017 Tipo del documento: Article País de afiliación: Francia