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Real-time monitoring of cell surface protein arrival with split luciferases.
Fischer, Alexandra A M; Schatz, Larissa; Baaske, Julia; Römer, Winfried; Weber, Wilfried; Thuenauer, Roland.
Afiliación
  • Fischer AAM; Signaling Research Centres BIOSS and CIBSS and Faculty of Biology, University of Freiburg, Freiburg, Germany.
  • Schatz L; Faculty of Biology, University of Freiburg, Freiburg, Germany.
  • Baaske J; Spemann Graduate School of Biology and Medicine (SGBM), University of Freiburg, Freiburg, Germany.
  • Römer W; Centre for Structural Systems Biology (CSSB), Hamburg, Germany.
  • Weber W; Technology Platform Light Microscopy, University of Hamburg, Hamburg, Germany.
  • Thuenauer R; Signaling Research Centres BIOSS and CIBSS and Faculty of Biology, University of Freiburg, Freiburg, Germany.
Traffic ; 24(10): 453-462, 2023 10.
Article en En | MEDLINE | ID: mdl-37403269
Each cell in a multicellular organism permanently adjusts the concentration of its cell surface proteins. In particular, epithelial cells tightly control the number of carriers, transporters and cell adhesion proteins at their plasma membrane. However, sensitively measuring the cell surface concentration of a particular protein of interest in live cells and in real time represents a considerable challenge. Here, we introduce a novel approach based on split luciferases, which uses one luciferase fragment as a tag on the protein of interest and the second fragment as a supplement to the extracellular medium. Once the protein of interest arrives at the cell surface, the luciferase fragments complement and generate luminescence. We compared the performance of split Gaussia luciferase and split Nanoluciferase by using a system to synchronize biosynthetic trafficking with conditional aggregation domains. The best results were achieved with split Nanoluciferase, for which luminescence increased more than 6000-fold upon recombination. Furthermore, we showed that our approach can separately detect and quantify the arrival of membrane proteins at the apical and basolateral plasma membrane in single polarized epithelial cells by detecting the luminescence signals with a microscope, thus opening novel avenues for characterizing the variations in trafficking in individual epithelial cells.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Epiteliales / Proteínas de la Membrana Idioma: En Revista: Traffic Asunto de la revista: FISIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Epiteliales / Proteínas de la Membrana Idioma: En Revista: Traffic Asunto de la revista: FISIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido