Genetically encoded betaxanthin-based small-molecular fluorescent reporter for mammalian cells

Author:

Stücheli Pascal1,Sieber Simon2,Fuchs David W1,Scheller Leo1,Strittmatter Tobias1ORCID,Saxena Pratik1,Gademann Karl2,Fussenegger Martin13ORCID

Affiliation:

1. Department of Biosystems Science and Engineering, ETH Zurich, Mattenstrasse 26, CH-4058 Basel, Switzerland

2. Department of Chemistry, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland

3. Faculty of Science, University of Basel, Mattenstrasse 26, CH-4058 Basel, Switzerland

Abstract

Abstract We designed and engineered a dye production cassette encoding a heterologous pathway, including human tyrosine hydroxylase and Amanita muscaria 4,5-DOPA dioxygenase, for the biosynthesis of the betaxanthin family of plant and fungal pigments in mammalian cells. The system does not impair cell viability, and can be used as a non-protein reporter system to directly visualize the dynamics of gene expression by profiling absorbance or fluorescence in the supernatant of cell cultures, as well as for fluorescence labeling of individual cells. Pigment profiling can also be multiplexed with reporter proteins such as mCherry or the human model glycoprotein SEAP (secreted alkaline phosphatase). Furthermore, absorbance measurement with a smartphone camera using standard application software enables inexpensive, low-tech reporter quantification.

Funder

National Centre of Competence in Research

ETH Zurich NCCR Molecular Systems Engineering

Publisher

Oxford University Press (OUP)

Subject

Genetics

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