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• W2913454360 abstract "Complementation-dependent fluorescence is a powerful way to study co-localization or interactions between biomolecules. A split-GFP variant, involving the self-associating GFP 1-10 and GFP 11, has previously provided a convenient approach to measure recombinant protein titers in cell supernatants. A limitation of this approach is the slow chromophore formation after complementation. Here, we alleviate this lag in signal generation by allowing the GFP 1-10 chromophore to mature on a solid support containing GFP 11 before applying GFP 1-10 in analyses. The pre-maturated GFP 1-10 provided up to 150-fold faster signal generation compared to the non-maturated version. Moreover, pre-maturated GFP 1-10 significantly improved the ability of discriminating between Chinese hamster ovary (CHO) cell lines secreting GFP 11-tagged erythropoietin protein at varying rates. Its improved kinetics make the pre-maturated GFP 1-10 a suitable reporter molecule for cell biology research in general, especially for ranking individual cell lines based on secretion rates of recombinant proteins." @default.
• W2913454360 created "2019-02-21" @default.
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• W2913454360 date "2019-01-22" @default.
• W2913454360 modified "2023-10-06" @default.
• W2913454360 title "Chromophore pre-maturation for improved speed and sensitivity of split-GFP monitoring of protein secretion" @default.
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• W2913454360 doi "https://doi.org/10.1038/s41598-018-36559-x" @default.
• W2913454360 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6342966" @default.
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