4.6 Article

Development of a rapid polarized total synchronous fluorescence spectroscopy (pTSFS) method for protein quantification in a model bioreactor broth

Journal

BIOTECHNOLOGY AND BIOENGINEERING
Volume 118, Issue 5, Pages 1805-1817

Publisher

WILEY
DOI: 10.1002/bit.27694

Keywords

bioprocess monitoring; chemometrics; multidimensional fluorescence; polarization; process analytical technology; protein

Funding

  1. Science Foundation Ireland [14/IA/2282]
  2. European Regional Development Fund [14/IA/2282]
  3. Science Foundation Ireland (SFI) [14/IA/2282] Funding Source: Science Foundation Ireland (SFI)

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This study developed a new method for protein quantification in bioreactor broth using polarized total synchronous fluorescence spectroscopy, which showed better analytical performance compared to traditional methods. By optimizing the process, faster online measurements and more accurate results were achieved.
Protein quantification during bioprocess monitoring is essential for biopharmaceutical manufacturing and is complicated by the complex chemical composition of the bioreactor broth. Here we present the early-stage development and optimization of a polarized total synchronous fluorescence spectroscopy (pTSFS) method for protein quantification in a hydrolysate-protein model (mimics clarified bioreactor broth samples) using a standard benchtop laboratory fluorometer. We used UV transmitting polarizers to provide wider range pTSFS spectra for screening of the four different TSFS spectra generated by the measurement: parallel (||), perpendicular (perpendicular to), unpolarized (T) intensity spectra and anisotropy maps. TSFS|| (parallel polarized) measurements were the best for protein quantification compared to standard unpolarized measurements and the Bradford assay. This was because TSFS|| spectra had a better analyte signal to noise ratio (SNR), due to the anisotropy of protein emission. This meant that protein signals were better resolved from the background emission of small molecule fluorophores in the cell culture media. SNR of >5000 was achieved for concentrations of bovine serum albumin/yeastolate 1.2/10 g L-1 with TSFS||. Optimization using genetic algorithm and interval partial least squares based variable selection enabled reduction of spectral resolution and number of excitation wavelengths required without degrading performance. This enables fast (<3.5 min) online/at-line measurements, and the method had an LOD of 0.18 g L-1 and high accuracy with a predictive error of <9%.

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