Publications by authors named "Nuria De Mas"

Article Synopsis
  • A disulfide-bridged peptide drug candidate consists of two oligopeptide chains with 11 and 12 amino acids, linked by a disulfide bond at one end.
  • A biotechnology process was developed to efficiently produce these peptides by separately creating each oligopeptide chain in E. coli, then combining them through cleavage and chemical reactions.
  • A novel heterodimeric system using a leucine zipper was designed to enhance the formation of the disulfide bond, employing computer modeling to optimize amino acid interactions and resulting in a successful synthesis of the target peptide.
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Unlabelled: Air-liquid interface rings were observed on the side walls of stainless steel buffer vessels after certain downstream buffer preparations. Those rings were resistant to regular cleaning-in-place procedures but could be removed by manual means. To investigate the root cause of this issue, multiple analytical techniques, including liquid chromatography with tandem mass spectrometry detection (LC-MS/MS), high-resolution accurate mass liquid chromatography with mass spectrometry, nuclear magnetic resonance, Fourier transform infrared spectroscopy, and scanning electron microscopy with energy-dispersive X-ray spectroscopy have been employed to characterize the chemical composition of air-liquid interface rings.

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As part of the process-characterization campaign of a candidate vaccine product, a recently developed class of three-level designs-definitive-screening designs-was employed to select a quadratic model that describes the effect of six input process parameters, including protein concentration, formaldehyde-to-protein ratio, lysine concentration, reaction duration, pH, and reaction temperature, on a formylation protein-crosslinking reaction. This design requires only 17 experimental runs. The resulting model was then used to simulate 10,000 runs that account for the variability in the inputs expected on manufacturing scale.

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