Publications by authors named "Fabio Zurlo"

Protein-based biopharmaceutical drugs, such as monoclonal antibodies, account for the majority of the best-selling drugs globally in recent years. For bioprocesses, key performance indicators are the concentration and aggregate level for the product being produced. In water NMR (NMR), the use of the water transverse relaxation rate [(HO)] has been previously used to determine protein concentration and aggregate level; however, it cannot be used to separate between them without using an additional technique.

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When expressing complex biotherapeutic proteins, traditional expression plasmids and methods may not always yield sufficient levels of high-quality product. High-strength viral promoters commonly used for recombinant protein (rProtein) production in mammalian cells allow for maximal expression, but provide limited scope to alter their transcription dynamics. However, synthetic promoters designed to provide tunable transcriptional activity offer a plasmid engineering approach to more precisely regulate product quality, yield or to reduce product related contaminants.

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Host cell proteins (HCP) that co-purify with biologics produced in Chinese hamster ovary cells have been shown to impact product quality through proteolytic degradation of recombinant proteins, leading to potential product losses. Several problematic HCPs can remain in the final product even after extensive purification. Each recombinant cell line has a unique HCP profile that can be determined by numerous upstream and downstream factors, including clonal variation and the protein sequence of the expressed therapeutic molecule.

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The manufacture of bispecific antibodies by Chinese hamster ovary (CHO) cells is often hindered by lower product yields compared to monoclonal antibodies. Recently, reactive oxygen species have been shown to negatively impact antibody production. By contrast, strategies to boost cellular antioxidant capacity appear to be beneficial for recombinant protein expression.

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The role of the cerebellum in Alzheimer's disease (AD) has been neglected for a long time. Recent studies carried out using transgenic mouse models have demonstrated that amyloid-β (Aβ) is deposited in the cerebellum and affects synaptic transmission and plasticity, sometimes before plaque formation. A wide variability of motor phenotype has been observed in the different murine models of AD, without a consistent correlation with the extent of cerebellar histopathological changes or with cognitive deficits.

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Article Synopsis
  • - Numerous studies have shown that the cerebellum experiences both structural and functional changes in Alzheimer's disease, and this study focuses on early alterations in TgCRND8 mice before significant plaque formation.
  • - Behavioral tests demonstrated notable motor coordination and balance issues in 2-month-old TgCRND8 mice, along with patch-clamp recordings indicating dysfunction in cerebellar synapses caused by amyloid precursor protein overexpression.
  • - The study identified increased expression of specific proteins linked to oxidative stress in the cerebellum, suggesting a feedback loop that enhances reactive oxygen species production, potentially worsening Alzheimer's disease pathology in its early stages.
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