6 research outputs found
Observation of Small Cluster Formation in Concentrated Monoclonal Antibody Solutions and Its Implications to Solution Viscosity
AbstractMonoclonal antibodies (mAbs) are a major class of biopharmaceuticals. It is hypothesized that some concentrated mAb solutions exhibit formation of a solution phase consisting of reversibly self-associated aggregates (or reversible clusters), which is speculated to be responsible for their distinct solution properties. Here, we report direct observation of reversible clusters in concentrated solutions of mAbs using neutron spin echo. Specifically, a stable mAb solution is studied across a transition from dispersed monomers in dilute solution to clustered states at more concentrated conditions, where clusters of a preferred size are observed. Once mAb clusters have formed, their size, in contrast to that observed in typical globular protein solutions, is observed to remain nearly constant over a wide range of concentrations. Our results not only conclusively establish a clear relationship between the undesirable high viscosity of some mAb solutions and the formation of reversible clusters with extended open structures, but also directly observe self-assembled mAb protein clusters of preferred small finite size similar to that in micelle formation that dominate the properties of concentrated mAb solutions
Including organic mixture influence on dioxins and furans fate for toxic impact assessment in a life cycle context
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Discrimination of Flavonoids and Red Wine Varietals by Arrays of Differential Peptidic Sensors
The chemical structures and concentrations of an organism's natural products are dependent upon its genome and environmental factors. Examples are the complex metabolite solutions resulting from plant and fermentation processes. Here, we describe sensor arrays composed of supramolecular ensembles that undergo indicator displacement and discriminate selected flavonoids and mixtures thereof: wine varietals. Changes in UV-vis absorbance upon indicator displacement in the array were analyzed using pattern recognition protocols. The flavonoids were differentiated in terms of structure and concentration, while red wines were generally classified by varietals, even from different vintners. The technique highlights the power of differential sensor arrays to classify mixtures by metabolite distribution, even when the natural products are not known.National Science Foundation CHE-0716049Welch Foundation F-1151Chemistr
Including organic mixture influence on dioxins and furans fate for toxic impact assessment in a life cycle context
CDK4/6 inhibition reprograms the breast cancer enhancer landscape by stimulating AP-1 transcriptional activity
Pharmacologic inhibitors of cyclin-dependent kinases 4 and 6 (CDK4/6) were designed to induce cancer cell cycle arrest. Recent studies have suggested that these agents also exert other effects, influencing cancer cell immunogenicity, apoptotic responses, and differentiation. Using cell-based and mouse models of breast cancer together with clinical specimens, we show that CDK4/6 inhibitors induce remodeling of cancer cell chromatin characterized by widespread enhancer activation, and that this explains many of these effects. The newly activated enhancers include classical super-enhancers that drive luminal differentiation and apoptotic evasion, as well as a set of enhancers overlying endogenous retroviral elements that is enriched for proximity to interferon-driven genes. Mechanistically, CDK4/6 inhibition increases the level of several Activator Protein-1 (AP-1) transcription factor proteins, which are in turn implicated in the activity of many of the new enhancers. Our findings offer insights into CDK4/6 pathway biology and should inform the future development of CDK4/6 inhibitors