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Oster, M. E.

Publications and source records attributed to Oster, M. E..

2 recordsLinked to original sources

Validity and reliability of a new whole room indirect calorimeter to assess metabolic response to small-calorie loads

ObjectiveTo provide an overview of our whole room indirect calorimeter (WRIC), demonstrate validity and reliability of our WRIC, and explore a novel application of Bayesian hierarchical modeling to assess responses to small carbohydrate loads. MethodsSeven gas infusion studies were performed using a gas blender and profiles designed to mimic resting and postprandial metabolic events to assess WRIC validity. In a crossover design, 16 participants underwent fasting and postprandial measurements, during which they consumed a 75-kcal drink containing sucrose, dextrose, or fructose. Linear mixed effects models were used to compare resting and postprandial metabolic rate (MR) and CO (CO). Bayesian Hierarchical Modeling was also used to model postprandial CO trajectories for each participant and condition. ResultsMean total error in infusions were 1.27 {+/-} 1.16% and 0.42 {+/-} 1.21% for VO2 and VCO2 respectively, indicating a high level of validity. Mean resting MR was similar across conditions ([Formula] =1.05 {+/-} 0.03 kcal/min, p=0.82, ICC: 0.91). While MR increased similarly among all conditions ([~]13%, p=0.29), postprandial CO parameters were significantly lower for dextrose compared with sucrose or fructose. ConclusionsOur WRIC validation and novel application of statistical methods presented here provide important foundations for new research directions using WRIC.

physiology↗

Natural and designed proteins inspired by extremotolerant organisms can form condensates and attenuate apoptosis in human cells

Many organisms can survive extreme conditions and successfully recover to normal life. This extremotolerant behavior has been attributed in part to repetitive, amphipathic, and intrinsically disordered proteins that are upregulated in the protected state. Here, we assemble a library of approximately 300 naturally-occurring and designed extremotolerance-associated proteins to assess their ability to protect human cells from chemically-induced apoptosis. We show that several proteins from tardigrades, nematodes, and the Chinese giant salamander are apoptosis protective. Notably, we identify a region of the human ApoE protein with similarity to extremotolerance-associated proteins that also protects against apoptosis. This region mirrors the phase separation behavior seen with such proteins, like the tardigrade protein CAHS2. Moreover, we identify a synthetic protein, DHR81, that shares this combination of elevated phase separation propensity and apoptosis protection. Finally, we demonstrate that driving protective proteins into the condensate state increases apoptosis protection, and highlight the ability for DHR81 condensates to sequester caspase-7. Taken together, this work draws a link between extremotolerance-associated proteins, condensate formation, and designing human cellular protection.

synthetic biology↗