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Our hypothesis was that, in the case of large biomolecules, the changes of molecular conformation caused by the pressure or high flow rates (thermal effects) will play a much more important role in changing retention and selectivity. Especially when considering their “bind and elute” type retention behavior. In our work, this huge conformational change was experimentally verified both by fluorescence emission measurements and by the analysis of native and reduced forms of various proteins which possess the same molecular weight but a different conformation.
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Finally, a substantial effect was observed and demonstrated that the operating pressure is a useful click here method variable to adjust selectivity of large molecule separations.
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We are also involved in the development of new column designs and stationary phases which we believe will change the current practice of protein chromatography.
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