Please RSVP to Sergio Nanita - Sergio.c.nanita@usa.dupont.com - by Tuesday, May 7th, 2013.
An RSVP is needed to get a headcount for the served dinner.
Please note: If you are using a GPS locater, please enter 629 County Line Road, Radnor, PA 19087 or Latitude 40.05 and Longitude -75.35.
Mass spectrometry (MS) has become the darling of these efforts; the premise being that bigger, faster, higher resolution MS instruments can solve anything. But before becoming a carpenter with a magic hammer, it is worth looking at the nails we are trying to drive. The structure of many “biomarkers” for example has only been inferred by the presence of an ion. It is probably necessary to define the structure of the parent molecule from which the ion was derived. A second problem is in showing that molecular features targeted by analytical systems are either the same or co-reside with structural features that signifying disease. They may not associated. Being able to show that “analytical features” and “biological activity” of molecules are connected by multiple, high selectivity means is essential. A third problem is how to deal with the fact that sample complexity can exceed the limits of analytical tools. How separation systems can be used to reduce sample complexity, achieve targeted multiplexing, enhance detection sensitivity, and increase the confidence of identifications will be addressed. Finally there is the problem that MS can identify biomarkers in msec while sample preparation takes hours. This is a serious limitation not solved by large scale parallel processing. Early studies focusing on solutions to sample preparation will be presented. Finally, it will be suggested in conclusion that the ability to target multiple structures will be a dominant issue in the future of life science oriented separation systems.
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Last Updated April 10, 2013