High throughtput screening of potential displacer molecules

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

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C530S412000, C530S415000, C530S416000, C530S344000, C210S198200, C210S635000, C210S656000

Reexamination Certificate

active

06881540

ABSTRACT:
An effective technique for the high throughput screening of displacers is described. In this technique, potential displacers are employed to displace a biomolecule (e.g., protein) adsorbed on a chromatographic resin in small-scale batch displacement experiments. The amount of protein displaced from a specific resin by a defined concentration of displacer is determined by monitoring the supermatant for the protein. By evaluating the displaced protein rather than the displacer itself, this technique enables a single detection technique (e.g., absorbance, fluorescence, etc.) to be employed for all batch displacement experiments. By monitoring the amount of protein displaced, the effacy of a large number of potential displacers can be rapidly evaluated. The entire experimental procedure can be carried out rapidly and is thus amenable to high throughput parallel screening of molecules possessing a large range of affinities and physico-chemical properties. The error of the technique is within 5% of protein displaced, thus making it a very reliable technique. The technique can be extended to different stationary phase materials, biomolecules, and modes of interaction.

REFERENCES:
patent: 5478924 (1995-12-01), Cramer et al.
patent: 5606033 (1997-02-01), Cramer et al.
patent: 6066848 (2000-05-01), Kassel et al.
Jayaraman, G.; Yu-Fei, L.; Moore, J. A.; Cramer, S. M. “Ion-exchange displacment chromatography of proteins. Dendritic polymers as novel displacers” Journal of Chromatography A 1995 702(1+2), 143-55.

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