Appeal 2007-1824 Application 10/639,718 INTRODUCTION The claims are directed to a method for identifying or evaluating target compounds (claims 1-17, 43, 44), a method to determine binding affinity of labeled ligands using microarrays (claim 18), a method for determining binding affinities between ligands and membrane proteins (claims 45 and 46), and a method for conducting protein array assays (claims 47-51). Claims 1 and 16 are illustrative: 1. A method for identifying or evaluating target compounds capable of modulating ligand-receptor interactions, the method comprising: a) providing a plurality of receptor microspots on a substrate to form an array; b) preparing a cocktail solution of labeled ligands, each labeled ligand having an affinity of from about 0.1 nM to about 20 nM and a specificity of at least 50% to bind with at least one corresponding paired receptor in said array and a cross activity of no more than 10% with receptors on said array other than said at least one corresponding paired receptor; c) contacting said cocktail solution with said array in the presence of a target compound; and d) detecting a level of binding between each said labeled ligand and its respective paired receptor, wherein a change in the level of binding between one of said labeled ligands and its respective paired receptor in the presence of said target compound, as compared to a control level of binding, is indicative that said target compound is capable of modulating the interaction between said one labeled ligand and its respective paired receptor. 16. The method according to claim 1, wherein said method comprises providing at least two receptors co-immobilized within a single microspot, in combination with a two-color detection technique, to at least double the capacity of probe elements. The Examiner relies on the following prior art references to show unpatentability: Bryen A. Jordan, “Opioids and Their Complicated Receptor Complexes,” Neuropsychopharmacology, 23(54), S5-S18 (2000). 2Page: Previous 1 2 3 4 5 6 7 8 9 10 Next
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