Appeal 2007-1824 Application 10/639,718 microspot1 of the array and unlabeled target which competes with the labeled cognate ligands for binding sites on the array (Lahiri 6: ¶ 0081). Therefore, Lahiri teaches the step of contacting a cocktail solution with an array in the presence of a target compound. According to Lahiri, the affinity of the target for the probe microspot relative to the labeled ligand is determined by the decrease in the amount of binding of the labeled ligand. But for the specific affinity, specificity, and cross-reactivity of the cognate ligands, Lahiri teaches the method set forth in Appellants’ claim 1. The Examiner relies on Matray and Jordan to make up for this deficiency in Lahiri. Specifically, the Examiner finds that Matray “teaches a plurality of specific binding pairs, each having a dissociation constant of 1 nM, in order to provide high affinity between the binding partner and analyte in assays to simultaneously detect a plurality of analytes in a sample. See column 3, lines 43-44 and column 13, lines 9-23” (Answer 6). In addition, the Examiner finds that Jordan “teaches highly selective ligands that eliminate any possibility of cross-reactivity between receptor types, in order to understand GPCR dimerization in a specific compound receptor field and to clarify the mechanism of the compounds towards the development of novel 1 Clearly, to perform a competitive assay on an array comprising microspots of different proteins, the labeled cognate ligands must be capable of binding to each protein microspotted to the substrate. To do otherwise would defeat the intended purpose of the competitive binding assay. See KSR Int’l Co. v. Teleflex Inc., 127 S. Ct. 1727, 1741, 82 USPQ2d 1385, 1396 (2007) (It is proper to “take account of the inferences and creative steps that a person of ordinary skill in the art would employ.”). See also id. at 1742, 82 USPQ2d at 1397 (“A person of ordinary skill is also a person of ordinary creativity, not an automaton.”). 5Page: Previous 1 2 3 4 5 6 7 8 9 10 Next
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