Appeal No. 2002-2281 Page 4 Application No. 08/302,423 the full length V antigen, the vaccine or composition must contain the antigen encoded by the construct illustrated in Figure 1. Upon review of the Answer, and the references relied upon by the examiner, we are unable to identify any suggestion to utilize a truncated Y. pestis antigen, one that is missing 67 amino acids of the N-terminal end. See also, Brief, pages 5 and 6. While the examiner believes that “the burden is upon [a]pplicant to demonstrate that the resulting peptide produces a materially, functionally and structurally different protein,” for the forgoing reasons we believe that this evidence is already of record. What is not of record, is any evidence suggesting that a person of ordinary skill in the art at the time the invention was made would have been motivated to utilize a truncated antigenic protein, having the characteristics of the one encoded by the construct illustrated in appellants’ Figure 1 as is required by the claimed invention. Prima facie obviousness based on a combination of references requires that the prior art provide “a reason, suggestion, or motivation to lead an inventor to combine those references.” Pro-Mold and Tool Co. v. Great Lakes Plastics, Inc., 75 F.3d 1568, 1573, 37 USPQ2d 1626, 1629 (Fed. Cir. 1996). [E]vidence of a suggestion, teaching, or motivation to combine may flow from the prior art references themselves, the knowledge of one of ordinary skill in the art, or, in some cases, from the nature of the problem to be solved. . . . The range of sources available, however, does not diminish the requirement for actual evidence. That is, the showing must be clear and particular. In re Dembiczak, 175 F.3d 994, 999, 50 USPQ2d 1614, 1617 (Fed. Cir. 1999) (citations omitted). The suggestion to combine prior art references must comePage: Previous 1 2 3 4 5 6 NextLast modified: November 3, 2007