Ex Parte Donoho et al - Page 4


                  Appeal 2004-1103                                                                                              
                  Application 09/733,387                                                                                        
                  characterized Pb99 as a G-protein coupled receptor.  Therefore, we disagree                                   
                  with appellants’ assertion that Sleckman supports a conclusion that the sequence                              
                  of claim 1 must encode a G protein-coupled receptor because it shares some                                    
                  degree of similarity with Pb99.  Request, page 2.                                                             
                          Sleckman reports on the cloning and functional characterization of an                                 
                  early-lymphocyte-specific gene - Pb99.  See e.g., Sleckman title.  In this report,                            
                  Sleckman mentions G protein-coupled receptors three times.  First, Sleckman’s                                 
                  abstract states “[t]he cDNA with the longest open reading frame encodes a                                     
                  putative protein that has seven hydrophobic domains similar to those of seven                                 
                  membrane-spanning proteins, such as the classical G protein-coupled                                           
                  receptors.”  We do not find this statement to be a characterization of Pb99 as a G                            
                  protein-coupled receptor.  To the contrary, Sleckman is simply noting that Pb99                               
                  has seven hydrophobic domains which are similar to those in seven membrane-                                   
                  spanning proteins, for example, G protein-coupled receptors.  Similarly, in the                               
                  second column of page 4406, Sleckman restates that Pb99 “may be a seven-                                      
                  membrane-spanning protein similar to G protein-coupled                                                        
                  receptors . . . .”  In our opinion, this is far from a functional characterization of                         
                  Pb99 as a G protein-coupled receptor.  Finally, Sleckman states that Pb99                                     
                  “contains a hydrophobic signal peptide and seven distinct hydrophobic domains,                                
                  suggesting that it may be an integral membrane protein that spans the                                         
                  membrane seven times, similar to the classical G protein-coupled                                              
                  receptors. . . .”  Sleckman, page 4409, second column.  Again, it is our opinion                              
                  that this is far from a functional characterization of Pb99 as a G protein-coupled                            
                  receptor.                                                                                                     
                          Instead of functionally characterizing Pb99 as a G protein-coupled                                    
                  receptor, Sleckman recognizes that “Pb99 shares some homology with members                                    
                  of the recently described EGF-TM7 subfamily of cell surface receptors . . . .”  Id.                           
                  According to Sleckman, “it has been proposed that the EGF-TM7 proteins are                                    
                  receptors which function in the immune response . . . .  However, a clear role for                            
                  the EGF-TM7 receptors in the immune response has yet to be elucidated.”                                       
                  Sleckman, page 4409, column 2.  Lastly, Sleckman concludes that “[f]uture                                     


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