Ex parte LEFKOWITZ et al. - Page 3




                 Appeal No.: 1996-1307                                                                          Paper No. 34                            
                 Application No.: 08/038,072                                                                               Page 3                       
                 phosphorylation of the $ AR by $ adrenergic receptor kinase                                                                            
                                                            2                                                                                           
                 ($ar kinase) (Lefkowitz at 4995 and Huganir at 474-475).                                                                               
                          The examiner states that "[t]he primary references do not                                                                     
                 teach inhibition of the phosphorylation by using an inhibitor                                                                          
                 of the kinase."   The examiner relies upon Appellants' "own3                                                                                                           
                 admissions" at page ten of Appellants' specification for                                                                               
                 teaching "known compounds capable of inhibiting receptor                                                                               
                 kinases involved in mediating homologous desensitization of                                                                            
                 adenylyl cyclase-coupled receptors"  (Paper No. 33 at 3).  The                                                                         
                 relevant disclosure at page ten of Appellants' specification                                                                           
                 is as follows:                                                                                                                         
                          Compounds suitable for use in the present invention                                                                           
                          include those capable of inhibiting receptor                                                                                  
                          kinases, for example, specific protein kinases                                                                                
                          involved in mediating homologous desensitization of                                                                           
                          adenylyl cyclase-coupled receptors (i.e. $ar                                                                                  
                          kinase).  (See also Blackshear (1988) FASEB J.                                                                                
                          2:2957; Middleton (1988) Ann. Allergy 61:53; Hunnan                                                                           
                          [sic, Hannun] (1988) Science 243:500.)                                                                                        

                                                                  DISCUSSION                                                                            



                          3Claim 15 requires inhibition of $ar kinase-induced                                                                           
                 phosphorylation which does not necessarily require inhibition                                                                          
                 of                                                                                                                                     
                 the kinase.  An agent capable of inhibiting the $ar kinase                                                                             
                 would be expected to inhibit phosphorylation of the receptor                                                                           
                 and in fact this does appear to be how the claimed invention                                                                           
                 works(Paper No. 1 (Specification) at 10).                                                                                              





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