Author/Authors :
Bruno H. Muller، نويسنده , , Alexandra Savatier، نويسنده , , Guillaume LʹHostis، نويسنده , , Narciso Costa، نويسنده , , Marc Bossus، نويسنده , , Sandrine Michel، نويسنده , , Catherine Ott، نويسنده , , Laurence Becquart، نويسنده , , Alain Ruffion، نويسنده , , Enrico A. Stura، نويسنده , , Frédéric Ducancel، نويسنده ,
Abstract :
Prostate-specific antigen (PSA) is a serum marker that is widely used for the diagnosis of prostatic diseases. Various subforms of free PSA, which are associated with prostate cancer differently, have been identified in sera. Thus, specific detection of certain subforms could permit discrimination between benign and malignant cases. Although the monoclonal antibody 5D3D11 displays the desired selectivity, its relative weak binding affinity prevents its development into an effective diagnostic tool. The directed-evolution strategy presented here succeeds in enhancing affinity and immunoassay sensitivity while maintaining selectivity.
Keywords :
affinity engineering , hot spots , phage-display , scFv antibody fragment , prostate-specific antigen