Author/Authors :
Roman C. Hillig، نويسنده , , Stefanie Urlinger، نويسنده , , J?rg Fangh?nel، نويسنده , , Bodo Brocks، نويسنده , , Cornelia Haenel، نويسنده , , Yvonne Stark، نويسنده , , Detlev Sülzle، نويسنده , , Dmitri I. Svergun، نويسنده , , Siegfried Baesler، نويسنده , , Guido Malawski، نويسنده , , Dieter Moosmayer، نويسنده , , Andreas Menrad، نويسنده , , Michael Schirner، نويسنده , , Kai Licha، نويسنده ,
Abstract :
Molecular interactions between near-IR fluorescent probes and specific antibodies may be exploited to generate novel smart probes for diagnostic imaging. Using a new phage display technology, we developed such antibody Fab fragments with subnanomolar binding affinity for tetrasulfocyanine, a near-IR in vivo imaging agent. Unexpectedly, some Fabs induced redshifts of the dye absorption peak of up to 44 nm. This is the largest shift reported for a biological system so far. Crystal structure determination and absorption spectroscopy in the crystal in combination with microcalorimetry and small-angle X-ray scattering in solution revealed that the redshift is triggered by formation of a Fab dimer, with tetrasulfocyanine being buried in a fully closed protein cavity within the dimer interface. The derived principle of shifting the absorption peak of a symmetric dye via packaging within a Fab dimer interface may be transferred to other diagnostic fluorophores, opening the way towards smart imaging probes that change their wavelength upon interaction with an antibody.
Keywords :
Diagnostic Imaging , crystal structure , cyanine dye , Isothermal titration calorimetry , Small-Angle X-Ray Scattering