Title of article :
Catalysis of decarboxylation by a preorganized heterogeneous microenvironment: crystal structures of abzyme 21D8
Author/Authors :
Kinya Hotta، نويسنده , ,
Holger Lange، نويسنده , , Dean J. Tantillo، نويسنده , , K.N Houk، نويسنده , , Donald Hilvert، نويسنده , , Ian A. Wilson، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2000
Abstract :
Antibody 21D8 catalyzes the solvent-sensitive decarboxylation of 3-carboxybenzisoxazoles. The crystal structure of chimeric Fab 21D8 with and without hapten at 1.61 Å and 2.10 Å, respectively, together with computational analysis, shows how a melange of polar and non-polar sites are exploited to achieve both substrate binding and acceleration of a reaction normally facilitated by purely aprotic dipolar media. The striking similarity of the decarboxylase and a series of unrelated esterase antibodies also highlights the chemical versatility of structurally conserved anion binding sites and the relatively subtle changes involved in fine-tuning the immunoglobulin pocket for recognition of different ligands and catalysis of different reactions.
Keywords :
antibody catalysis , immune response , Computational docking , enzyme evolution , medium effects
Journal title :
Journal of Molecular Biology
Journal title :
Journal of Molecular Biology