Active Site Plasticity of a Computationally Designed Retro‐Aldolase Enzyme. Issue 4 (3rd March 2014)

• Record Type: Journal Article
• Authors: Obexer, Richard; Studer, Sabine; Giger, Lars; Pinkas, Daniel M.; Grütter, Markus G.; Baker, David; Hilvert, Donald
• Is Part Of: ChemCatChem. Volume 6:Issue 4(2014:Apr.)
• Page Start: 1043
• Page End: 1050
• Publication Date: 2014-03-03
• Subjects: Catalysis -- Periodicals; 541.39505
• DOI: 10.1002/cctc.201300933
• Languages: English
• ISSNs: 1867-3880

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>RA110 is a computationally designed retro‐aldolase enzyme that utilizes amine catalysis to convert 4‐hydroxy‐4‐(6‐methoxy‐2‐naphthyl)‐2‐butanone to 6‐methoxy‐2‐naphthaldehyde and acetone. The original design accelerated substrate cleavage by a factor of 12 000 over background, and its activity was subsequently increased more than a thousand‐fold by directed evolution. The X‐ray structure of the evolved catalyst covalently modified with a 1, 3‐diketone inhibitor deviates substantially from the design model, however, with the ligand adopting a completely different orientation than predicted. Moreover, significant activity was maintained even after relocation of the reactive lysine within the apolar binding pocket. These results suggest that the success of the original design is not ascribable to atomically accurate molecular recognition, but rather to successful placement of a reactive lysine adjacent to an apolar binding pocket. Nevertheless, the stabilizing interactions observed at the active site of the evolved variant suggest that improvements in the precision of design calculations will afford enzymes with higher catalytic activities.</p> </abstract>