Synthesis, solution and crystal structure of the coenzyme B12 analogue Coβ-2′-fluoro-2′,5′-dideoxyadenosylcobalamin

• Synthesis of Coβ-2′-fluoro-2′,5′-dideoxyadenosylcobalamin, lacking the critical 2′-OH group
• Solution structure of 2′FAdoCbl has similar features as that of coenzyme B12 (AdoCbl).
• Crystal structure of 2′FAdoCbl is similar to the structure of AdoCbl in the crystal.
• First coenzyme B12 analogue with 19F-label in the organometallic moiety for 19F NMR

Crystal structure analyses have helped to decipher the mode of binding of coenzyme B12 (AdoCbl) in the active site of AdoCbl-dependent enzymes. However, the question of how such enzymes perform their radical reactions is still incompletely answered. A pioneering study by Gruber and Kratky of AdoCbl-dependent glutamate mutase (GLM) laid out a path for the movement of the catalytically active 5′-deoxyadenosyl radical, in which H-bonds between the protein and the 2′- and 3′-OH groups of the protein bound AdoCbl would play a decisive role. Studies with correspondingly modified coenzyme B12-analogues are of interest to gain insights into cofactor binding and enzyme mechanism. Here we report the preparation of Coβ-2′-fluoro-2′,5′-dideoxyadenosylcobalamin (2′FAdoCbl), which lacks the 2′-OH group critical for the interaction in enzymes. 2′FAdoCbl was prepared by alkylation of cob(I)alamin, obtained from the electrochemical reduction of aquocobalamin. Spectroscopic data and a single crystal X-ray analysis of 2′FAdoCbl established its structure, which was very similar to that one of coenzyme B12. 2′FAdoCbl is a 19F NMR active mimic of coenzyme B12 that may help to gain insights into binding interactions of coenzyme B12 with AdoCbl-dependent enzymes, proteins of B12 transport and of AdoCbl-biosynthesis, as well as with B12-riboswitches.

A coenzyme B12 mimic carrying a 19F-label is presented and suggested useful for studies with B12-dependent enzymes.Figure optionsDownload as PowerPoint slide