The use of light to reversibly change the structure of biologically relevant molecules and turn "on" and "off" important biochemical functions "on-command" offers the biomedical end-user a non-invasive, rapid, reversible, spatial and temporal tool for research and therapy. Applying this control strategy to macromolecules such as oligonucleotides and proteins is challenging because their large size and complexity makes it difficult to target a particular area on the macromolecules for modification, although several impressive examples have been reported. [1][2][3][4][5][6][7][8][9][10][11][12][13][14] The alternative is the use of photoresponsive small molecules that play an intimate role in biochemical processes, as either cofactors or inhibitors. Not only would these molecular systems be easier to photoactivate and deactivate than their enzyme partners, they would also provide a more "universal" method to regulate biological function because the same cofactor can be involved in more than one operation.We have recently described how two different colors of light can be used to convert a small molecule between two isomeric forms differing by an order of magnitude in their ability to act as an inhibitor for human carbonic anhydrase. [15] While regulating inhibitors is appealing, [16][17][18] applying the same strategy to enzyme cofactors would provide control over a more diverse set of biochemical systems. Cofactors have all the earmarks of a suitable photoresponsive target. They tend to be small in size, structurally simple and easy to modify and study, while still allowing for ultimate control over the enzyme activity. Here, we take a first logical step by using a well-known enzyme cofactor as the inspiration in our design of a proof-of-concept demonstration. We show how our biomimetic system acts as a photoswitchable catalyst for a biochemical reaction. [19] The biologically active form of vitamin B 6 , pyridoxal 5'phosphate (PLP), is a versatile enzyme cofactor responsible for amino acid metabolism in all organisms from bacteria to humans. [20] Its participation in a diverse range of enzymatic reactions including transamination, racemization, decarboxylation, and numerous elimination and replacement processes makes it unrivalled. [21] It is a particularly inspiring cofactor for our proof-of-concept design because it can catalyze many processes without the presence of an enzyme. [22,23] It is also the role-model target of the studies described in this report.The structural features responsible for the action of PLP are the aldehyde and pyridinium functional groups, which are electronically connected to each other through bonds (Scheme 1). This intimate connectivity allows any molecule attached to the aldehyde to "sense" the electron withdrawing nature of the positively charged heterocycle. An example of this is the aldimine generated when an amino acid condenses with PLP (Scheme 1) and it is this Schiff base that is responsible for the enormous range of reactions the cofactor catalyzes. [24] The pyridinium group...