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Immobilization and electrical wiring of enzymes is of particular importance for the elaboration of efficient biosensors and can be cumbersome. Here, we report a fast and easy protocol for enzyme immobilization and as a proof of concept we applied it to the immobilization of Bilirubin Oxidase, a labile enzyme. In the first step, bilirubin oxidase is mixed with a redox hydrogel “wiring” the enzyme reaction centers to electrodes. Then, this adduct is covered by an outer layer of PEGDA made by photoinitiated polymerization of poly(ethylene-glycol) diacrylate (PEGDA) and a photoclivable precursor, DAROCUR®. This 2 steps protocol is 18 times faster than the current state-of-the-art protocol and leads to currents 25 % higher. In addition, the outer layer of PEGDA acts as a protective layer increasing the lifetime of the electrode by 100 % when operating continuously for 2000 s and by 60 % when kept in dry state for 24 hours. This new protocol is particularly appropriate for labile enzymes that quickly denaturate. In addition, by tuning the ratio PEGDA/DAROCUR®, it is possible to make the enzyme electrode even more active or more stable.