Masking the Peroxidase‐Like Activity of the Molybdenum Disulfide Nanozyme Enables Label‐Free Lipase Detection

Abstract Two‐dimensional MoS 2 nanoparticles (2D‐nps) exhibit artificial enzyme properties that can be regulated at bio‐nanointerfaces. We discovered that protein lipase is able to tune the peroxidase‐like activity of MoS 2 2D‐nps, offering low‐nanomolar, label‐free detection and identification in samples with unknown identity. The inhibition of the peroxidase‐like activity of the MoS 2 2D‐nps was demonstrated to be concentration dependent, and as low as 5 n m lipase was detected with this approach. The results were compared with those obtained with several other proteins that did not display any significant interference with the nanozyme behavior of the MoS 2 2D‐nps. This unique response of lipase was characterized and exploited for the successful identification of lipase in six unknown samples by using qualitative visual inspection and a quantitative statistical analysis method. The developed methodology in this approach is noteworthy for many aspects; MoS 2 2D‐nps are neither labeled with a signaling moiety nor modified with any ligands for signal readout. Only the intrinsic nanozyme activity of the MoS 2 2D‐nps is exploited for this detection approach. No analytical equipment is necessary for the visual detection of lipase. The synthesis of the water‐soluble MoS 2 2D‐nps is low costing and can be performed in bulk scale. Exploring the properties of 2D‐nps and their interactions with biological materials reveals highly interesting yet instrumental features that offer the development of novel bioanalytical approaches.