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|dc.title||Multicolor, one- and two-photon imaging of enzymatic activities in live cells with fluorescently quenched activity-based probes (qABPs)|
|dc.identifier.citation||Hu, M., Li, L., Wu, H., Su, Y., Yang, P.-Y., Uttamchandani, M., Xu, Q.-H., Yao, S.Q. (2011-08-10). Multicolor, one- and two-photon imaging of enzymatic activities in live cells with fluorescently quenched activity-based probes (qABPs). Journal of the American Chemical Society 133 (31) : 12009-12020. ScholarBank@NUS Repository. https://doi.org/10.1021/ja200808y|
|dc.description.abstract||Fluorescence imaging provides an indispensable way to locate and monitor biological targets within complex and dynamic intracellular environments. Of the various imaging agents currently available, small molecule-based probes provide a powerful tool for live cell imaging, primarily due to their desirable properties, including cell permeability (as a result of their smaller sizes), chemical tractability (e.g., different molecular structures/designs can be installed), and amenability to imaging a wide variety of biological events. With a few exceptions, most existing small molecule probes are however not suitable for in vivo bioimaging experiments in which high-resolution studies of enzyme activity and localization are necessary. In this article, we reported a new class of fluorescently Quenched Activity-Based Probes (qABPs) which are highly modular, and can sensitively image (through multiple enzyme turnovers leading to fluorescence signal amplification) different types of enzyme activities in live mammalian cells with good spatial and temporal resolution. We have also incorporated two-photon dyes into our modular probe design, enabling for the first time activity-based, fluorogenic two-photon imaging of enzyme activities. This, hence, expands the repertoire of smart, responsive probes currently available for live cell bioimaging experiments. © 2011 American Chemical Society.|
|dc.description.sourcetitle||Journal of the American Chemical Society|
|Appears in Collections:||Staff Publications|
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