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ItemDetection of Active Caspases During Apoptosis Using Fluorescent Activity-Based ProbesEdgington-Mitchell, LE ; Bogyo, M ; Puthalakath, H ; Hawkins, CJ (HUMANA PRESS INC, 2016-01-01)Activity-based probes (ABPs) are reactive small molecules that covalently bind to active enzymes. When tagged with a fluorophore, ABPs serve as powerful tools to investigate enzymatic activity across a wide variety of applications. In this chapter, we provide detailed methods for using fluorescent ABPs to detect the activity of caspases during the onset of apoptosis in vitro. We describe how these probes can be used to biochemically profile caspase activity in vitro using fluorescent SDS-PAGE as well as their application to imaging protease activity in live animals and tissues.
ItemLive Cell Imaging and Profiling of Cysteine Cathepsin Activity Using a Quenched Activity-Based ProbeEdgington-Mitchell, LE ; Bogyo, M ; Verdoes, M ; Overkleeft, HS ; Florea, BI (HUMANA PRESS INC, 2017-01-01)Since protease activity is highly regulated by structural and environmental influences, the abundance of a protease often does not directly correlate with its activity. Because in most of the cases it is the activity of a protease that gives rise to its biological relevance, tools to report on this activity are of great value to the research community. Activity-based probes (ABPs) are small molecule tools that allow for the monitoring and profiling of protease activities in complex biological systems. The class of fluorescent quenched ABPs (qABPs), being intrinsically "dark" and only emitting fluorescence after reaction with the target protease, are ideally suited for imaging techniques such as small animal noninvasive fluorescence imaging and live cell fluorescence microscopy. An additional powerful characteristic of qABPs is their covalent and irreversible modification of the labeled protease, enabling in-depth target characterization. Here we describe the synthesis of a pan-cysteine cathepsin qABP BMV109 and the application of this probe to live cell fluorescence imaging and fluorescent SDS-PAGE cysteine cathepsin activity profiling.
ItemCSK-Homologous Kinasevan Roy, F ; Nimmrich, V ; Bespalov, A ; Möller, A ; Hara, H ; Turowec, JP ; St. Denis, NA ; Litchfield, DW ; Boucher, D ; Denault, J-B ; Matsuda, K ; Yuzaki, M ; Repeke, C ; Garlet, T ; Trombone, AP ; Garlet, G ; Repeke, C ; Garlet, T ; Silveira, EM ; Garlet, G ; Garlet, T ; Repeke, C ; Vieira, A ; Cunha, F ; Garlet, G ; Kubota, S ; Takigawa, M ; Soares, H ; Nolasco, S ; Gonçalves, J ; Bensussan, A ; Marie-Cardine, A ; Deswal, S ; Schamel, WWA ; Santos-Argumedo, L ; Deswal, S ; Schamel, WWA ; Bishop, GA ; Decker, DA ; Hostager, BS ; Bravo-Adame, ME ; Sandoval-Hernandez, MA ; Migueles-Lozano, OA ; Rosenstein, Y ; Johnson, P ; Samarakoon, A ; Saunders, AE ; Harder, KW ; Roberts, DD ; Soto-Pantoja, DR ; Isenberg, JS ; Lazo, PA ; Barcia, R ; Wu, H-J ; Muthusamy, N ; Bondada, S ; Levy, S ; Pawaria, S ; Binder, RJ ; Masai, H ; Hu, D ; Lahti, JM ; Singer, BB ; Horuk, R ; Miller, LJ ; Morisset, J ; Litchfield, DW ; Mistry, AR ; O’Callaghan, CA ; Fenton-May, AE ; O’Callaghan, CA ; Mistry, AR ; O’Callaghan, CA ; Reschen, M ; O’Callaghan, CA ; Willment, JA ; Brown, GD ; Rabinow, L ; Ness, SA ; Creutz, CE ; Yagishita-Kyo, N ; Inoue, M ; Nonaka, M ; Okuno, H ; Bito, H ; Okada, M ; Cheng, H-C ; Hossain, MI ; Kamaruddin, MA ; Chong, Y-P ; Sen, B ; Johnson, FM ; Pino, PA ; Cardona, AE ; Paroni, F ; Maedler, K ; Poon, RYC (Springer New York, 2012)