Annamaria Lilienkampf

Find an error

Name:
Organization: The University of Edinburgh , England
Department:
Title: (PhD)
Co-reporter:Martha Mackay, Ana M. Pérez-López, Mark Bradley and Annamaria Lilienkampf  
Molecular BioSystems 2016 vol. 12(Issue 3) pp:693-696
Publication Date(Web):08 Dec 2015
DOI:10.1039/C5MB00730E
11 FRET-based fluorogenic substrates were constructed using the pentapeptide template Asp-Glu-X2-Asp-X1′, and evaluated with caspase-3, caspase-7 and cathepsin B. The sequence Asp-Glu-Pro-Asp-Ser was able to selectively quantify caspase-3 activity in vitro without notable caspase-7 and cathepsin B cross-reactivity, while exhibiting low μM KM values and good catalytic efficiencies (7.0–16.9 μM−1 min−1).
Benzenamine, 2-methoxy-5-[1-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazol-4-yl]-
Benzene, 5-azido-1,2,3-trimethoxy-
2-CHLORO-4-(3-PYRIDINYL)BENZOIC ACID
Polyethylene glycol 200 diacrylate
2-(6-Amino-3-imino-3H-xanthen-9-yl)benzoic acid hydrochloride
Benzenamine, 5-ethynyl-2-methoxy-
Caspase-3
2H-1-Benzopyran-2-one, 3-azido-7-hydroxy-