High-Throughput Screens Based on NAD(P)H Depletion
Screening conditions should simulate the final application as closely as possible. This is especially a challenge when chromophore-free (e.g., aliphatic) substrates are used and no simple and reliable high-throughput method for quantitative analysis of the respective reaction product is available. The screening procedure should also be generally applicable for a certain class of enzymes. Generation of “surrogate substrates” by derivatization with chromogenic groups can have a negative effect on enzyme development by directed evolution, e.g., by causing a change in substrate specificity.
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Monitoring Rapid Endocytosis in the Electron Microscope via Photoconversion of Vesicles Fluorescentl
Cells communicate via endo- and exocytosis with their enviro...
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Analysis of Phosphoinositide Dynamics During Phagocytosis Using Genetically Encoded Fluorescent Bios
Phosphoinositide signaling is essential for successful phago...