(1) Center for Infectious Disease Research and Vaccinology, South Dakota State University, Box 2175, 1119 North Campus Drive, Brookings, SD 57007, USA;(2) LI-COR Biosciences, Lincoln, NE 68504, USA
Abstract:
Detection of phosphoproteins plays an important role in understanding protein function in cellular signalling pathways. Improved
methods for identification and quantification of phosphoproteins are research priorities. Near-infrared (NIR) fluorescence
detection of a γ-modified ATP-biotin analog was used to detect protein phosphorylation, using both model kinase substrates
and mammalian cell lysates. NIR signal intensity was dependent on substrate and ATP-biotin concentrations.