Citation:
CUI Xiu-Yun, SUN Ning-Ning, XIE Xiao-Na, SUN Wan-Chun, ZHAO Qing, LIU Ning. Detection of Newly Synthesized Proteins via Metabolic Incorporation of Non-Natural Amino Acid[J]. Chinese Journal of Analytical Chemistry,
;2018, 46(11): 1808-1813.
doi:
10.11895/j.issn.0253-3820.171035
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A method for detection of newly synthesized protein via metabolic incorporation of non-natural amino acid was developed, in which Raw264.7 cells were treated by lipopolysaccharide (LPS) to generate tumor necrosis factor alpha (TNF-α). Experimental parameters including the concentration of LPS and the duration of LPS treatment were investigated by measuring the LPS stimulated TNF-α from Raw264.7 cells. The optimal experimental conditions were determined as follows. Raw264.7 cells were cultured in Met-free DMEM containing 1% fetal bovine serum (FBS), and then treated for 4 h with LPS at concentration of 10 ng/mL in presence of AHA. The biotin tags were introduced into proteins containing azidohomoalanine (AHA) by copper-catalyzed alkyne-azidecycloaddition (CuAAC). Then TNF-α was specifically captured by the antibody adsorbed on the solid support, on which the biotin tag could be detected by streptavidin coupled with horseradish peroxidase (HRP). This study provided a method for the detection of a specific newly synthesized protein, and characterization of specific protein turnover.
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