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World J Gastroenterol. Dec 7, 2010; 16(45): 5752-5758
Published online Dec 7, 2010. doi: 10.3748/wjg.v16.i45.5752
Published online Dec 7, 2010. doi: 10.3748/wjg.v16.i45.5752
Figure 4 Enzyme activity assay of recombinant hepatitis B virus polymerase.
Comparison of enzyme activities between hepatitis B virus polymerase (HBV-Pol) from Escherichia coli expression system (P-E) and in vitro expression system (P-R). DNA-dependent DNA polymerase (DDDP) activity and RNA-dependent DNA polymerase (RDDP) activity of the P-E and P-R were monitored under standard conditions. All endogenous DDDP activities were suppressed by 60 mmol/L aphidicolin and 1 mmol/L NEM (A and B). The effects of increasing concentrations of adenosine triphosphate (ATP) are shown in C. DDDP activity using poly (dA) • oligo (dT)12-18 and RDDP activity using poly (rA) • oligo (dT)12-18 were used as the substrate for DDDP activity and RDDP activity assays, respectively. CPM: Counts per minute.
- Citation: Yu Y, Pandeya DR, Liu ML, Liu MJ, Hong ST. Expression and purification of a functional human hepatitis B virus polymerase. World J Gastroenterol 2010; 16(45): 5752-5758
- URL: https://www.wjgnet.com/1007-9327/full/v16/i45/5752.htm
- DOI: https://dx.doi.org/10.3748/wjg.v16.i45.5752