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. 2008 Aug 29;283(35):24089–24102. doi: 10.1074/jbc.M803422200

TABLE 2.

Summary of replication assays results

Mean values from each set of replicate experiments are shown, normalized to the median activity value of either wild-type HCV NS5B polymerase or adaptive Con1/luc HCV replicon controls. In each case, the standard deviation value was less than 10% of the median activity value.

Mutation in RdRp RdRp activitya Mutation effect Con1/luc activityb Mutation effect Phenotypec
%WT %WT
T92S 18 Down 4 Down I
P93A 90 WT-like 67 WT-like I
P94A 115 WT-like 0 Null II
H95S 104 WT-like 0 Null II
S96T 82 WT-like 0 Null II
A97S 88 WT-like 0 Null II
R98K 157 Up 0 Null II
R98I 68 WT-like 0 Null II
S99T 0 Null 0 Null I
K100I 20 Down 0 Null II
F101Y 134 Up 0 Null II
F101A 89 WT-like 0 Null II
G102A 32 Down 3 Down I
Y103F 89 WT-like 98 WT-like I
G104A 146 Up 125 WT-like NA
A105S 62 WT-like 60 WT-like I
WT 100 WT 100 WT I
D318N 0 Null 0 Null I
a

The results of standard primer-dependent RdRp assays obtained with purified mutated enzymes are shown.

b

The results of transient replication assay obtained with mutated Con1/luc replicons (144 h post-transfection).

c

For phenotype I, the mutation results in the same effect in both assays (up/up, WT-like/WT-like, down/down, or null/null mutations). For phenotype II, the mutation is non-null in primer-dependent RdRp assay and null in transient replication assay; NA indicates not applicable.