TABLE 1.
Heterodimerb | Activity (%) |
---|---|
Wild type | 100 |
G190A | 170 |
G190S | 120 |
G190E | 20 |
L74V-G190E | 100 |
V75I-G190E | 105 |
L74V | 100 |
V75I | 100 |
Individual mutations were prepared in RT(66) clones (13, 17) by the method of BspMI cassette mutagenesis as previously described (2, 3). p66-p51 heterodimers were generated and purified as previously described (4). The polymerase assays were done as previously described (4). The reactions used equal amounts of purified p66-p51 heterodimers (2.0 ng) and poly(rC) · oligo(dG) as the substrate. The amount of labeled polymer collected for the wild-type heterodimer was considered 100% activity, and the amounts of labeled polymer collected for the various mutant heterodimers were normalized to this value.
The heterodimers other than the wild type are designated by the mutations they carry.