TABLE 1.
Sense primers used to introduce site-directed mutations into clone pMVE-1-51a
| Primer name | Sequenceb | Amino acid mutation |
|---|---|---|
| E-277-a-fwd | 5′-CAGTCGAGTTTTCGAGCATCACACTTAAACTCACTTCAG-3′ | E-277 Ser→Ile |
| E-277-b-fwd | 5′-CAGTCGAGTTTTCGAGCAACACACTTAAACTCACTTCAG-3′ | E-277 Ser→Asn |
| E-277-c-fwd | 5′-CAGTCGAGTTTTCGAGCGTCACACTTAAACTCACTTCAG-3′ | E-277 Ser→Val |
| E-277-d-fwd | 5′-CAGTCGAGTTTTCGAGCCCCACACTTAAACTCACTTCAG-3′ | E-277 Ser→Pro |
| E-390-a-fwd | 5′-TTGTGGTAGGCAGGGGAGAGAAGCAGATCAATCACCACT-3′ | E-390 Asp→Glu |
| E-390-b-fwd | 5′-TTGTGGTAGGCAGGGGAAACAAGCAGATCAATCACCACT-3′ | E-390 Asp→Asn |
| E-390-c-fwd | 5′-TTGTGGTAGGCAGGGGATACAAGCAGATCAATCACCACT-3′ | E-390 Asp→Tyr |
Antisense complementary primers (not shown) were used in combination with sense primers to form primer pairs for site-directed mutagenesis.
Nucleotide substitutions are underlined and affected codons are highlighted in bold.