Novel mutations in Moloney Murine Leukemia Virus reverse transcriptase increase thermostability through tighter binding to template-primer

Nucleic Acids Res. 2009 Feb;37(2):473-81. doi: 10.1093/nar/gkn952. Epub 2008 Dec 4.

Abstract

In an effort to increase the thermostability of Moloney Murine Leukemia Virus reverse transcriptase (MMLV RT), we screened random and site-saturation libraries for variants that show increased resistance to thermal inactivation. We discovered five mutations E69K, E302R, W313F, L435G and N454K that collectively increase the half-life of MMLV RT at 55 degrees C from less than 5 min to approximately 30 min in the presence of template-primer. In addition, these mutations alter the thermal profile by increasing specific activity of the pentuple mutant (M5) over a broad range of cDNA synthesis temperatures (25-70 degrees C). We further show that M5 generates higher cDNA yields and exhibits better RT-PCR performance compared to wild-type RT when used at high temperature to amplify RNA targets containing secondary structure. Finally, we demonstrate that M5 exhibits tighter binding (lower K(m)) to template-primer, which likely protects against heat inactivation.

MeSH terms

  • DNA Primers
  • DNA, Complementary / biosynthesis
  • Hot Temperature*
  • Humans
  • Moloney murine leukemia virus / enzymology*
  • Mutagenesis
  • Point Mutation*
  • Protein Binding
  • Protein Stability
  • RNA-Directed DNA Polymerase / chemistry
  • RNA-Directed DNA Polymerase / genetics*
  • RNA-Directed DNA Polymerase / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Templates, Genetic

Substances

  • DNA Primers
  • DNA, Complementary
  • RNA-Directed DNA Polymerase