Literature DB >> 8970171

A method for introducing site-specific mutations using oligonucleotide primers and its application to site-saturation mutagenesis.

M J O'Donohue1, G G Kneale.   

Abstract

Oligonucleotide primer-directed mutagenesis is a useful molecular biological tool, which is invaluable for the study of the structure/function relationships in proteins and for the creation of mutant proteins possessing modified or novel biological activities. Mutagenesis studies in which a site-saturation approach is employed require a high-efficiency mutagenesis procedure, which will generate a population of mutated molecules containing an even distribution of all possible amino acid changes, or a subset thereof. This article describes such a mutagenesis technique and discusses the adaptations that are necessary to perform site-saturation mutagenesis.

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Year:  1996        PMID: 8970171     DOI: 10.1007/bf02740772

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  20 in total

1.  A simple and efficient method for the oligodeoxyribonucleotide-directed mutagenesis of double-stranded plasmid DNA.

Authors:  R Jung; M P Scott; L O Oliveira; N C Nielsen
Journal:  Gene       Date:  1992-11-02       Impact factor: 3.688

2.  A general and fast method to generate multiple site directed mutations.

Authors:  I Mikaelian; A Sergeant
Journal:  Nucleic Acids Res       Date:  1992-01-25       Impact factor: 16.971

Review 3.  Plasmid transformation of Escherichia coli and other bacteria.

Authors:  D Hanahan; J Jessee; F R Bloom
Journal:  Methods Enzymol       Date:  1991       Impact factor: 1.600

4.  The rapid generation of oligonucleotide-directed mutations at high frequency using phosphorothioate-modified DNA.

Authors:  J W Taylor; J Ott; F Eckstein
Journal:  Nucleic Acids Res       Date:  1985-12-20       Impact factor: 16.971

5.  Inhibition of restriction endonuclease Nci I cleavage by phosphorothioate groups and its application to oligonucleotide-directed mutagenesis.

Authors:  K L Nakamaye; F Eckstein
Journal:  Nucleic Acids Res       Date:  1986-12-22       Impact factor: 16.971

6.  Replacements of Pro86 in phage T4 lysozyme extend an alpha-helix but do not alter protein stability.

Authors:  T Alber; J A Bell; D P Sun; H Nicholson; J A Wozniak; S Cook; B W Matthews
Journal:  Science       Date:  1988-02-05       Impact factor: 47.728

7.  Efficient saturation mutagenesis of a pentapeptide coding sequence using mixed oligonucleotides.

Authors:  S A Goff; S R Short-Russell; J F Dice
Journal:  DNA       Date:  1987-08

8.  5'-3' exonucleases in phosphorothioate-based oligonucleotide-directed mutagenesis.

Authors:  J R Sayers; W Schmidt; F Eckstein
Journal:  Nucleic Acids Res       Date:  1988-02-11       Impact factor: 16.971

9.  Improved method for PCR-mediated site-directed mutagenesis.

Authors:  D Barettino; M Feigenbutz; R Valcárcel; H G Stunnenberg
Journal:  Nucleic Acids Res       Date:  1994-02-11       Impact factor: 16.971

10.  Rapid and efficient site-specific mutagenesis without phenotypic selection.

Authors:  T A Kunkel
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

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