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Analysis of Point Mutations by Use of Amber Stop Codon Suppression

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Part of the book series: Methods In Molecular Medicine™ ((MIMB,volume 57))

Abstract

It is often necessary to make multiple amino acid substitutions at a particular site to determine the function of the wild-type amino acid in protein structure and function studies. Each substitution requires a unique mutation at that site. An alternative to making a series of predetermined substitutions is to create a library of mutations at that site that encompasses all possible amino acid substitutions. The creation of such libraries is often simple. Screening the number of clones necessary to insure a complete representation of substitutions can be difficult and time consuming. Amino acid substitution by amber suppression provides an alternative to standard site-directed mutagenesis and library approaches (1).

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References

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© 1996 Humana Press Inc.

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Lesley, S.A. (1996). Analysis of Point Mutations by Use of Amber Stop Codon Suppression. In: Trower, M.K. (eds) In Vitro Mutagenesis Protocols. Methods In Molecular Medicine™, vol 57. Humana Press. https://doi.org/10.1385/0-89603-332-5:65

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  • DOI: https://doi.org/10.1385/0-89603-332-5:65

  • Publisher Name: Humana Press

  • Print ISBN: 978-0-89603-332-0

  • Online ISBN: 978-1-59259-544-0

  • eBook Packages: Springer Protocols

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