Generating mammalian sirtuin tools for protein-interaction analysis.

Methods Mol Biol

Sarah W. Stedman Nutrition and Metabolism Center, Duke University Medical Center, Durham, NC, USA.

Published: April 2014

AI Article Synopsis

  • Sirtuins are crucial enzymes linked to aging, cancer, and metabolism, functioning by removing acyl groups from proteins.
  • Identifying specific sirtuin target proteins is challenging due to the abundance of acetylated proteins, but recent findings show sirtuin substrates often physically associate with their regulators.
  • The text outlines a method for discovering sirtuin interactors through molecular cloning and immunochemistry techniques, which includes creating expression plasmids and using a database for data analysis.

Article Abstract

The sirtuins are a family of NAD(+)-dependent deacylases with important effects on aging, cancer, and metabolism. Sirtuins exert their biological effects by catalyzing deacetylation and/or deacylation reactions in which Acyl groups are removed from lysine residues of specific proteins. A current challenge is to identify specific sirtuin target proteins against the high background of acetylated proteins recently identified by proteomic surveys. New evidence indicates that bona fide sirtuin substrate proteins form stable physical associations with their sirtuin regulator. Therefore, identification of sirtuin interacting proteins could be a useful aid in focusing the search for substrates. Described here is a method for identifying sirtuin protein interactors. Employing basic techniques of molecular cloning and immunochemistry, the method describes the generation of mammalian sirtuin protein expression plasmids and their use to overexpress and immunoprecipitate sirtuins with their interacting partners. Also described is the use of the Database for Annotation, Visualization, and Integrated Discovery for interpreting the sirtuin protein-interaction data obtained.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819116PMC
http://dx.doi.org/10.1007/978-1-62703-637-5_5DOI Listing

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