Literature DB >> 30097871

HPLC-Based Enzyme Assays for Sirtuins.

Jun Young Hong1, Xiaoyu Zhang1, Hening Lin2,3.   

Abstract

Sirtuins are a class of enzymes that utilize nicotinamide adenine dinucleotide, NAD+, to remove various acyl groups from protein lysine residues. They have important biological functions and regulate numerous biological pathways. Small molecules that can modulate sirtuin enzymatic activities are potential therapeutic candidates to treat various human diseases. This protocol describes a high-performance liquid chromatography (HPLC)-based method to measure the enzyme kinetics for SIRT2 and SIRT6's demyristoylase activities and SIRT5's desuccinylase activity. This method uses peptide substrates that resemble physiological substrates and thus can give more reliable kinetic parameters (K m and k cat values) for these enzymes. The data obtained are useful for understanding the biological function of sirtuins and developing sirtuin modulators.

Entities:  

Keywords:  Demyristoylase; Desuccinylase; Enzymatic activity assay; High-performance liquid chromatography assay; SIRT2; SIRT5; SIRT6

Mesh:

Substances:

Year:  2018        PMID: 30097871      PMCID: PMC6893877          DOI: 10.1007/978-1-4939-8588-3_15

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  9 in total

Review 1.  The biochemistry of sirtuins.

Authors:  Anthony A Sauve; Cynthia Wolberger; Vern L Schramm; Jef D Boeke
Journal:  Annu Rev Biochem       Date:  2006       Impact factor: 23.643

Review 2.  Ten years of NAD-dependent SIR2 family deacetylases: implications for metabolic diseases.

Authors:  Shin-ichiro Imai; Leonard Guarente
Journal:  Trends Pharmacol Sci       Date:  2010-03-11       Impact factor: 14.819

3.  Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase.

Authors:  S Imai; C M Armstrong; M Kaeberlein; L Guarente
Journal:  Nature       Date:  2000-02-17       Impact factor: 49.962

Review 4.  The multifaceted functions of sirtuins in cancer.

Authors:  Angeliki Chalkiadaki; Leonard Guarente
Journal:  Nat Rev Cancer       Date:  2015-09-18       Impact factor: 60.716

5.  A SIRT2-Selective Inhibitor Promotes c-Myc Oncoprotein Degradation and Exhibits Broad Anticancer Activity.

Authors:  Hui Jing; Jing Hu; Bin He; Yashira L Negrón Abril; Jack Stupinski; Keren Weiser; Marisa Carbonaro; Ying-Ling Chiang; Teresa Southard; Paraskevi Giannakakou; Robert S Weiss; Hening Lin
Journal:  Cancer Cell       Date:  2016-03-14       Impact factor: 31.743

6.  Sirt5 is a NAD-dependent protein lysine demalonylase and desuccinylase.

Authors:  Jintang Du; Yeyun Zhou; Xiaoyang Su; Jiu Jiu Yu; Saba Khan; Hong Jiang; Jungwoo Kim; Jimin Woo; Jun Huyn Kim; Brian Hyun Choi; Bin He; Wei Chen; Sheng Zhang; Richard A Cerione; Johan Auwerx; Quan Hao; Hening Lin
Journal:  Science       Date:  2011-11-11       Impact factor: 47.728

Review 7.  Sirtuins in epigenetic regulation.

Authors:  Hui Jing; Hening Lin
Journal:  Chem Rev       Date:  2015-01-28       Impact factor: 60.622

8.  Efficient demyristoylase activity of SIRT2 revealed by kinetic and structural studies.

Authors:  Yan-Bin Teng; Hui Jing; Pornpun Aramsangtienchai; Bin He; Saba Khan; Jing Hu; Hening Lin; Quan Hao
Journal:  Sci Rep       Date:  2015-02-23       Impact factor: 4.379

9.  Identifying the functional contribution of the defatty-acylase activity of SIRT6.

Authors:  Xiaoyu Zhang; Saba Khan; Hong Jiang; Marc A Antonyak; Xiao Chen; Nicole A Spiegelman; Jonathan H Shrimp; Richard A Cerione; Hening Lin
Journal:  Nat Chem Biol       Date:  2016-06-20       Impact factor: 15.040

  9 in total
  1 in total

1.  Cyclic Peptide-Based Sirtuin Substrates.

Authors:  Di Chen; Lingling Yan; Weiping Zheng
Journal:  Molecules       Date:  2019-01-24       Impact factor: 4.411

  1 in total

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