Potent and Specific Activators for Mitochondrial Sirtuins Sirt3 and Sirt5

被引:26
作者
Suenkel, Benjamin [1 ]
Valente, Sergio [2 ,3 ]
Zwergel, Clemens [2 ,3 ]
Weiss, Sandra [1 ]
Di Bello, Elisabetta [2 ,3 ]
Fioravanti, Rossella [2 ,3 ]
Aventaggiato, Michele [4 ]
Amorim, Joao A. [5 ,6 ,7 ]
Garg, Neha [7 ]
Kumar, Surinder [8 ]
Lombard, David B. [8 ,9 ]
Hu, Tuo [10 ]
Singh, Pankaj K. [10 ,11 ]
Tafani, Marco [4 ,12 ]
Palmeira, Carlos M. [5 ,6 ]
Sinclair, David [7 ]
Mai, Antonello [2 ,3 ]
Steegborn, Clemens [1 ]
机构
[1] Univ Bayreuth, Dept Biochem, D-95440 Bayreuth, Germany
[2] Sapienza Univ Rome, Dept Drug Chem & Technol, I-00185 Rome, Italy
[3] Pasteur Inst, Cenci Bolognetti Fdn, I-00185 Rome, Italy
[4] Sapienza Univ Rome, Dept Expt Med, I-00161 Rome, Italy
[5] Univ Coimbra, Dept Life Sci, Coimbra, Portugal
[6] Univ Coimbra, Ctr Neurosci & Cell Biol, P-3004504 Coimbra, Portugal
[7] Harvard Med Sch, Blavatnik Inst, Glenn Ctr Biol Aging Res, Genet Dept, Boston, MA 02115 USA
[8] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
[9] Univ Michigan, Inst Gerontol, Ann Arbor, MI 48109 USA
[10] Univ Nebraska Med Ctr, Eppley Inst Res Canc & Allied Dis, Omaha, NE 68198 USA
[11] Univ Nebraska Med Ctr, Dept Biochem & Mol Biol, Omaha, NE 68198 USA
[12] Univ Nebraska Med Ctr, Dept Pathol & Microbiol, Omaha, NE 68198 USA
关键词
SMALL-MOLECULE ACTIVATORS; 1,4-DIHYDROPYRIDINES; INHIBITION; TARGETS; RESVERATROL; COMPLEXES; MECHANISM; DISCOVERY; DESIGN;
D O I
10.1021/acs.jmedchem.2c01215
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Sirtuins are NAD+-dependent protein deacylases involved in metabolic regulation and aging-related diseases. Specific activators for seven human Sirtuin isoforms would be important chemical tools and potential therapeutic drugs. Activators have been described for Sirt1 and act via a unique N-terminal domain of this isoform. For most other Sirtuin isoforms, including mitochondrial Sirt3-5, no potent and specific activators have yet been identified. We here describe the identification and character-ization of 1,4-dihydropyridine-based compounds that either act as pan Sirtuin activators or specifically stimulate Sirt3 or Sirt5. The activators bind to the Sirtuin catalytic cores independent of NAD+ and acylated peptides and stimulate turnover of peptide and protein substrates. The compounds also activate Sirt3 or Sirt5 in cellular systems regulating, e.g., apoptosis and electron transport chain. Our results provide a scaffold for potent Sirtuin activation and derivatives specific for Sirt3 and Sirt5 as an excellent basis for further drug development.
引用
收藏
页码:14015 / 14031
页数:17
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