共 22 条
Global Profiling of Acetyltransferase Feedback Regulation
被引:39
作者:

Montgomery, David C.
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NCI, Biol Chem Lab, Frederick, MD 21702 USA NCI, Biol Chem Lab, Frederick, MD 21702 USA

Garlick, Julie M.
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机构:
NCI, Biol Chem Lab, Frederick, MD 21702 USA NCI, Biol Chem Lab, Frederick, MD 21702 USA

Kulkarni, Rhushikesh A.
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机构:
NCI, Biol Chem Lab, Frederick, MD 21702 USA NCI, Biol Chem Lab, Frederick, MD 21702 USA

Kennedy, Steven
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机构:
Univ Toronto, Struct Genom Consortium, Toronto, ON MG5 1L7, Canada NCI, Biol Chem Lab, Frederick, MD 21702 USA

Allali-Hassani, Abdellah
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机构:
Univ Toronto, Struct Genom Consortium, Toronto, ON MG5 1L7, Canada NCI, Biol Chem Lab, Frederick, MD 21702 USA

Kuo, Yin-Ming
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机构:
Fox Chase Canc Ctr, Philadelphia, PA 19111 USA NCI, Biol Chem Lab, Frederick, MD 21702 USA

Andrews, Andrew J.
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h-index: 0
机构:
Fox Chase Canc Ctr, Philadelphia, PA 19111 USA NCI, Biol Chem Lab, Frederick, MD 21702 USA

Wu, Hong
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h-index: 0
机构:
Univ Toronto, Struct Genom Consortium, Toronto, ON MG5 1L7, Canada NCI, Biol Chem Lab, Frederick, MD 21702 USA

Vedadi, Masoud
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h-index: 0
机构:
Univ Toronto, Struct Genom Consortium, Toronto, ON MG5 1L7, Canada NCI, Biol Chem Lab, Frederick, MD 21702 USA

Meier, Jordan L.
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h-index: 0
机构:
NCI, Biol Chem Lab, Frederick, MD 21702 USA
Univ Toronto, Dept Pharmacol & Toxicol, 100 Coll St, Toronto, ON M5S 1A8, Canada NCI, Biol Chem Lab, Frederick, MD 21702 USA
机构:
[1] NCI, Biol Chem Lab, Frederick, MD 21702 USA
[2] Univ Toronto, Struct Genom Consortium, Toronto, ON MG5 1L7, Canada
[3] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[4] Univ Toronto, Dept Pharmacol & Toxicol, 100 Coll St, Toronto, ON M5S 1A8, Canada
基金:
巴西圣保罗研究基金会;
英国惠康基金;
加拿大创新基金会;
关键词:
HISTONE ACETYLTRANSFERASES;
LYSINE ACETYLTRANSFERASES;
METABOLIC-REGULATION;
ACETYLATION;
CELL;
P300;
INHIBITION;
COFACTORS;
MECHANISM;
BINDING;
D O I:
10.1021/jacs.6b03036
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Lysine acetyltransferases (KATs) are key mediators of cell signaling. Methods capable of providing new insights into their regulation thus constitute an important goal. Here we report an optimized platform for profiling KAT ligand interactions in complex proteomes using inhibitor-functionalized capture resins. This approach greatly expands the scope of KATs, KAT complexes, and CoA-dependent enzymes accessible to chemoproteomic methods. This enhanced profiling platform is then applied in the most comprehensive analysis to date of KAT inhibition by the feedback metabolite CoA. Our studies reveal that members of the KAT superfamily possess a spectrum of sensitivity to CoA and highlight NAT10 as a novel KAT that may be susceptible to metabolic feedback inhibition. This platform provides a powerful tool to define the potency and selectivity of reversible stimuli, such as small molecules and metabolites, that regulate KAT-dependent signaling.
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收藏
页码:6388 / 6391
页数:4
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