Marinopyrrole A Target Elucidation by Acyl Dye Transfer

被引:95
作者
Hughes, Chambers C. [4 ]
Yang, Yu-Liang [1 ,2 ,3 ]
Liu, Wei-Ting [1 ,2 ,3 ]
Dorrestein, Pieter C. [1 ,2 ,3 ]
La Clair, James J. [5 ]
Fenical, William [4 ]
机构
[1] Univ Calif San Diego, Dept Chem, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Biochem, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Scripps Inst Oceanog, Ctr Marine Biotechnol & Biomed, La Jolla, CA 92093 USA
[5] Xenobe Res Inst, San Diego, CA 92164 USA
关键词
NATURAL-PRODUCTS; OLEFIN METATHESIS; CHEMICAL BIOLOGY; CLICK CHEMISTRY; REAGENTS; STRATEGIES; PROTEINS; PEPTIDES;
D O I
10.1021/ja903149u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The targeting of marinopyrrole A to actin was identified using a fluorescent dye transfer strategy. The process began by appending a carboxylic acid terminal tag to a phenol in the natural product. The resulting probe was then studied in live cells to verify that it maintained activity comparable to marinopyrrole A. Two-color fluorescence microscopy confirmed that both unlabeled and labeled materials share comparable uptake and subcellular Localization in HCT-116 cells. Subsequent immunoprecipitation studies identified actin as a putative target in HCT-116 cells, a result that was validated by mass spectral, affinity, and activity analyses on purified samples of actin. Further data analyses indicated that the dye in the marinopyrrole probe was selectively transferred to a single residue K,15, an event that did not occur with related acyl phenols and reactive labels. In this study, the combination of cell, protein, and amino acid analysis arose from a single sample of material, thereby, suggesting a means to streamline and reduce material requirements involved in mode of action studies.
引用
收藏
页码:12094 / +
页数:5
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