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用于从复杂蛋白质组中综合检测和鉴定酶活性的三功能化学探针。

Trifunctional chemical probes for the consolidated detection and identification of enzyme activities from complex proteomes.

作者信息

Adam Gregory C, Sorensen Erik J, Cravatt Benjamin F

机构信息

The Skaggs Institute for Chemical Biology and the Department of Chemistry, The Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

Mol Cell Proteomics. 2002 Oct;1(10):828-35. doi: 10.1074/mcp.t200007-mcp200.

Abstract

Chemical probes that covalently modify the active sites of enzymes in complex proteomes are useful tools for identifying enzyme activities associated with discrete (patho) physiological states. Researchers in proteomics typically use two types of activity-based probes to fulfill complementary objectives: fluorescent probes for rapid and sensitive target detection and biotinylated probes for target purification and identification. Accordingly we hypothesized that a strategy in which the target detection and target isolation steps of activity-based proteomic experiments were merged might accelerate the characterization of differentially expressed protein activities. Here we report the synthesis and application of trifunctional chemical proteomic probes in which elements for both target detection (e.g. rhodamine) and isolation (e.g. biotin) are appended to a sulfonate ester reactive group, permitting the consolidated visualization and affinity purification of labeled proteins by a combination of in-gel fluorescence and avidin chromatography procedures. A trifunctional phenyl sulfonate probe was used to identify several technically challenging protein targets, including the integral membrane enzyme 3beta-hydroxysteroid dehydrogenase/Delta5-isomerase and the cofactor-dependent enzymes platelet-type phosphofructokinase and type II tissue transglutaminase. The latter two enzyme activities were significantly up-regulated in the invasive estrogen receptor-negative (ER(-)) human breast cancer cell line MDA-MB-231 relative to the non-invasive ER(+) breast cancer lines MCF7 and T-47D. Collectively these studies demonstrate that chemical proteomic probes incorporating elements for both target detection and target isolation fortify the important link between the visualization of differentially expressed enzyme activities and their subsequent molecular identification, thereby augmenting the information content achieved in activity-based profiling experiments.

摘要

能够共价修饰复杂蛋白质组中酶活性位点的化学探针,是用于鉴定与离散(病理)生理状态相关的酶活性的有用工具。蛋白质组学研究人员通常使用两种基于活性的探针来实现互补目标:用于快速灵敏地检测靶标的荧光探针,以及用于靶标纯化和鉴定的生物素化探针。因此,我们推测,将基于活性的蛋白质组学实验中的靶标检测和靶标分离步骤合并的策略,可能会加速差异表达蛋白质活性的表征。在此,我们报告了三功能化学蛋白质组学探针的合成与应用,其中用于靶标检测(如罗丹明)和分离(如生物素)的元素连接到磺酸酯反应基团上,通过凝胶内荧光和抗生物素蛋白色谱法的组合,允许对标记蛋白质进行整合可视化和亲和纯化。一种三功能苯磺酸盐探针被用于鉴定几个技术上具有挑战性的蛋白质靶标,包括膜整合酶3β-羟基类固醇脱氢酶/Δ5-异构酶以及辅因子依赖性酶血小板型磷酸果糖激酶和II型组织转谷氨酰胺酶。相对于非侵袭性雌激素受体阳性(ER(+))乳腺癌细胞系MCF7和T-47D,后两种酶活性在侵袭性雌激素受体阴性(ER(-))人乳腺癌细胞系MDA-MB-231中显著上调。这些研究共同表明,结合了靶标检测和靶标分离元素的化学蛋白质组学探针加强了差异表达酶活性可视化与其后续分子鉴定之间的重要联系,从而增加了基于活性的分析实验所获得的信息内容。

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