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使用发色团修饰的雷帕霉素类似物进行靶向蛋白质氧化

Targeted protein oxidation using a chromophore-modified rapamycin analog.

作者信息

Courtney Taylor M, Hankinson Chasity P, Horst Trevor J, Deiters Alexander

机构信息

Department of Chemistry, University of Pittsburgh Pittsburgh PA 15260 USA

出版信息

Chem Sci. 2021 Sep 22;12(40):13425-13433. doi: 10.1039/d1sc04464h. eCollection 2021 Oct 20.

Abstract

Chemically induced dimerization of FKBP and FRB using rapamycin and rapamycin analogs has been utilized in a variety of biological applications. Formation of the FKBP-rapamycin-FRB ternary complex is typically used to activate a biological process and this interaction has proven to be essentially irreversible. In many cases, it would be beneficial to also have temporal control over deactivating a biological process once it has been initiated. Thus, we developed the first reactive oxygen species-generating rapamycin analog toward this goal. The BODIPY-rapamycin analog is capable of dimerizing FKBP and FRB to form a ternary complex, and upon irradiation with 530 nm light, generates singlet oxygen to oxidize and inactivate proteins of interest fused to FKBP/FRB.

摘要

使用雷帕霉素及其类似物对FKBP和FRB进行化学诱导二聚化已被应用于多种生物学领域。FKBP-雷帕霉素-FRB三元复合物的形成通常用于激活生物过程,并且这种相互作用已被证明基本上是不可逆的。在许多情况下,一旦启动生物过程后,若能对其失活进行时间控制将是有益的。因此,我们朝着这个目标开发了首个产生活性氧的雷帕霉素类似物。BODIPY-雷帕霉素类似物能够使FKBP和FRB二聚化以形成三元复合物,并且在用530 nm光照射时,会产生活性单线态氧以氧化并使与FKBP/FRB融合的目标蛋白失活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e40/8528027/b7c2b7d41af5/d1sc04464h-f1.jpg

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