Courtney Taylor M, Hankinson Chasity P, Horst Trevor J, Deiters Alexander
Department of Chemistry, University of Pittsburgh Pittsburgh PA 15260 USA
Chem Sci. 2021 Sep 22;12(40):13425-13433. doi: 10.1039/d1sc04464h. eCollection 2021 Oct 20.
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.
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。