Kilic Funda, Kashikar Nachiket D, Schmidt Reinhard, Alvarez Luis, Dai Luru, Weyand Ingo, Wiesner Burkhard, Goodwin Normann, Hagen Volker, Kaupp U Benjamin
Leibniz-Institut für Molekulare Pharmakologie, Berlin, Germany.
J Am Chem Soc. 2009 Mar 25;131(11):4027-30. doi: 10.1021/ja808334f.
Ketalization of the biomolecule progesterone with (6-bromo-7-hydroxycoumarin-4-yl)ethane-1,2-diol gives the photolabile progesterone derivatives 3 and 4. These compounds display dramatically reduced bioactivity and release progesterone upon irradiation with UV/vis or IR light. In particular, 4 can be used to perform concentration-jump experiments with high temporal and spatial resolution that allows one to study elegantly the mechanisms of rapid nongenomic cellular events evoked by progesterone. The usefulness of 4 was demonstrated by measurement of changes in swimming behavior of single human sperm caused by progesterone-induced Ca(2+) influx in the sperm flagellum.
生物分子孕酮与(6-溴-7-羟基香豆素-4-基)乙烷-1,2-二醇进行缩酮化反应,得到光不稳定的孕酮衍生物3和4。这些化合物的生物活性显著降低,并在紫外/可见或红外光照射下释放孕酮。特别是,化合物4可用于进行具有高时间和空间分辨率的浓度跃变实验,从而能够巧妙地研究孕酮引发的快速非基因组细胞事件的机制。通过测量孕酮诱导精子鞭毛中Ca(2+)内流导致的单个人类精子游泳行为变化,证明了化合物4的实用性。