Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany.
J Biol Chem. 2010 May 7;285(19):14603-9. doi: 10.1074/jbc.M109.086314. Epub 2010 Mar 16.
Reversibly switchable fluorescent proteins can be repeatedly photoswitched between a fluorescent and a nonfluorescent state by irradiation with the light of two different wavelengths. The molecular basis of the switching process remains a controversial topic. Padron0.9 is a reversibly switchable fluorescent protein with "positive" switching characteristics, exhibiting excellent spectroscopic properties. Its chromophore is formed by the amino acids Cys-Tyr-Gly. We obtained high resolution x-ray structures of Padron0.9 in both the fluorescent and the nonfluorescent states and used the structural information for molecular dynamics simulations. We found that in Padron0.9 the chromophore undergoes a cis-trans isomerization upon photoswitching. The molecular dynamics simulations clarified the protonation states of the amino acid residues within the chromophore pocket that influence the protonation state of the chromophore. We conclude that a light driven cis-trans isomerization of the chromophore appears to be the fundamental switching mechanism in all photochromic fluorescent proteins known to date. Distinct absorption cross-sections for the switching wavelengths in the fluorescent and the nonfluorescent state are not essential for efficient photochromism in fluorescent proteins, although they may facilitate the switching process.
可反复切换的荧光蛋白可以通过两种不同波长的光照射在荧光和非荧光状态之间反复切换。切换过程的分子基础仍然是一个有争议的话题。Padron0.9 是一种具有“正”切换特性的可反复切换的荧光蛋白,具有优异的光谱特性。其发色团由半胱氨酸-酪氨酸-甘氨酸氨基酸组成。我们获得了 Padron0.9 在荧光和非荧光状态下的高分辨率 X 射线结构,并利用结构信息进行了分子动力学模拟。我们发现,在 Padron0.9 中,发色团在光开关时经历顺反异构化。分子动力学模拟澄清了影响发色团质子化状态的发色团口袋内氨基酸残基的质子化状态。我们的结论是,在迄今为止已知的所有光致变色荧光蛋白中,发色团的光驱动顺反异构似乎是基本的开关机制。在荧光和非荧光状态下的切换波长的不同吸收截面对于荧光蛋白的高效光致变色并非必需,尽管它们可能有助于切换过程。