Müller Marc G, Lindner Ingo, Martin Iris, Gärtner Wolfgang, Holzwarth Alfred R
Max-Planck-Institut für Bioanorganische Chemie, D-45470 Mülheim a.d. Ruhr, Germany.
Biophys J. 2008 Jun;94(11):4370-82. doi: 10.1529/biophysj.106.091652. Epub 2008 Jan 16.
The photoprocesses of native (phyA of oat), and of C-terminally truncated recombinant phytochromes, assembled instead of the native phytochromobilin with phycocyanobilin (PCB-65 kDa-phy) and iso-phycocyanobilin (iso-PCB-65 kDa-phy) chromophores, have been studied by femtosecond transient absorption spectroscopy in both their red absorbing phytochrome (P(r)) and far-red absorbing phytochrome (P(fr)) forms. Native P(r) phytochrome shows an excitation wavelength dependence of the kinetics with three main picosecond components. The formation kinetics of the first ground-state intermediate I(700), absorbing at approximately 690 nm, is mainly described by 28 ps or 40 ps components in native and PCB phytochrome, respectively, whereas additional approximately 15 and 50 ps components describe conformational dynamics and equilibria among different local minima on the excited-state hypersurface. No significant amount of I(700) formation can be observed on our timescale for iso-PCB phytochrome. We suggest that iso-PCB-65 kDa-phy either interacts with the protein differently leading to a more twisted and/or less protonated configuration, or undergoes P(r) to P(fr) isomerization primarily via a different configurational pathway, largely circumventing I(700) as an intermediate. The isomerization process is accompanied by strong coherent oscillations due to wavepacket motion on the excited-state surface for both phytochrome forms. The femto- to (sub-)nanosecond kinetics of the P(fr) forms is again quite similar for the native and the PCB phytochromes. After an ultrafast excited-state relaxation within approximately 150 fs, the chromophores return to the first ground-state intermediate in 400-800 fs followed by two additional ground-state intermediates which are formed with 2-3 ps and approximately 400 ps lifetimes. We call the first ground-state intermediate in native phytochrome I(fr 750), due to its pronounced absorption at that wavelength. The other intermediates are termed I(fr 675) and pseudo-P(r). The absorption spectrum of the latter already closely resembles the absorption of the P(r) chromophore. PCB-65 kDa-phy shows a very similar kinetics, although many of the detailed spectral features in the transients seen in native phy are blurred, presumably due to wider inhomogeneous distribution of the chromophore conformation. Iso-PCB-65 kDa-phy shows similar features to the PCB-65 kDa-phy, with some additional blue-shift of the transient spectra of approximately 10 nm. The sub-200 fs component is, however, absent, and the picosecond lifetimes are somewhat longer than in 124 kDa phytochrome or in PCB-65 kDa-phy. We interpret the data within the framework of two- and three-dimensional potential energy surface diagrams for the photoisomerization processes and the ground-state intermediates involved in the two photoconversions.
利用飞秒瞬态吸收光谱,研究了天然(燕麦的phyA)以及C端截短的重组光敏色素的光过程。这些重组光敏色素分别与藻蓝胆素(PCB-65 kDa-phy)和异藻蓝胆素(iso-PCB-65 kDa-phy)发色团组装,替代了天然的藻胆素。研究了它们处于红光吸收型光敏色素(P(r))和远红光吸收型光敏色素(P(fr))两种形式下的情况。天然P(r)光敏色素的动力学表现出激发波长依赖性,具有三个主要的皮秒成分。第一个基态中间体I(700)(在约690 nm处有吸收)的形成动力学,在天然和PCB光敏色素中分别主要由28 ps或40 ps的成分描述,而另外约15 ps和50 ps的成分描述了激发态超曲面上不同局部极小值之间的构象动力学和平衡。在我们的时间尺度上,未观察到iso-PCB光敏色素有大量I(700)形成。我们认为,iso-PCB-65 kDa-phy要么与蛋白质的相互作用不同,导致更扭曲和/或质子化程度更低的构型,要么主要通过不同的构型途径进行P(r)到P(fr)的异构化,很大程度上绕过I(700)作为中间体。异构化过程伴随着由于激发态表面上的波包运动而产生的强烈相干振荡,两种光敏色素形式均如此。P(fr)形式的飞秒到(亚)纳秒动力学,对于天然和PCB光敏色素来说再次非常相似。在约150 fs内超快的激发态弛豫之后,发色团在400 - 800 fs内回到第一个基态中间体,随后是另外两个基态中间体,它们的形成寿命分别为2 - 3 ps和约400 ps。由于其在该波长处有明显吸收,我们将天然光敏色素中的第一个基态中间体称为I(fr 750)。其他中间体称为I(fr 675)和假P(r)。后者的吸收光谱已经与P(r)发色团的吸收非常相似。PCB-65 kDa-phy表现出非常相似的动力学,尽管在天然phy中观察到的瞬态中的许多详细光谱特征变得模糊,可能是由于发色团构象的不均匀分布更宽。Iso-PCB-65 kDa-phy表现出与PCB-65 kDa-phy相似的特征,瞬态光谱有大约10 nm的额外蓝移。然而,小于200 fs的成分不存在,皮秒寿命比1型24 kDa光敏色素或PCB-65 kDa-phy中的稍长。我们在二维和三维势能面图的框架内解释了光异构化过程以及两个光转换中涉及的基态中间体的数据。