Unveiling the excited state energy transfer pathways in peridinin-chlorophyll a-protein by ultrafast multi-pulse transient absorption spectroscopy

被引:22
作者
Redeckas, Kipras [1 ]
Voiciuk, Vladislava [1 ]
Zigmantas, Donatas [2 ]
Hiller, Roger G. [3 ]
Vengris, Mikas [1 ]
机构
[1] Vilnius Univ, Fac Phys, Dept Quantum Elect, Sauletekio Ay 10, LT-10223 Vilnius, Lithuania
[2] Lund Univ, Dept Chem Phys, POB 124, S-22100 Lund, Sweden
[3] Macquarie Univ, Dept Biol Sci, N Ryde, NSW 2109, Australia
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2017年 / 1858卷 / 04期
关键词
Peridinin-chlorophyll alpha-protein; Pump-probe; Pump-dump-probe; Intramolecular charge transfer; Excited state equilibrium; Excitation energy transfer;
D O I
10.1016/j.bbabio.2017.01.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Time-resolved multi-pulse methods were applied to investigate the excited state dynamics, the interstate couplings, and the excited state energy transfer pathways between the light-harvesting pigments in peridinin-chlorophyll a-protein (PCP). The utilized pump-dump-probe techniques are based on perturbation of the regular PCP energy transfer pathway. The PCP complexes were initially excited with an ultrashort pulse, resonant to the S-0 -> S-2 transition of the carotenoid peridinin. A portion of the peridinin-based emissive intramolecular charge transfer (ICT) state was then depopulated by applying an ultrashort NIR pulse that perturbed the interaction between S-1 and ICT states and the energy flow from the carotenoids to the chlorophylls. The presented data indicate that the peridinin S-1 and ICT states are spectrally distinct and coexist in an excited state equilibrium in the PCP complex. Moreover, numeric analysis of the experimental data asserts ICT -> Chl-a as the main energy transfer pathway in the photoexcited PCP systems. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:297 / 307
页数:11
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