Femtosecond spectroscopic observations of initial intermediates in the photocycle of the photoactive yellow protein from Ectothiorhodospira halophila

被引:90
作者
Devanathan, S
Pacheco, A
Ujj, L
Cusanovich, M
Tollin, G [1 ]
Lin, S
Woodbury, N
机构
[1] Univ Arizona, Dept Biochem, Tucson, AZ 85721 USA
[2] Univ Arizona, Dept Chem, Tucson, AZ 85721 USA
[3] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0006-3495(99)76952-3
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Femtosecond time-resolved absorbance measurements were used to probe the subpicosecond primary events of the photoactive yellow protein (PYP), a 14-kD soluble photoreceptor from Ectothiorhodospira halophila. Previous picosecond absorption studies from our laboratory have revealed the presence of two new early photochemical intermediates in the PYP photocycle, I-0, which appears in less than or equal to 3 ps, and I-0(double dagger), which is formed in 220 ps, as well as stimulated emission from the PYP excited state. In the present study, kinetic measurements at two excitation wavelengths (395 nm and 460 nm) on either side of the PYP absorption maximum (446 nm) were undertaken using 100-fs pump and probe pulses. Global analysis over a range of probe wavelengths yielded time constants of 1.9 ps for the photochemical formation of the I-0 intermediate via the PYP excited state, and 3.4 ps for the repopulation of the ground state from the excited state. In addition to these pathways, 395 nm excitation also initiated an alternative route for PYP excitation and photochemistry, presumably involving a different excited electronic state of the chromophore. No photochemical intermediates formed before I-0 were observed. Based on these data, a quantum yield of 0.5-0.6 for I-0 formation was determined. The structural and mechanistic aspects of these results are discussed.
引用
收藏
页码:1017 / 1023
页数:7
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