Ultrafast anisotropic decay is a prominent parameter revealing ultrafast energy and electron transfer; however, it is dimcult to be determined reliably owing to the requirement of a simultaneous availability of the pa...Ultrafast anisotropic decay is a prominent parameter revealing ultrafast energy and electron transfer; however, it is dimcult to be determined reliably owing to the requirement of a simultaneous availability of the parallel and perpendieular polarized decay kinetics. Nowadays, any measurement of anisotropic decay is a kind of approach to the exact simultaneity. Here we report a novel method for a synchronous ultrafast anisotropy decay measurement, which can well determine the anisotropy, even at a very early time, as the rising phase of the excitation laser pulse. The anisotropic decay of the B850 in bacteriM light harvesting antenna complex LH2 of rhodobacter sphaeroides in solution at room temperature with coherent excitation is detected by this method, which shows a polarization response time of 30 fs, and the energy transfer from the initial excitation to the bacteriochlorophylls in B850 ring takes about 7Ors. The anisotropic decay that is probed at the red side of the absorption spectrum, such as 880 nm, has an initial value of 0.4, corresponding to simulated emission, while the blue side with an anisotropy of 0.1 contributes to the ground-state bleaching. Our results show that the coherent excitation covering the whole ring might not be realized owing to the symmetry breaking of LH2： from C9 symmetry in membrane to C2 symmetry in solution.展开更多
Structures of membrane protein in solution are different from that in crystal phase. We present the primary results of small angle x-ray scattering （SAXS） resolved topological structures of a light harvesting antenn...Structures of membrane protein in solution are different from that in crystal phase. We present the primary results of small angle x-ray scattering （SAXS） resolved topological structures of a light harvesting antenna membrane protein complex LH2 from photosynthetic bacteria Rhodopseudomonas acidophila in detergent solution for the first time. Our results show that the elliptical shape of the LH2 complex in solution clearly deviates from its circular structure in crystal phase determined by x-ray diffraction. This result provides an insight into the structure and function interplay in LH2.展开更多
基金Supported by the National Natural Science Foundation of China under Grant Nos 20925313,21227003,and 11004236the National Basic Research Program of China under Grant No 2009CB930700the Innovation Program of Chinese Academy of Sciences under Grant No KJCX2-YW-W25
文摘Ultrafast anisotropic decay is a prominent parameter revealing ultrafast energy and electron transfer; however, it is dimcult to be determined reliably owing to the requirement of a simultaneous availability of the parallel and perpendieular polarized decay kinetics. Nowadays, any measurement of anisotropic decay is a kind of approach to the exact simultaneity. Here we report a novel method for a synchronous ultrafast anisotropy decay measurement, which can well determine the anisotropy, even at a very early time, as the rising phase of the excitation laser pulse. The anisotropic decay of the B850 in bacteriM light harvesting antenna complex LH2 of rhodobacter sphaeroides in solution at room temperature with coherent excitation is detected by this method, which shows a polarization response time of 30 fs, and the energy transfer from the initial excitation to the bacteriochlorophylls in B850 ring takes about 7Ors. The anisotropic decay that is probed at the red side of the absorption spectrum, such as 880 nm, has an initial value of 0.4, corresponding to simulated emission, while the blue side with an anisotropy of 0.1 contributes to the ground-state bleaching. Our results show that the coherent excitation covering the whole ring might not be realized owing to the symmetry breaking of LH2： from C9 symmetry in membrane to C2 symmetry in solution.
基金Supported by the National Natural Science Foundation of China under Grant Nos 10375075, 60321003, and 60438020, the National Key Basic Research and Development Programme of China under Grant No G1998010102, and the Knowledge Innovation Project of Chinese Academy of Sciences under Grant No KJCX2-SW-W14.
文摘Structures of membrane protein in solution are different from that in crystal phase. We present the primary results of small angle x-ray scattering （SAXS） resolved topological structures of a light harvesting antenna membrane protein complex LH2 from photosynthetic bacteria Rhodopseudomonas acidophila in detergent solution for the first time. Our results show that the elliptical shape of the LH2 complex in solution clearly deviates from its circular structure in crystal phase determined by x-ray diffraction. This result provides an insight into the structure and function interplay in LH2.
