| Literature DB >> 31941277 |
Simin Cao1, Haoyang Li1, Yangyi Liu1, Mengjie Zhang1, Mengyu Wang1, Zhongneng Zhou1, Jinquan Chen1, Sanjun Zhang1, Jianhua Xu1, Jay R Knutson2.
Abstract
The ultrafast solvation dynamics of reduced nicotinamide adenine dinucleotide (NADH) free in solution has been investigated, using both a femtosecond upconversion spectrophotofluorometer and a picosecond time-correlated single-photon counting (TCSPC) apparatus. The familiar time constant of solvent relaxation originating in "bulk water" was found to be ∼1.4 ps, revealing ultrafast solvent reorientation upon excitation. We also found a slower spectral relaxation process with an apparent time of 27 ps, suggesting there could either be dissociable "biological water" hydration sites on the surface of NADH or internal dielectric rearrangements of the flexible solvated molecule on that timescale. In contrast, the femtosecond fluorescence anisotropy measurement revealed that rotational diffusion happened on two different timescales (3.6 ps (local) and 141 ps (tumbling)); thus, any dielectric rearrangement scenario for the 27 ps relaxation must occur without significant chromophore oscillator rotation. The coexistence of quasi-static self quenching (QSSQ) with the slower relaxation is also discussed.Entities:
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Year: 2020 PMID: 31941277 PMCID: PMC7477843 DOI: 10.1021/acs.jpcb.9b10656
Source DB: PubMed Journal: J Phys Chem B ISSN: 1520-5207 Impact factor: 2.991