Time-resolved electron paramagnetic resonance study of photoionization of tyrosine anion in aqueous solution

被引:14
作者
Clancy, CMR [1 ]
Forbes, MDE [1 ]
机构
[1] Univ N Carolina, Dept Chem, Venable & Kenan Labs, Chapel Hill, NC 27599 USA
关键词
D O I
10.1111/j.1751-1097.1999.tb05300.x
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
Photoionization of the amino acid tyrosine in basic water was studied by time-resolved electron paramagnetic resonance (TREPR) at X-band (9.5 GHz), Photoionization of deprotonated tyrosine leads to a spin-polarized emissive/absorptive chemically induced dynamic electron polarization (CIDEP) spectrum produced by the radical pair mechanism, with the tyrosyl radical in emission and the solvated electron in absorption, which implies a triplet precursor. The exchange interaction, J, is found to be negative for this radical pair. The triplet photoionization channel is determined to be monophotonic. The singlet channel of photoionization of deprotonated tyrosine is seen only upon addition of the electron acceptor 2-bromo-2-methylpropionic acid (BMPA) to the sample. The singlet channel is isolated by performing TREPR on a sample containing tyrosine, BMPA and a triplet quencher (2,4-hexadienoic acid). This channel is also found to be monophotonic.
引用
收藏
页码:16 / 21
页数:6
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