Photochemical selectivity in guanine-cytosine base-pair structures

被引:203
作者
Abo-Riziq, A
Grace, L
Nir, E
Kabelac, M
Hobza, P
de Vries, MS [1 ]
机构
[1] Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[2] Acad Sci Czech Republ, Inst Organ Chem & Biochem, Prague 16610 6, Czech Republic
关键词
ab initio computation; DNA base pairs; IR-UV spectroscopy; jet cooling; photochemistry;
D O I
10.1073/pnas.0408574102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Prebiotic chemistry presumably took place before formation of an oxygen-rich atmosphere and thus under conditions of intense short wavelength UV irradiation. Therefore, the UV photochemical stability of the molecular building blocks of life may have been an important selective factor in determining the eventual chemical makeup of critical biomolecules. To investigate the role of UV irradiation in base-pairing we have studied guanine (G) and cytosine (C) base pairs in the absence of the RNA backbone. We distinguished base-pair structures by IR-UV hole-burning spectroscopy as well as by high-level correlated ab initio calculations. The Watson-Crick structure exhibits broad UV absorption, in stark contrast to other GC structures and other base-pair structures. This broad absorption may be explained by a rapid internal conversion that makes this specific base pair arrangement uniquely photochemically stable.
引用
收藏
页码:20 / 23
页数:4
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