Photoion mass spectrometry of adenine, thymine and uracil in the 6-22 eV photon energy range

被引:161
作者
Jochims, HW
Schwell, M
Baumgärtel, H
Leach, S
机构
[1] CNRS, UMR 8112, LERMA, Observat Paris Meudon, F-92195 Meudon, France
[2] Univ Berlin, Inst Phys & Theoret Chem, D-14195 Berlin, Germany
[3] Univ Paris 07, CNRS, UMR 7583, Lab Interuniv Syst Atmospheriques, F-94010 Creteil, France
关键词
D O I
10.1016/j.chemphys.2005.03.008
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Using synchrotron radiation as excitation source in the 6-22 eV photon energy region, a photoionization mass spectrometry study of three nucleic acid bases, adenine, thymine and uracil, revealed VUV-induced degradation pathways of these important biological molecules. The fragmentation patterns, ionization energies and ion appearance energies (AE) are reported, many for the first time, and are compared with results of electron impact and other studies. AE values enabled heats of formation of parent and some fragment ions to be revised or determined for the first time. Thermochernical data, coupled with the observed AEs, were also useful in clarifying dissociative photoionization pathways. The main neutral loss species are HCN for adenine, HNCO and CO for thymine and uracil, but many subsequent and other fragmentation pathways, including some not suggested previously, are observed and discussed. The hyperconjugation properties of the methyl group make CO loss easier in thymine than in uracil. The astrophysically important fragment ion HCNH+ is shown to be formed by several fragmentation pathways in all three nucleobases. The relative importance of competitive fragmentation processes was determined in some cases. Some astrophysical implications concerning the prospects for observation and survival of these nucleic acid bases in the interstellar medium and in meteorites are briefly discussed. (c) 2005 Elsevier B.V. All rights reserved.
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页码:263 / 282
页数:20
相关论文
共 99 条
[31]   Electron attachment to uracil:: Effective destruction at subexcitation energies -: art. no. 188104 [J].
Hanel, G ;
Gstir, B ;
Denifl, S ;
Scheier, P ;
Probst, M ;
Farizon, B ;
Farizon, M ;
Illenberger, E ;
Märk, TD .
PHYSICAL REVIEW LETTERS, 2003, 90 (18) :4
[32]   POSITION OF URIDINE THIATION - IDENTIFICATION OF MINOR NUCLEOSIDES FROM TRANSFER RNA BY MASS SPECTROMETRY [J].
HECHT, SM ;
GUPTA, AS ;
LEONARD, NJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1969, 182 (02) :444-&
[33]   Spiers Memorial Lecture: On the hypothesis of cathodic protection of genes [J].
Heller, A .
FARADAY DISCUSSIONS, 2000, 116 :1-13
[34]   Electron impact ionization energies [J].
Hildenbrand, DL .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2000, 197 :237-242
[35]   FAR-VACUUM-ULTRAVIOLET TRANSMISSION SPECTRUM OF URACIL THIN-FILMS [J].
HOU, PW ;
RAMPLING, RP .
JOURNAL OF APPLIED PHYSICS, 1976, 47 (10) :4572-4573
[36]   IDENTIFICATION AND QUANTIFICATION OF NUCLEIC-ACID BASES IN CARBONACEOUS CHONDRITES [J].
HUA, LL ;
KOBAYASHI, K ;
OCHIAI, EI ;
GEHRKE, CW ;
GERHARDT, KO ;
PONNAMPERUMA, C .
ORIGINS OF LIFE AND EVOLUTION OF THE BIOSPHERE, 1986, 16 (3-4) :226-227
[37]   IONIZATION-POTENTIALS AND DONOR PROPERTIES OF NUCLEIC-ACID BASES AND RELATED COMPOUNDS [J].
HUSH, NS ;
CHEUNG, AS .
CHEMICAL PHYSICS LETTERS, 1975, 34 (01) :11-13
[38]   Intrinsic acidity and redox properties of the adenine radical cation [J].
Hwang, CT ;
Stumpf, CL ;
Yu, YQ ;
Kenttämaa, HI .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 1999, 182 :253-259
[39]   Radical cations of DNA bases: some insights on structure and fragmentation patterns by density functional methods [J].
Improta, R ;
Scalmani, G ;
Barone, V .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2000, 201 (1-3) :321-336
[40]   PHOTOACOUSTIC SPECTRA OF SOME BIOLOGICAL MOLECULES BETWEEN 300 AND 130 NM [J].
INAGAKI, T ;
ITO, A ;
HIEDA, K ;
ITO, T .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1986, 44 (03) :303-306