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1.
Phys Chem Chem Phys ; 19(30): 19815-19821, 2017 Aug 02.
Artigo em Inglês | MEDLINE | ID: mdl-28657621

RESUMO

Understanding how energetic charged particles damage DNA is crucial for improving radiotherapy techniques such as hadron therapy and for the development of new radiosensitizer drugs. In the present study, the damage caused by energetic particles was simulated by measuring the action of extreme ultraviolet (XUV) attosecond pulses on the DNA building blocks thymine and thymidine. This allowed the ultrafast processes triggered by direct ionization to be probed with an optical pulse with a time resolution of a few femtoseconds. By measuring the yields of fragment ions as a function of the delay between the XUV pulse and the probe pulse, a number of transient processes typically lasting 100 femtoseconds or less were observed. These were particularly strong in thymidine which consists of the thymine base attached to a deoxyribose sugar. This dynamics was interpreted as excited states of the cation, formed by the XUV pulse, rapidly decaying via non-adiabatic coupling between electronic states. This provides the first experimental insight into the mechanisms which immediately proceed from the action of ionizing radiation on DNA and provides a basis on which further theoretical and experimental studies can be conducted.


Assuntos
Dano ao DNA/efeitos da radiação , DNA/química , Radiação Ionizante , Timidina/química , Timina/química , DNA/metabolismo , Espectrometria de Massas , Fatores de Tempo
2.
Science ; 346(6207): 336-9, 2014 Oct 17.
Artigo em Inglês | MEDLINE | ID: mdl-25324385

RESUMO

In the past decade, attosecond technology has opened up the investigation of ultrafast electronic processes in atoms, simple molecules, and solids. Here, we report the application of isolated attosecond pulses to prompt ionization of the amino acid phenylalanine and the subsequent detection of ultrafast dynamics on a sub-4.5-femtosecond temporal scale, which is shorter than the vibrational response of the molecule. The ability to initiate and observe such electronic dynamics in polyatomic molecules represents a crucial step forward in attosecond science, which is progressively moving toward the investigation of more and more complex systems.


Assuntos
Elétrons , Fenilalanina/química , Íons/química , Estrutura Molecular , Fatores de Tempo
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