Thymine Dimerization in DNA Is an Ultrafast Photoreaction
Pyrimidine dimer
Thymine
Picosecond
Ultraviolet
Quantum yield
Ultraviolet light
DOI:
10.1126/science.1135428
Publication Date:
2007-02-03T07:58:48Z
AUTHORS (9)
ABSTRACT
Femtosecond time-resolved infrared spectroscopy was used to study the formation of cyclobutane dimers in all-thymine oligodeoxynucleotide (dT) 18 by ultraviolet light at 272 nanometers. The appearance marker bands spectra indicates that are fully formed ∼1 picosecond after excitation. ultrafast this mutagenic photolesion points an excited-state reaction is approximately barrierless for bases properly oriented instant absorption. low quantum yield photoreaction proposed result from infrequent conformational states unexcited polymer, revealing a strong link between conformation before absorption and photodamage.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (40)
CITATIONS (486)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....