Affiliation:
1. Departemer to de Física Sección Biofísica Facultad de Ciencias Físicas y Matemáticas. Universidad de Chile
Abstract
The interaction of L-aromatic aminoacids with bases and nucleosides is described.
Of these, ʟ-tryptophan interacts more strongly with bases and nucleosides as indicated by nuclear magnetic resonance, circular dichroism and solubility measurements.
A possible ring-ring type interaction between the aminoacid and bases or nucleosides is proposed; this interaction being such that the hydrodinamic behaviour of the DNA molecule is unchanged.
Ultra violet irradiated DNA is protected by ʟ-tryptophan. A mechanism of energy transfer from the DNA to tryptophan trough triplet-triplet states is discussed.
Cited by
13 articles.
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