Structure and physicochemical properties of diastereomeric isomers of ApA

Nucleic Acids Res Suppl. 2003:(3):41-2. doi: 10.1093/nass/3.1.41.

Abstract

Heterochiral ApAs (ALpAD and ADpAL) together with homochiral D-(ApA) and L-(ApA) were synthesized and their helical structures were investigated by using spectroscopic techniques. The results indicate that the chirality of the 3'-end residue is the primary determinant for the helical sense of adenylyl-(3'-5')-adenosine (ApA).

MeSH terms

  • Circular Dichroism
  • Dinucleoside Phosphates / chemistry*
  • Nucleic Acid Conformation
  • Spectrophotometry, Ultraviolet
  • Stereoisomerism

Substances

  • Dinucleoside Phosphates
  • adenylyl-(3'-5')-adenosine