TY - JOUR
T1 - Ir vibrational CD in model deoxyoligonucleotides
T2 - Observation of the B → Z phase transition and extended coupled oscillator intensity calcuations
AU - Gulotta, Miriam
AU - Goss, Dixie J.
AU - Diem, Max
PY - 1989/12
Y1 - 1989/12
N2 - The first observation of ir vibrational CD (VCD) in small model DNA molecules is reported. The VCD signals in the 1550–1750‐cm−1 spectral region, which originate from coupling of carbonyl stretching modes of the nucleic acid bases, are found to be sensitive to the handedness of the polymer helix. The formalism to calculate VCD intensities of polymers is developed from the exciton model derived earlier by Tinoco [(1963) Radiation Res. 20, 133; (1960) J. Chem. Phys. 33, 1332; (1964) J. Am. Chem. Soc. 86, 297] and Schellman and co‐workers [(1975) Biopolymers 14, 173; (1969) J. Phys. Chem. 73, 28]. The resulting equations, which are a direct extension of the dimeric case known as the “coupled oscillator,” are used in model calculations of the helical polymers.
AB - The first observation of ir vibrational CD (VCD) in small model DNA molecules is reported. The VCD signals in the 1550–1750‐cm−1 spectral region, which originate from coupling of carbonyl stretching modes of the nucleic acid bases, are found to be sensitive to the handedness of the polymer helix. The formalism to calculate VCD intensities of polymers is developed from the exciton model derived earlier by Tinoco [(1963) Radiation Res. 20, 133; (1960) J. Chem. Phys. 33, 1332; (1964) J. Am. Chem. Soc. 86, 297] and Schellman and co‐workers [(1975) Biopolymers 14, 173; (1969) J. Phys. Chem. 73, 28]. The resulting equations, which are a direct extension of the dimeric case known as the “coupled oscillator,” are used in model calculations of the helical polymers.
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U2 - 10.1002/bip.360281202
DO - 10.1002/bip.360281202
M3 - Article
C2 - 2605309
AN - SCOPUS:0024435557
SN - 0006-3525
VL - 28
SP - 2047
EP - 2058
JO - Biopolymers
JF - Biopolymers
IS - 12
ER -