Received in USA 1st Mgust ~63; -rec&ved in UK for publication 6th titober 1969) There has been considerable recent interest in the solution conformation of macrolide antibiotics based upon the reasonable expectation that this knowledge would lead to deeper insight into their chemical, physical and b
Oligonucleotide interactions. III. Circular dichroism studies of the conformation of deoxyoligonucleolides
✍ Scribed by Charles R. Cantor; Myron M. Warshaw; Herman Shapiro
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1970
- Tongue
- English
- Weight
- 869 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0006-3525
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The circular dichroism (CD) spectra of the four usual deoxymononucleosides, all sixteen deoxydinucleotides, and a number of trinucleotides have been measured. The dimer spectra are quite different from the sum of the spectra of their constituent monomers. This indicates the presence of base‐stacked conformations analogous to those found for ribonucleoside diphosphates. The CD spectra of several deoxytrinucleotide diphosphates and single‐strand f 1 DNA can be calculated fairly well by using a semi‐empirical nearest‐neighbor approach. There is little or no effect of terminal phosphate or of salt concentration on the optical properties of most deoxy oligomers. The possibility of simultaneous analysis of mixtures of deoxypurine or deoxypyrimidine sequence isomers has been examined. This seems to be a viable approach for the analysis of purine runs but cannot promise much success for pyrimidine runs.
📜 SIMILAR VOLUMES
It is axiomatic that in circular dichroism studies, knowledge of the absolute configuration allows determination of the conformation, and vice versa (1). The tetracycline antibiotics are -unusually complex from a conformational standpoint, but choice of appropriate conditions allows one to obtain a