The synthesis of spermine derivatives (11), RlR2R3~(CH2)3~RlR~(CH~)~l~.4);, and spermidine derivatives (111), R ~R ~R ~~( C H ~) , ~; R ~R P ( C H Z ) , ~R I R Z R , . ~~,are reported. The effects of these salts on the helix-coil transition of r.4-rU and rI-rC helices were examined. Increasing the s
Induction of helicity in polyuridylic acid and polyinosinic acid by silver ions
✍ Scribed by Y. A. Shin; G. L. Eichhorn
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1980
- Tongue
- English
- Weight
- 781 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
Silver ions binding to poly(U) and poly(I) produce highly ordered multistranded helices under conditions which would otherwise lead to random coils. Evidence for helicity comes from the hypochromicity and high ellipticity generated in the polymers by Ag^+^ binding, as well as from x‐ray studies and from the cooperativity of the Ag^+^ complexing reaction. Continuous variation studies show that both polymers form 1:1 and 2:1 polymer–Ag^+^ complexes. Low pH favors the 1:1 complex with poly(U) and the 2:1 complex with poly(I); the reverse is true at high pH. Ag^+^ binding and proton‐release experiments make it clear that at low pH, unprotonated electron‐donor groups are complexed preferentially, but that at high pH, Ag^+^ readily displaces H^+^ from protonated groups. In poly(I) the unprotonated donor is N(7), leading at low pH to a 2:1 complex containing N(7)‐Ag‐N(7) bonds; at high pH, proton release from N(1) leads to a 1:1 complex containing N(1)‐Ag‐O bonds. In poly(U) there is no unprotonated donor; the low‐pH 1:1 complex involves deprotonation of only one N(3) per bound Ag^+^, leading to N~3~‐Ag‐O bonding, while high pH causes deprotonation of two N(3) per Ag^+^ and a 2:1 N(3)‐Ag‐N(3) complex. Thus silver ions react with the nucleotide bases in chemically predictable ways, and the formation of different Ag–nucleotide bonds leads to different multiple‐helix structures.
📜 SIMILAR VOLUMES
An error in Table I11 listed the ratio of the intensity of the Raman band at 811 cm-l to that at 1098 cm-1 in the poly I-poly C complex as 1.5. This value should have been 1.6. The average maximum value of this ratio for the three helices which can be reversibly ordered in the A form (poly I-poly C,
## Abstract The Raman spectra of the double helical complexes of poly C–poly G and poly I–poly C at neutral p^H^ are presented and compared with the spectra of the constituent homopolymers. When a completely double‐helical structure is formed in solution a strong sharp band at 810–814 cm^−1^ appea
## Abstract The ability of specific synthetic polyelectrolytes to act as mitogens for quiescent normal human fibroblasts in cultures is described. Of several acidic polymers tested, polyinosinic acid\*polycytidyli acid (poly I \*poly C) and dextran sulfate were the most effective in stimulating ^3^