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Featured researches published by Ivo Frič.


Biochemical and Biophysical Research Communications | 1972

Correlation between polarographic reducibility and circular dichroism of DNA at submelting temperatures

Emil Paleček; Ivo Frič

Abstract The properties of calf-thymus DNA were studied in dependence on temperature with the aid of circular dichroism, pulse polarography, and spectrophotometry. In the region of submelting temperatures the positive CD band amplitude of DNA increased linearly with rising temperature. The polarographic reducibility of DNA grew parallel to the increase of the positive CD band. It has been concluded that the temperature rise in the submelting zone results in changes of DNA conformation. The regions of the DNA molecule with changed conformation are, in comparison with native DNA, more opened, while stacking of bases is not substantially influenced.


Journal of Protein Chemistry | 1990

Effects of conformational constraint in 2- and 8-cycloleucine analogues of oxytocin and [1-penicillamine] oxytocin examined by circular dichroism and biosassay

Ivo Frič; Jan Hlaváček; Todd W. Rockway; W. Y. Chan; Victor J. Hruby

The analogues of oxytocin and [1-penicillamine]oxytocin, containing a cycloleucine (Cle) residue in position 2 or 8, were investigated by means of circular dichroism measurements in different solvents, and the results examined in terms of their biological activities. A cycloleucine residue in position 2 substantially reduces the free conformational space of the hormone 20-membered ring moiety (including the disulfide group), and stabilizes a conformation which is close to one of the possible conformations of oxytocin and involves a β-turn. In position 8, the Cle residue affects the conformation of the Tyr2 side chain, apparently forcing it away from the space above the 20-membered disulfide ring. However, it does not appear that the Cle residue has any significant effect on the overall backbone conformation of the hormone. The steric effect of the penicillamine residue in position 1 on the conformation of the disulfide group and Tyr2 side chain from previous investigations is further confirmed. The synthesis and biological potency of [1-penicillamine, 8-cycloleucine]oxytocin is described. This analogue exhibits a strong inhibitory effect on the uterotonic activity of oxytocinin vitro. It also inhibited the vasopressor response to vasopressin.


Biophysical Chemistry | 1975

Basic polypeptides as histone models: circular dichroism of complexes of model polypeptides with DNA.

J. Šponar; Ivo Frič; Karel Bláha

Circular dichroism (CD) was used to study the complexes of DNA (in 0.15M NaCl) with two polypeptides considered as models of the histone molecules. CD spectra in the region of DNA absorption were studied with respect to the concentration used for annealing and to the molecular weight and composition of the DNA used. The properties of supernatants after centrifugation of aggregated complexes were examined. The effect of selectively bound antibiotics (actinomycin D and netropsin) on CD sprectra of complexes was investigated. The induced CD of proflavine molecules bound to DNA in the various complexes was also studied. It was concluded that changes in the CD spectra of DNA in complexes with the polypeptides are due to the formation of chiral superstructures, even if some conformational changes of DNA molecules themselves may also be decisive in some cases. The superstructure is affected by the composition of DNA, the role of (G + C) rich segments being particularly important.


Collection of Czechoslovak Chemical Communications | 1974

Chiroptical properties of carba-analogues of oxytocin: Conformational considerations

Ivo Frič; M. Kodíček; Karel Jošt; Karel Bláha


Collection of Czechoslovak Chemical Communications | 1974

Synthesis and circular dichroism of some analogues of deamino-1-carba-oxytocin with modifications of the amino-acid residue in position 2

Ivo Frič; M. Kodíček; Ž. Procházka; Karel Jošt; Karel Bláha


International Journal of Peptide and Protein Research | 2009

Conformationally restricted analogs of oxytocin; stabilization of inhibitory conformation

Michal Lebl; Patricia S. Hill; Wieslaw Kazmierski; Lenka Kárászová; Jiřina Slaninová; Ivo Frič; Victor J. Hruby


Collection of Czechoslovak Chemical Communications | 1976

Synthesis and properties of tuftsin, L-threonyl-L-lysil-L-prolyl-L-arginine

J. Vičar; Vladimír Gut; Ivo Frič; Karel Bláha


Collection of Czechoslovak Chemical Communications | 1979

Modified factor analysis of the circular dichroism spectra, applied to a series of cyclodipeptides containing L-proline

Petr Pančoška; Ivo Frič; Karel Bláha


Collection of Czechoslovak Chemical Communications | 1977

Chiroptical properties of 4-azatricyclo[4,4,0,0 3,8 ]decan-5-one - A lactam with a non-planar cis -amide group

Ivo Frič; Petr Maloň; Miloš Tichý; Karel Bláha


Collection of Czechoslovak Chemical Communications | 1980

The optically active 3-ferrocenylalanine and its application in peptide chemistry

Jan Pospíšek; Štefan Toma; Ivo Frič; Karel Bláha

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Karel Bláha

Czechoslovak Academy of Sciences

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Petr Maloň

Academy of Sciences of the Czech Republic

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Karel Jošt

Czechoslovak Academy of Sciences

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Jan Hlaváček

Academy of Sciences of the Czech Republic

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Miloš Tichý

Academy of Sciences of the Czech Republic

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Tomislav Barth

Academy of Sciences of the Czech Republic

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Miloš Buděšínský

Academy of Sciences of the Czech Republic

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Jorga Smolíková

Czechoslovak Academy of Sciences

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Vladimír Gut

Czechoslovak Academy of Sciences

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