Literature DB >> 4093443

Ricin D-saccharide interaction as studied by ultraviolet difference spectroscopy.

N Yamasaki, T Hatakeyama, G Funatsu.   

Abstract

The interaction of ricin D with specific saccharides was investigated by ultraviolet difference spectroscopy. Upon binding to saccharides, ricin D displayed ultraviolet difference spectra with maxima at 280 nm and 288 nm. Such difference spectra suggest that the environment of a tyrosine residue(s) located at or near the saccharide-binding site is changed by the binding of saccharide. In addition to the two positive peaks, a small trough was observed around 300 nm in the complexes with galactose-containing saccharides but not in the complex with N-acetylgalactosamine or galactosamine, suggesting the participation of tryptophan in the binding with galactose-containing saccharides. The magnitude of the difference maxima increased with increasing concentration of saccharides until the binding site was saturated. From the variation of the maximum at 288 nm as a function of saccharide concentration, the association constants were obtained for the binding of saccharides to ricin D at various temperatures and pH's. The saccharide binding of ricin D decreased with increasing temperature and with decreasing pH below pH 6.0. It was suggested that difference maximum at 288 nm observed in the ricin D-saccharide interaction reflects the binding of saccharides to the high-affinity saccharide-binding site of ricin D.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 4093443     DOI: 10.1093/oxfordjournals.jbchem.a135424

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  4 in total

1.  The (QxW)3 domain: a flexible lectin scaffold.

Authors:  B Hazes
Journal:  Protein Sci       Date:  1996-08       Impact factor: 6.725

2.  Effect of physical environment on the conformation of ricin. Influence of low pH.

Authors:  J P Frénoy
Journal:  Biochem J       Date:  1986-11-15       Impact factor: 3.857

3.  Mutational analysis of the carbohydrate-binding activity of the NeuAc(alpha-2,6)Gal/GalNAc-specific type 2 ribosome-inactivating protein from elderberry (Sambucus nigra) fruits.

Authors:  Ying Chen; Pierre Rouge; Willy J Peumans; Els J M van Damme
Journal:  Biochem J       Date:  2002-06-01       Impact factor: 3.857

4.  Galactose recognition by a tetrameric C-type lectin, CEL-IV, containing the EPN carbohydrate recognition motif.

Authors:  Tomomitsu Hatakeyama; Takuro Kamiya; Masami Kusunoki; Sachiko Nakamura-Tsuruta; Jun Hirabayashi; Shuichiro Goda; Hideaki Unno
Journal:  J Biol Chem       Date:  2011-01-19       Impact factor: 5.157

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.