Document Detail


Removal of the side-chain glucose groups from schizophyllan improves the thermal stability of the polycytidylic acid complexes under the physiological conditions.
MedLine Citation:
PMID:  15457435     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Thermal stabilization of the complex between polycytidylic acid [poly(C)] and the modified schizophyllan (SPG) whose hydrophilic side-chain glucose groups are selectively removed utilizing mild Smith-degradation has been investigated. With the decrease in the side-chain glucose groups of schizophyllan, the complex with poly(C) can be considerably stabilized compared with unmodified SPG; for example, the T(m) value after the removal of the side-chain glucose groups from 33.3 (unmodified) to 1.0 is enhanced by 14 degrees C. In addition, the thermal stabilization effect is even operative under the physiological conditions ([NaCl] = 0.15 mol dm(-3)). This effect is exerted owing to the construction of the hydrophobic atmosphere around the complex. Although schizophyllan lost the side-chain glucose groups, it still kept the protection effect of the bound poly(C) chain against RNaseA-mediated hydrolysis as observed for unmodified schizophyllan. The assessment of the cytotoxicity for A375:human malignant melanoma, and HL60:human promyelocytic leukemia revealed that the modified schizophyllan scarcely increases the cytotoxicity. These results indicate that the present modification for schizophyllan is of great significance in a viewpoint to develop the practical gene carriers operative even under the physiological conditions.
Authors:
Kazuya Koumoto; Ryouji Karinaga; Masami Mizu; Takahisa Anada; Kazuo Sakurai; Toyoki Kunitake; Seiji Shinkai
Related Documents :
17076315 - Effect of conditioners on bond durability of resin composite to nd:yap laser-irradiated...
17025065 - Preparation and characterization of polypeptide-stabilized gold nanoparticles.
16921535 - Thermal degradation of environmentally degradable poly(hydroxyalkanoic acid)s.
11395705 - Tensile bond strength of ceramic orthodontic brackets bonded to porcelain surfaces.
3886545 - Comparison of the capacity of two lipid a precursor molecules to express the local shwa...
18823315 - Copper stress induces biosynthesis of octadecanoid and eicosanoid oxygenated derivative...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Biopolymers     Volume:  75     ISSN:  0006-3525     ISO Abbreviation:  Biopolymers     Publication Date:  2004 Dec 
Date Detail:
Created Date:  2004-11-03     Completed Date:  2005-03-07     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0372525     Medline TA:  Biopolymers     Country:  United States    
Other Details:
Languages:  eng     Pagination:  403-11     Citation Subset:  IM    
Copyright Information:
Copyright 2004 Wiley Periodicals, Inc.
Affiliation:
Department of Chemical Processes and Environments, Faculty of Environmental Engineering, The University of Kitakyushu, 1-1 Hibikino, Wakamatsu-ku, Kitakyushu, Fukuoka 808-0135, Japan.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Cell Line, Tumor
Cell Survival
Drug Stability
Glucose / chemistry*
Humans
Hydrolysis
Poly C / chemistry*
Ribonuclease, Pancreatic / chemistry
Sizofiran / chemistry*,  toxicity
Temperature
Chemical
Reg. No./Substance:
30811-80-4/Poly C; 50-99-7/Glucose; 9050-67-3/Sizofiran; EC 3.1.27.5/Ribonuclease, Pancreatic

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  NMR solution structure of a highly stable de novo heterodimeric coiled-coil.
Next Document:  Gelation of gellan gum aqueous solutions studied by polarization modulation spectroscopy.