Biopolym. Cell. 2011; 27(6):442-445.
Structure and Function of Biopolymers
Influence of polymers on lysozyme molecules association
- A. V. Bogatsky's Physico-chemical Institute, NAS of Ukraine
86, Lustdorfskaya dor., Odessa, Ukraine, 65080 - A. A. Chuyko Institute of Surface Chemistry, NAS of Ukraine
17, Generala Naumova Str., Kyiv, Ukraine, 03164
Abstract
Aim. Study of lysozyme molecules behaviour at immobilization in gelatin and carboxymethyl cellulose sodium salt solutions by matrix-assisted laser desorption/ionization (MALDI). Methods. Determination of the activity of lysozyme, both free and entrapped in gelatin and carboxymethyl cellulose sodium salt (Na-CMC) solutions, was conducted by bacteriolytic method. The enzyme interaction with polymers was confirmed by viscometry and mass-spectrometry methods. Results. The occurrence of lysozyme associates in aqueous solution in monomeric and oligomeric forms was shown. A non-valent interaction of the enzyme with solutions of polymers results in the dissociation of oligomeric associates into subunits, which depends on the support nature and mass ratio of lysozyme to polymer. The quantitative retention of immobilized lysozyme hydrolytic activity was established, which favours obtaining mucoadhesive film forms with bacteriolytic action. Conclusions. The lysozyme immobilization by non-valent interactions in gelatin solution and Na-CMC solutions causes dissociation of the enzyme oligomeric structures; a stronger lysozyme coupling with Na-CMC was noted.
Keywords: lysozyme, oligomers, dissociation, gelatin, carboxymethyl cellulose sodium salt, MALDI
Full text: (PDF, in Russian)
References
[1]
Romanovskaya I. I., Davidenko T. I., Dekina S. S., Pashkin I. I., Andronati S. A. Immobilization of biologically active substances with an aim of potential diagnostic and medicinal means creation J. Organic and Pharmaceutical Chemistry 2009 7, N 3 (27) P. 69–78.
[2]
Punitha S., Girish Y. Polymers in mucoadhesive buccal drug delivery system – a review Int. J. Res. Pharm. Sci 2010 1, N 2 P. 170–186.
[3]
Kharenko E. A., Larionova N. I., Demina N. B. Mucoadhesive drug delivery systems (Review) Pharmaceutical Chem. J 2009 43, N 4 P. 21–29.
[4]
Dai G. L., Yu Y., Kang Q., Hu W. R. Studying aggregate in lysozyme solution by atomic force microscope Chinese Chem. Lett 2004 15, N 10 P. 1237–1240.
[5]
Artemova N. V., Kasakov A. S., Bumagina Z. M., Lyutova E. M., Gurvits B. Y. Protein aggregates as depots for the release of biologically active compounds Biochem. Biophys. Res. Commun 2008 377, N 2 P. 595–599.
[6]
Levitsky A. P. Lysozyme instead of antibiotics Odessa: KP OGT, 2005 74 p.
[7]
Bartenev G. M., Frenkel S. Y. Physics of polymers Leningrad: Khimiya, 1990 332 p.
[8]
Binkley S. L., Ziegler C. J., Herrick R. S., Rowlett R. S. Specific derivatization of lysozyme in aqueous solution with Re(CO)3 (H2O)3(+) Chem. Commun. (Camb) 2010 46, N 8 P. 1203– 1205.
[9]
Veis A. The macromolecular chemistry of gelatin Moscow: Pishchevaya promyshlennost’, 1971 480 p.
[10]
Mikhailov O. V. Low-temperature template synthesis in metallgeksatcianoferrat (II) gelatin-immobilized matrix systems (review) Russ. Chem. J 2000 44, N 3 P. 70–79.