The main task of this investigation was the clearing of some aspects of Melafen influence on the structural properties of membrane bounded proteins and lipids. Melafen (melamine salt of bis (oximethyl) phosphinic acid) is applied in agriculture, as strong plant growth regulator. Melafen was used as aqua solutions, at wide concentration’s region at all our investigations. The isolated from blood erythrocytes, erythrocyte’s ghost were used as the experimental objects. The Melafen interactions with membrane bounded proteins at the erythrocyte’s ghost were tested by the differential scanning microcalorymetry (DSC) method. The application of DSC allowed us to receive the structural data of protein microdomains organization at erythrocyte’s ghost membranes. We did not reveal any noticeable structural changes of the proteins of erythrocyte ghost membranes under the concentrations of Melafen, when concentrations of Melafen were so much bigger, than concentrations of Melafen, which are used at crop production. The Melafen actions to the protein-lipid interrelationships were tested by registrations of the microviscosity of isolated native erythrocytes. The using of electron spin resonance method (ESR) with introduction of spin-labelled probes to erythrocytes allowed us to receive some structural data of protein -lipid organization at the different depths of erythrocyte’s membranes (2-4 Å; 4-8 Å). The applauding of spectral method for registration of hemolysis degree, allowed us to receive some data about Melafen influences to membrane resistance under the bed environment, when the hypo- and hyper-osmolarity existed. We concluded that Melafen has not any destruction’s influences to the membranes bounded proteins under the concentrations that activate the plant growth. But Melafen had essential influencing to the structural and functional properties of membrane bounded proteins when the bigger concentrations.
Melafen, erythrocyte, erythrocyte ghost, differential microcalorymetry, microviscosity, hemolysis, мелафен, эритроциты, тени эритроцитов, дифференциальная сканирующая микрокалориметрия, микровязкость, гемолиз
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