[Purification of biomolecules by the method of the expanded bed adsorption chromatography. III. Method optimization. Aplications].

This review introduces the principles of the expanded bed adsorption (EBA) and serves as a practical guide to the use STREAMLINE adsorbent and columns available on the market. Critical operational parameters will be discussed as well as the principles for the method design and optimization that will ensure maximum operation of this unique unit. The review is illustrated with the examples of different types of biological molecules which have been purified when using the expanded bed adsorption.

[Purification of biomolecules by the method of adsorptional chromatography in the expanded bed. I. Principles of the method]. / Ochistka biomolekul metodom adsorbtsionnoi khromatografii v rasshirennom cloe. I. Printsipy metoda.

Principles the Expanded Bed Adsorption (EBA) have been described in the survey. The paper also deals with critical operation parameters, principles of the method design and optimization, which will guarantee maximum operation of this unique operation stage. All these problems have been discussed. The survey is illustrated by the examples of various types of biological molecules which have been purified using EBA.

[Biomoleculs purification by the method of the expanded bed adsorption chromatography. II. Design of the experiment]. / Ochistka biomolekul metodom adsorbtsionnoi khromatografii vo vzveshennom sloe. II. Proektirovanie éksperimenta.

This review introduces the principles of the Expanded Bed Adsorption (EBA) and serves as a practical guide to the use of STREAMLINE adsorbent and columns available on the market. Critical operating parameters will be discussed as well as principles for the method design and optimization which will ensure maximum exploitation of this unique operation stage. The review is illustrated with examples of different types of biological molecules which have been purified using Expanded Bed Adsorption.

Modification of lipid composition of neuroblastoma C1300 N18 cells with liposomes alters the cholesterol content.

Cell incubation with lecithin-cholesterol liposomes (1:1 mol/mol) caused enhancement of the cholesterol content. The level of cholesterol esters of total and phospholipid unsaturated fatty acids increased in cholesterol enriched cells. Simultaneously the amount of saturated fatty acids decreased and lysophosphatidylcholine appeared in the cells. On the contrary, cell incubation with lecithin liposomes resulted in cholesterol depletion. This effect was accompanied by a decrease of cholesterol esters, of total and phospholipid unsaturated fatty acids. The content of saturated fatty acids was raised in cells with reduced amount of cholesterol. The quantity of N-acylphosphatidylethanolamine and N-acylethanolamine, lipids newly found in neuroblastoma cells, also changed in cells with modified content of cholesterol. The physiological role of cell response to the changes of cholesterol level is discussed.

[Identification and properties of insulin receptors in neuroblastoma C 1300 N 18 cells in various functional states]. / Identifikatsiia i svoistva insulinovykh retseptorov v kletkakh neiroblastomy C 1300 N 18 pri razlichnykh funktsional'nykh sostoianiiakh.

The presence of insulin receptors in neuroblastoma C 1300 N18 cells was shown by the method of the [125I]insulin binding with cells as well as by the electron-cytochemical methods based on the analysis of the binding of colloid gold-labelled insulin and of agglutinin of wheat embryos with the surface of plasma membrane. It is established that the number and distribution of insulin receptors depend on the functional state of cells. Expression of receptors on the membrane increases after 5'-deoxyuridine-induced differentiation of cells. Due to changes in the lipid composition of cells caused by the incubation with lecithin-cholesterol liposomes (an increase in the content of cholesterol and its esters, as well as of unsaturated fatty acids and appearance of lysolecithin) the quantity of insulin receptors decreases and cell membranes are damaged. The lowering insulin regulation is not observed for insulin receptors of the neuroblastoma C 1300 N18 cells.