Fringe field-tunable LC refractive index interface for in-plane beam steering applications.

We report on the electrically tunable optical structure based on dual-domain nematic liquid crystal (LC) alignment for in-plane beam steering applications. The device operates due to the total internal reflection of an extraordinary beam at the LC refractive index interface that separates homeotropic and planar-aligned nematics. Patterned electrodes were used in order to switch on the refractive index interface in the bulk of a planar-aligned LC layer.

Electrically controlled spatial-polarization switch based on patterned photoalignment of nematic liquid crystals.

A switching scheme for two orthogonal modes of laser radiation that is based on the total internal reflection effect realized at the interface of two liquid crystal regions with orthogonal director orientations is proposed. To create the photorefractive interface within the bulk of a liquid crystal, an original technique based on self-alignment of azo dye photoalignment and absorbing electrode patterns has been developed. Spatial separation of the orthogonally polarized light beams and their switching (when the positions of reflected and transmitted light beams are switched) due to the voltage applied has been experimentally realized.

Cell death of L-929 cells induced by cytotoxic complex Tag7-Hsp70 is analogous to the death of the same cells induced by TNF-α.

The identification and studying the molecular bases of functioning of new cytotoxic agents finds an important implication in developing drugs for fighting with tumors. While investigating the cytotoxic action of protein complex Tag7-Hsp70 which was opened in our laboratory previously we found that Tag7-Hsp70 demonstrated the same specificity in regard to different tumor target cells as it was for classical cytokine TNF-α. L-929 cells and Jurkat cells appeared to be good targets representing up to 30% of dead cells within a population and HeLa cells--bad targets representing less than 5% of dead cells after 20 h of incubation with either of the cytotoxic agents.

Extracellular HspBP1 inhibits formation of a cytotoxic Tag7-Hsp70 complex in vitro and in human serum.

Tag7 (PGRP-S) was described as an innate immunity protein. Earlier we have shown that Tag7 forms with Hsp70 a stable complex with cytotoxic and antitumor activity. The same complex is formed in and secreted by cytotoxic T-lymphocytes.