Publications by authors named "S Mikhalap"

In order to the detection of type-specific IgG to herpes simplex virus type 2 (HSV-2) in human serum or plasma the recombinant analog of HSV-2 glycoprotein G (gG2) was created. To construct an expression vector the DNA fragment with a sequence identical to immunodominant regions of HSV-2 gG2 was cloned into modified vector pET28a containing of the glutation-S-transferase sequence (pET28-GST). Escherichia coli BL21 (DE3) were transformed with the recombinant plasmid.

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Recent scientific research demonstrates that protein kinases of PKD family affect biological features of normal and malignant cells. Differential expression of PKD genes was found in tumors of different histogenesis. These protein kinases could be activated by growth factors, antigen stimulation, and oxidative stress, the processes that usually can be observed during tumor progression.

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The new family of serine/threonine protein kinases D (PKD) belongs to Ca2+/calmodulin-dependent protein kinase group. Here we review with the role of PKDs in the regulation of post-translational modification of cellular proteins. PKDs directly phosphorylate a number of cell signaling molecules, moreover PKDs indirectly regulate histone acetylation and glycosylation of proteins.

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Article Synopsis
  • The study examined the expression, autophosphorylation, and localization of PKD2 in reactive lymph nodes and lymphoid tissue tumors, particularly non-Hodgkin's lymphoma (NHL) and Hodgkin's lymphoma (HL).
  • Specific antibodies were used to analyze tissue samples through immunohistochemical and biochemical methods, revealing PKD2 presence in tonsils and tumor tissues, while PKD1 was absent.
  • Findings indicated that PKD2 expression varies by type of lymphoma, being highest in activated B cell phenotypes and associated with higher levels of cell differentiation and activation.
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The CD150 receptor is expressed on activated T and B lymphocytes, dendritic cells, and monocytes. A TxYxxV/I motif in the CD150 cytoplasmic tail can bind different SH2-containing molecules, including tyrosine and inositol phosphatases, Src family kinases, and adaptor molecules. To analyze CD150-initiated signal transduction pathways, we used DT40 B-cell sublines deficient in these molecules.

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