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At least 1,351 records · Page 75Linked to original sources
PubMed1994

Two-chain bacteriorhodopsin synthesized by Schizosaccharomyces pombe.

Bacteriorhodopsin (BR), the light-driven proton pump of Halobacterium salinarium purple membrane, was produced in functional form as a two-chain protein by simultaneous expression in the fission yeast Schizosaccharomyces pombe of two separate structural genes, one coding for an aminoterminal BR fragment encompassing the first two transmembrane helices of BR, the other coding for the remainder of the protein. The fragments assemble spontaneously in vivo to yield functional BR which can be purified by immobilized metal ion affinity chromatography.

Amino Acid Sequence↗
PubMed1995

[Interleukin-2 gene cloning and expression in S. cerevisiae].

Mature human Interleukin-2 gene was amplified from IL-2 cDNA by PCR methods. The PCR product was cloned into pUC12 plasmid at Sma I site, then precisely engineered into an intermidiate vector pSK43SB which were digested with Hind III, mung bean nuclease, and Sal I. Added BamH I linker to Cla I site of pSK43SB-IL2 to produce one more BamH I site, then digested pSK43DB-IL2 with restriction enzyme BamH I, the BamH I fragment with an alpha-factor leading sequence, IL2 gene and cycl terminater were produced. It was then cloned into a typical high efficiency episomal expression vector YEpHc8. Human IL-2 protein was purified from supernatant secreted by yeast transformants of YEpHc8-IL2 leading by alpha-factor promoter with IL-2 right translational reading frame and accurate cleavage site. High level expression of IL-2 with highly activity has been purified. A sugar specific silver staining method and 3H sugar labelling experiment has shown the detection of carbohydrate component.

Cloning, Molecular↗
PubMed1996

Engineering human interleukin-6 to obtain variants with strongly enhanced bioactivity.

Interleukin-6 (IL-6) triggers the formation of a high affinity receptor complex with the ligand binding subunit IL-6Ralpha and the signal transducing chain gp130. Since the intracytoplasmic region of the IL-6Ralpha does not contribute to signaling, soluble forms of the extracytoplasmic domain (sIL-6Ralpha), potentiate IL-6 bioactivity and induce a cytokine-responsive status in cells expressing gp130 only. This observation, together with the detection of high levels of circulating soluble human IL-6Ralpha (shIL-6Ralpha) in sera, suggests that the hIL-6-shIL-6Ralpha complex is an alternative form of the cytokine. Here we describe the generation of human IL-6 (hIL-6) variants with strongly enhanced shIL-6Ralpha binding activity and bioactivity. Homology modeling and site-directed mutagenesis of hIL-6 suggested that the binding interface for hIL-6Ralpha is constituted by the C-terminal portion of the D-helix and residues contained in the AB loop. Four libraries of hIL-6 mutants were generated by each time fully randomizing four different amino acids in the predicted AB loop. These libraries were displayed monovalently on filamentous phage surface and sorted separately for binding to immobilized shIL-6Ralpha. Mutants were selected which, when expressed as soluble proteins, showed a 10- to 40-fold improvement in shIL-6Ralpha binding; a further increase (up to 70-fold) was achieved by combining variants isolated from different libraries. Interestingly, high affinity hIL-6 variants show strongly enhanced bioactivity on cells expressing gp13O in the presence of shIL-6Ralpha at concentrations similar to those normally found in human sera.

Antigens, CD↗
PubMedDate not supplied

Ribozyme-mediated suppression of v-myc expression abrogates apoptosis in transformed monocytes.

The product of the c-myc oncogene is an important regulator of both cell proliferation and programmed cell death (apoptosis). We have previously shown that a myelomonocytic cell line termed tEMmyc4, with enforced v-myc expression, underwent apoptosis under growth inhibitory conditions. To further investigate the linkage of v-myc expression to apoptosis in these cells, two hammerhead ribozymes were designed and shown to specifically cleave the v-myc though not c-myc transcript in vitro. These ribozymes were then engineered into the pMAMneo vector under the control of MMTV promoter, transfected into tEMmyc4 cells and clonally selected in G418. Molecular analysis revealed reduction of v-myc expression in ribozyme-expressing cells. This reduction was shown to be associated with abrogation of hormone-induced apoptosis (monitored by gel electrophoresis, flow cytometry and TUNEL assay). These results confirm a direct involvement of v-myc in the induction of apoptosis and indicate a potential means to molecularly control apoptosis using a ribozyme-targeting approach.

Animals↗
PubMed1998

Human dendritic cell (DC)-based anti-infective therapy: engineering DCs to secrete functional IFN-gamma and IL-12.

An imbalance in the Th1- and Th2-type cytokine responses may allow certain microbes to modify the host response to favor their own persistence. We now show that infection/pulsing of human CD34+ peripheral blood hemopoietic progenitor cell-derived dendritic cells (DCs) with Leishmania donovani promastigotes, Histoplasma capsulatum, and Mycobacterium kansasii impairs the constitutive production of IL-12 from these cells. Thus, strategies aimed at modulating a dysregulated Th1/Th2 response to infection would be of great interest. To both augment the host immune response and deliver potent immunomodulatory cytokines such as IL-12 and IFN-gamma, our goal is to develop a therapeutic strategy using genetically modified, microbial Ag-pulsed DCs. Toward developing such immunotherapies, we used retrovirus-mediated somatic gene transfer techniques to engineer human DCs to secrete biologically active IL-12 and IFN-gamma. DCs pulsed with microbial antigens (e.g., leishmania and histoplasma Ags) were capable of inducing proliferative responses in autologous CD4+ lymphocytes. CD4+ lymphocytes cocultured with IL-12-transduced autologous DCs had enhanced Ag-specific proliferative responses compared with CD4+ lymphocytes cocultured with nontransduced or IFN-gamma- transduced DCs. In this cell culture model system we demonstrate that IL-12 has a negative effect on IL-4 secretion that is independent of its ability to induce IFN-gamma secretion. Taken together, these results indicate that IL-12-transduced DCs may be specifically suited in inducing or down-modulating Ag-specific Th1 or Th2 responses, respectively, and thus may be useful as adjunctive therapy in those intracellular infections in which a dominant Th1 response is critical for the resolution of infection.

3T3 Cells↗