Cell Biology Commons^™

Characterization Of Two Temperature-Sensitive Mutants Of Escherichia Coli Exhibiting An Altered L22 Ribosomal Protein, Bonnie A. Burnette-Vick

Electronic Theses and Dissertations

Analysis of E. coli strains SK1047 and SK1048 have shown them to be temperature-sensitive, protein-synthesis deficient. An alteration in ribosomal protein L22 was detected in both strains using two dimensional gel electrophoresis. Protein L22 was purified from both strains by reversed phase high performance liquid chromatography and from two dimensional electrophoretic gels. Purified ribosomal protein L22 was labeled by reductive methylation and used in 23S RNA binding assays with and without ribosomal protein L4. At the permissive temperature, protein L22 from SK1047 bound less efficiently than the control while protein L22 from SK1048 bound as efficiently as the control. At …

The Submembrane Machinery For Nicotinic Acetylcholine Receptor Clustering, S. C. Froehner

Dartmouth Scholarship

No abstract provided.

The Electrical Response Of Maize To Auxin, Hubert Felle, Winfried Peters, Klaus Palme

Winfried S. Peters

Mouse Mast Cell Proteases: Induction, Molecular Cloning, And Characterization, Wei Chu

Electronic Theses and Dissertations

Tryptase, a mast cell-specific serine protease with trypsin-like specificity, has been identified in a mouse mast cell line (ABFTL-6) based on it's enzymatic activity, inhibition properties, and cross-reactivity to a human mast cell tryptase antibody. The effects of fibroblast-conditioned medium and sodium butyrate on ABFTL-6 mast cell differentiation and tryptase expression have been examined. ABFTL-6 mouse mast cells undergo phenotypic changes upon culturing in media supplemented with fibroblast-conditioned media at 50% or 1 mM sodium butyrate. The induced cells increased in size, had larger and more metachromatic cytoplasmic granules, and increased their total cellular protein about four-fold. Tryptase activity increased …

Fertilization And Mouse Embryo Development In The Presence Of Midazolam, Maria Leavitt

Biological Sciences Theses & Dissertations

The development of mouse embryos in vitro has provided a unique opportunity for the study of cellular differentiation and the influence of various agents on differentiation. Midazolam is administered for conscious sedation in the recovery of human ova. In the Norfolk IVF Program, midazolam is found in varying concentrations in follicular fluid. Mouse embryo formation and development has been used to test midazolam's effect on fertilization and early development as a model of human in vitro fertilization and development. Midazolam' s effects were studied using varying doses of midazolam on (1) in vivo fertilization and subsequent cell division, and (2) …

Cloning And Immunogenicity Of A Chlamydia Trachomatis 36 Kilodalton Recombinant Gene Product In Escherichia Coli, Hector Rivera

Theses Digitization Project

No abstract provided.

Cell Surface-Binding Sites For Progesterone Mediate Calcium Uptake In Human Sperm, Peter F. Blackmore, Joseph Neulan, Frank Lattanzio, Stephen J. Beebe

Bioelectrics Publications

Recent studies (e.g. Blackmore, P. F., Beebe, S. J., Danforth, D. R., and Alexander, N.) (1990) J. Biol. Chem. 265, 1376-1380) have shown that in human sperm, progesterone produces a rapid increase in intracellular free calcium ([Ca2+]i) and an induction of the acrosome reaction (e.g. Osman, R. A., Andria, M. L., Jones, A. D., and Meizel, S. (1989) Biochem. Biophys. Res. Commun. 160, 828-833). In this study, the location of progesterone receptors on the cell surface of human sperm was identified using progesterone immobilized on bovine serum albumin (BSA) (progesterone 3-(O-carboxymethyl)oxime:BSA) as well as progesterone and its 3-O-carboxymethyloxime derivative. Using …

Photoreactivation Of Uv-Induced Damage In G1 Phase Xenopus Cells That Leads To A Sister Chromatid Exchanged And Cell Death, Dawn Laswell, Jennifer Barber, H. Gaston Griggs

Journal of the Arkansas Academy of Science

Experiments were conducted with the A87 Xenopus tissue culture cell line which centered on use of the line's efficient photoreactivation (PR) mechanism to: (1) determine the extent to which sister chromatid exchanges (SCEs), induced by exposing early G1 phase cells to low UV fluenced, are photoreactivable, and (2) determine the extent to which the photoreactivable SCEs resulting from these low UV fluences constitute lethal lesions. For the first determination, UV fluences - SCE frequency relations and UV fluence + PR fluence - SCE frequency relations were established for UV fluences in the range 0-12 J/m2 and a single PR fluence …