Fractionation of tyrosine-rich proteins from oxidized wool by ion-exchange chromatography and preparative electrophoresis.
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Biomedical subjects
Publications and source records attributed to H Brunner.
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Lesions in Mycoplasma pneumoniae membranes were produced by antibody and either human or guinea pig complement and were observed by electron microscopy after negative staining. These defects measured approximately 9.0 to 10.0 nm in diameter-slightly more for human complement than for guinea pig complement. The development of these small lesions was accompanied by a decrease in the viability of the organism.
After experimental infection with Mycoplasma pneumoniae, 42% of 67 volunteers developed a threefold or greater rise in antibody in nasal secretions as measured by radioimmunoprecipitation. Development of an antibody increase in sputum was detected more often, i.e., in 73% of the volunteers. Each of the antibody increases involved immunoglobulin (Ig) A. Twelve rises in IgG antibody were detected in the specimens which exhibited a rise in IgA antibody. In almost every instance the rise in IgA antibody exceeded that seen with IgG antibody. Analysis of the response to experimental challenge with M. pneumoniae of volunteers with different levels of preexisting respiratory tract IgA antibody suggested that this secretory antibody was related to host resistance to M. pneumoniae disease. Further, respiratory tract IgA antibody appeared to be more directly related to host resistance than was antibody in serum.
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We describe a system devised to overcome the tendency of fungal mycelium grown in continuous cultures to adhere to the walls and hamper the outflow of the fermentation vessel, with resulting difficulties in attainment of true steadystate conditions.
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