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- BookEllen Hsu, Louis Du Pasquier.Contents:
Evolution of immunity and pathogens
A host-pathogen interaction reduced to first principles: Antigenic variation in T. brucei
Antigenic variation in Plasmodium falciparum
Polymorphic mucin-like proteins in Schistosoma mansoni, a variable antigen and a key component of the compatibility between the schistosome and its snail host
Fibrinogen-related proteins (FREP) in mollusks
Somatic and germline diversification of a putative immunoreceptor within one phylum: Dscam in arthropods
An immune effector system in the Protochordate gut sheds light on fundamental aspects of vertebrate immunity
Variable lymphocyte receptors: a current view
Antibody repertoire in fish
Unique features of fish immune repertoires: particularities of the adaptive immunity within the largest group of vertebrates
The evolution and structure of atypical T cell receptors
Diversification of the primary antibody repertoire by AID-mediated gene conversion
Antibody isotype switching in vertebrates.Access via Results and problems in cell differentiation ; 2015; 57LocationVersionCall NumberItems - ArticleMaeda A.Biochim Biophys Acta. 1977 Jan 03;474(1):30-43.A fraction containing a variety of low molecular weight substances was extracted into 80% aqueous acetone from both a colicin E2-treated cell culture of Escherichia coli and an untreated one. The extract was divided into five fractions by Sephadex G15 chromatography. One of them, Fraction B, was separated into three subfractions by Sephadex G10 chromatography. Two subfractions, Fraction BI and Fraction BII, were further fractionated by several chromatographic systems. DNA was incubated with an aliquot from each of these fractions and was then analyzed by sedimentation in an alkaline sucrose density gradient. The activity which caused a decrease in the sedimentation coefficient of the DNA was found in some of these fractions. The activity from colicin E2-treated cells was compared with that from untreated ones. It was revealed that colicin E2 induces some increases in the activity toward DNA in one of the subfractions, Fraction BI, and also causes the appearance of a new species in another fraction, Fraction BII, which potentiates the activity in Fraction BI. These colicin E2-induced changes appeared at 5 min after the addition of colicin E2. The possible significance of such reactions for the action of colicin E2 are discussed.