Highly Purified Colicin E3 Contains Immunity Protein
Author(s) -
Karen S. Jakes,
Norton D. Zinder
Publication year - 1974
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.71.9.3380
Subject(s) - colicin , polyacrylamide gel electrophoresis , sodium dodecyl sulfate , immunity , guanidine , gel electrophoresis , size exclusion chromatography , chemistry , biochemistry , biology , microbiology and biotechnology , escherichia coli , immune system , enzyme , immunology , gene
Colicin E3, even when highly purified, still contains about one molar equivalent of a second protein, “E3 immunity protein.” The two proteins are bound together in a complex that can be dissociated only under strongly denaturing conditions, such as electrophoresis in sodium dodecyl sulfate-polyacrylamide gles or by gel filtration in 6 M guanidine·hydrochloride. Colicin and immunity protein were separated by preparative electrophoresis in sodium dodecyl sulfate-polyacrylamide gels. The immunity protein prepared in this way was shown to be functionally and immunologically identical to immunity protein purified from colicinogenic cells by other methods. Colicin E3 that had been freed of immunity protein was much more active than complexed colicin in inhibiting protein synthesisin vitro .
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