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Determination of protein synthesis initiation factor levels in crude lysates of Escherichia coli by a sensitive radioimmune assay

1978; Elsevier BV; Volume: 191; Issue: 2 Linguagem: Inglês

10.1016/0003-9861(78)90424-1

1096-0384

Jörg Howe, Joan Yanov, Laurence Meyer, Kathleen Johnston, John W.B. Hershey,

Protein purification and stability

Antisera specific for protein synthesis initiation factors IF1, IF2, and IF3 were prepared by immunizing rabbits. When crude cell lysates are analyzed by double immunodiffusion or by immunoelectrophoresis, each antiserum forms a single precipitin line antigenically identical to its cognate factor. The antisera do not crossreact with other initiation factors or with ribosomal proteins. A radioimmune assay was developed for each initiation factor by using the specific antisera and radioactive factors prepared by reductive alkylation with [14C]formaldehyde. The assays detect as little as 10 to 30 ng of factor. Initiation factor concentrations were measured in crude Escherichin coli MRE600 extracts prepared from cells grown exponentially in a rich medium. The three initiation factors are present in approximately stoichiometric amounts and comprise about 1% of the cell protein. The molar ratio of initiation factors to ribosomes is about 0.15, which corresponds to the concentration of native ribosomal subunits.