Biochimica et Biophysica Acta (BBA) - General Subjects
A vegetalizing inducing factor isolation and chemical properties
Abstract
A vegetalizing factor which induces the formation of endodermal and mesodermal organs in amphibian gastrula ectoderm was purified from chicken embryos. Preparative sodium dodecyl sulfate polyacrylamide electrophoresis and gel permeation chromatography on Sephadex with different eluants were employed. In buffer containing 6 M urea the molecular weight of the factor was estimated to about 28 000–30 000. In buffer containing sodium dodecyl sulfate (SDS) the factor partially dissociates to smaller polypeptide chains. Because an equilibrium between molecules of different size is established, SDS-containing buffers are not suitable preparative purposes. In 50%–70% formic acid the factor completely dissociates into smaller peptide chains (Mr about 13 000–15 000). Furthermore, very little adsorption of the factor to the gel matrices or glass surfaces is observed in formic acid. The final purification can be achieved by high-performance gel permeation chromatography with glycerolpropyltreated silica gel as column packing and 50% formic acid as eluant.
References (11)
- S. Bramhall et al.
Anal. Biochem.
(1969) - H.-P. Geithe et al.
Biochim. Biophys. Acta
(1970) - H.-P. Geithe et al.
Exp. Cell Res.
(1975) - K. Asahi et al.
Wilhelm Roux's Arch.
(1979) - J. Born et al.
Hoppe=Seyler's Z. Physiol. Chem.
(1972)
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