Polypeptide hormones of the thymus

Claim 1

A highly purified polypeptide named as Thymopoietin I and having the following amino acid sequence: H 2 n-gly-gln-phe-leu-glu-asp-pro-ser-val-leu-thr-lys-glu- lys-leu-lys-ser-glu-leu-val-ala-asn-asn-val-thr-leu-pro-ala-gly-glu- gln-arg-lys-asp-val-tyr-val-gln-leu-tyr-leu-gln-his-leu-thr-ala-val- lys-arg-cooh, said polypeptide existing in the physical form of a powder, said polypeptide having relative mobilities on 7% polyacrylamide disc electrophoresis of 0.3 at a pH of 8.9 with respect to bromophenol blue, and 0.63 at a pH of 4.3 with respect to methyl green, said polypeptide being therapeutically active at concentrations of 0.2-2 nanogram per ml.

Claim 5

A method for the isolation from bovine thymus of the polypeptides Thymopoietin I and Thymopoietin II, which comprises homogenizing bovine thymus in buffered saline solution, heating to a temperature of about 60°-90° C. to complete homogenization, centrifuging and filtering to remove non-homogenized and insoluble materials and provide a resulting solution, subjecting this resulting solution to molecular sizing by contacting with a dialysate membrane of such size as to allow polypeptides to pass through the membrane while excluding materials having molecular weights above about 100,000, passing the resulting solution which passed through the membrane through a second dialysate membrane of such size so as to exclude materials having molecular weights below about 2,000, recovering therefrom a retentate containing materials having molecular weights of about 2,000-100,000 and of reduced volume, fractionating the resulting retentate by molecular exclusion chromatography at least two times by placing in a solution of ammonium bicarbonate and contacting the solution with a cross-linked dextran molecular sieve which totally excludes materials having molecular weights above about 30,000 wherein materials having molecular weights of less than about 1500 will totally permeable and recovering an extract containing materials having molecular weights in the range of about 4,000 to about 12,000, further fractionating the resulting extract by adsorption chromatography by dissolving the extract in a solution 0.001 M to 0.008 M phosphate buffer solution at a pH of about 6.8 and contacting with hydroxy apatite by passage through a column containing the hydroxyl apatite, and separation is effected by differential sticking on the hydroxyl apatite, the active fractions being retarded behind the void volume, collecting the active fractions by lyophilizing and desalting, fractionating to separate two active fractions by contact at least once by ion exchange chromatography by dissolving in a buffer base at a pH of about 10 to 11 and contacting with an anion exchanger comprising beads as the backbone with polymer groups attached thereon wherein the product is retained by the beads, recovering the product fractions by raising the molarity of the solution by linear concentration gradients, lyophilizing and desalting the resulting active fractions on a cross-linked dextran molecular sieve and recovering the purified Thymopoietin I and Thymopoietin II.

Claim 6

A method for the isolation from bovine thymus of the polypeptides Thymopoietin I and Thymopoietin II, which comprises homogenizing bovine thymus in buffered saline solution, heating to a temperature of about 60°-90° C. to complete homogenization, centrifuging and filtering to remove non-homogenized and insoluble materials and provide a resulting solution, subjecting this resulting solution to molecular sizing by contacting with a dialysate membrane of such size as to allow polypeptides to pass through the membrane while excluding materials having molecular weights above about 100,000, passing the resulting solution which passed through the membrane through a second dialysate membrane of such size so as to exclude materials having molecular weights below about 2,000, recovering therefrom a retentate containing materials having molecular weights of about 2,000-100,000 and of reduced volume, fractionating the resulting retentate by molecular exclusion chromatography at least two times by placing in a solution of ammonium bicarbonate and contacting the solution with a cross-linked dextran molecular sieve which totally excludes materials having molecular weights above about 30,000 wherein materials having molecular weights of less than about 1500 will totally permeable and recovering an extract containing materials having molecular weights in the range of about 4,000 to about 12,000, further fractionating the resulting extract by adsorption chromatography by dissolving the extract in a solution 0.001 M to 0.008 M phosphate buffer solution at a pH of about 6.8 and contacting with hydroxy apatite by passage through a column containing the hydroxyl apatite, and separation is effected by differential sticking on the hydroxyl apatite, the active fractions being retarded behind the void volume, collecting the active fractions by lyophilizing and desalting, fractionating to separate two active fractions by contact at least once by ion exchange chromatography by dissolving in a buffer base at a pH of about 10 to 11 and contacting with an anion exchanger comprising beads as the backbone with polymer groups attached thereon wherein the product is retained by the beads, recovering the product fractions by raising the molarity of the solution by linear concentration gradients, lyophilizing and desalting the resulting active fractions on a cross-linked dextran molecular sieve and recovering the purified Thymopoietin I and Thymopoietin II.