Method for Making Mature Insulin Polypeptides
US-2016115216-A1 · Apr 28, 2016 · US
US11046742B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11046742-B2 |
| Application number | US-201716097572-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 19, 2017 |
| Priority date | Apr 29, 2016 |
| Publication date | Jun 29, 2021 |
| Grant date | Jun 29, 2021 |
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Provided are a fusion protein having a CCL3 variant with improved in vivo persistency, protein stability and pharmacological activity and a use thereof, more particularly, a fusion protein comprising a CCL3 variant and an immunoglobulin Fc region and a use thereof as a therapeutic agent for lymphopenia, cancer or infection, in which an N-terminal amino acid of a wild-type CCL3α or CCL3β is deleted and an amino acid at a specific position is substituted with a different amino acid at the same position of the wild-type CCL3α or CCL3β in the CCL3 variant.
Opening claim text (preview).
What is claimed is: 1. A fusion protein comprising a variant of CC type ligand 3β (CCL3β) and an immunoglobulin Fc region: wherein the CCL3β variant comprises the sequence of SEQ ID NO: 4 wherein the CCL3β variant is linked to an immunoglobulin Fc region through a linker comprising the sequence of SEQ ID NO: 5, and wherein the immunoglobulin Fc region comprises the sequence of SEQ ID NO: 14. 2. A nucleic acid encoding the fusion protein according to claim 1 . 3. A vector comprising the nucleic acid according to claim 2 . 4. A cell transformed by the vector according to claim 3 . 5. A method of preparing a fusion protein according to claim 1 , said method comprising: (a) culturing a cell transformed by a vector comprising a nucleic acid encoding said fusion protein; and (b) collecting the fusion protein from the cultured cell. 6. A method for treating a cancer comprising administering a pharmaceutical composition comprising the fusion protein according to claim 1 . 7. The method according to claim 6 , wherein the composition is administered in combination with radiation treatment. 8. The method according to claim 6 , wherein the composition is administered to assist radiation treatment.
Alpha-chemokines, e.g. NAP-2, ENA-78, GRO-alpha/MGSA/NAP-3, GRO-beta/MIP-2alpha, GRO-gamma/MIP-2beta, IP-10, GCP-2, MIG, PBSF, PF-4, KC · CPC title
Chemokines, e.g. RANTES · CPC title
the peptide or protein in the drug conjugate being a cytokine, e.g. IL2, chemokine, growth factors or interferons being the inactive part of the conjugate · CPC title
Non-immunoglobulin-derived peptide or protein having an immunoglobulin constant or Fc region, or a fragment thereof, attached thereto · CPC title
DNA or RNA fragments; Modified forms thereof (DNA or RNA not used in recombinant technology, C07H21/00); {Non-coding nucleic acids having a biological activity} · CPC title
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