Crispr/cas-related methods and compositions for knocking out c5
US-2024415980-A1 · Dec 19, 2024 · US
US9238010B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9238010-B2 |
| Application number | US-201213976796-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 13, 2012 |
| Priority date | Jan 13, 2011 |
| Publication date | Jan 19, 2016 |
| Grant date | Jan 19, 2016 |
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The present invention includes a composition comprising at least one oleosin-like protein. The present invention also includes a composition comprising a vesicle comprising at least one oleosin-like protein.
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What is claimed is: 1. A composition comprising a protein comprising a sequence that has at least 80% homology to an oleosin-like protein selected from the group consisting of SEQ ID NOs:21-26, and combinations thereof, wherein said protein is capable of self-assembling into a polypeptide vesicle. 2. The composition of claim 1 , wherein said sequence has at least 90% homology to an oleosin-like protein selected from the group consisting of SEQ ID NOs:21-26, and combinations thereof. 3. The composition of claim 2 , wherein said sequence has at least 95% homology to an oleosin-like protein selected from the group consisting of SEQ ID NOs:21-26, and combinations thereof. 4. The composition of claim 1 , wherein a receptor binding motif is attached to the N-terminus or the C-terminus of said sequence via an amide bond. 5. The composition of claim 4 , wherein said motif is selected from the group consisting of SEQ ID NOs:4-6. 6. The composition of claim 1 , wherein at least two residues of said oleosin-like protein are replaced with cysteine residues. 7. The composition of claim 1 , wherein at least one tyrosine residue in said oleosin-like protein is converted to a L-DOPA residue via a chemical reaction. 8. The composition of claim 7 , wherein at least two of said L-DOPA residues are further crosslinked via a chemical reaction. 9. The composition of claim 1 , wherein at least one sequence selected from the group consisting of SEQ ID NOs:8-12 is inserted in said oleosin-like protein (i) at the junction of hydrophilic and hydrophobic segments, or (ii) within the hydrophilic segment. 10. A composition comprising a vesicle, wherein said vesicle comprises a protein comprising a sequence that has at least 80% homology to an oleosin-like protein selected from the group consisting of SEQ ID NOs:21-26, and combinations thereof. 11. The composition of claim 10 , further comprising a compound encapsulated within said vesicle, wherein said compound is selected from the group consisting of a gas, drug, fluorescent dye, radioactive probe, salt, protein, and nucleic acid. 12. The composition of claim 10 , further comprising at least one pharmaceutically acceptable carrier. 13. A composition comprising a protein comprising a peptide sequence as set forth in residues 26-88 of SEQ ID NO:21, wherein said protein is capable of self-assembling into a polypeptide vesicle.
comprising non-phosphatidyl surfactants as bilayer-forming substances, e.g. cationic lipids or non-phosphatidyl liposomes coated or grafted with polymers (lipids as modifying agents {A61K47/543}) · CPC title
Proteins, e.g. albumin, gelatin · CPC title
from plants · CPC title
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title
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