Formulation for Co-Administration of Q-GRFT and Tenofovir
US-2024374681-A1 · Nov 14, 2024 · US
US9249234B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9249234-B2 |
| Application number | US-201213622809-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 19, 2012 |
| Priority date | Mar 17, 2010 |
| Publication date | Feb 2, 2016 |
| Grant date | Feb 2, 2016 |
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The invention provides polynucleotides and methods for expressing light-activated proteins in animal cells and altering an action potential of the cells by optical stimulation. The invention also provides animal cells and non-human animals comprising cells expressing the light-activated proteins.
Opening claim text (preview).
What is claimed is: 1. A light-activated protein comprising, in order from amino terminus (N-terminus) to carboxyl terminus (C-terminus): a) a core amino acid sequence at least 95% identical to the sequence shown in SEQ ID NO:3, SEQ ID NO:1, SEQ ID NO:2, or SEQ ID NO:4; b) an endoplasmic reticulum (ER) export signal; and c) a membrane trafficking signal. 2. The light-activated protein of claim 1 , wherein the ER export signal comprises the amino acid sequence FCEYENEV (SEQ ID NO:12). 3. The light-activated protein of claim 1 , wherein the membrane trafficking signal comprises the amino acid sequence KSRITSEGEYIPLDQIDINV (SEQ ID NO:11). 4. The light-activated protein of claim 1 , wherein the core amino acid sequence is at least 95% identical to amino acids 25-265 of SEQ ID NO:2. 5. The light-activated protein of claim 1 , wherein the core amino acid sequence is at least 95% identical to SEQ ID NO:3. 6. The light-activated protein of claim 1 , wherein the core amino acid sequence is at least 95% identical to SEQ ID NO:4. 7. An isolated polynucleotide comprising a nucleotide sequence encoding the light-activated protein of claim 1 . 8. The polynucleotide of claim 7 , wherein the light-activated protein-encoding nucleotide sequence is operably linked to a promoter. 9. The polynucleotide of claim 7 , wherein the promoter is a CaMKIIa promoter. 10. The polynucleotide of claim 7 , wherein the promoter is a synapsin I promoter. 11. The polynucleotide of claim 7 , wherein the polynucleotide is in an expression vector. 12. The polynucleotide of claim 11 , wherein the expression vector is a viral vector. 13. The polynucleotide of claim 12 , wherein the viral vector is an adenoassociated virus vector, a retroviral vector, an adenoviral vector, a herpes simplex virus vector, or a lentiviral vector.
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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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