Crispr/cas-related methods and compositions for knocking out c5
US-2024415980-A1 · Dec 19, 2024 · US
US9587013B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9587013-B2 |
| Application number | US-201313868387-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 23, 2013 |
| Priority date | Jun 21, 2001 |
| Publication date | Mar 7, 2017 |
| Grant date | Mar 7, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention provides methods for isolating a modified peptide from a complex mixture of peptides, the method comprising the steps of: (a) obtaining a proteinaceous preparation from an organism, wherein the preparation comprises modified peptides from two or more different proteins; (b) contacting the preparation with at least one immobilized modification-specific antibody; and (c) isolating at least one modified peptide specifically bound by the immobilized modification-specific antibody in step (b). The method may further comprise the step of (d) characterizing the modified peptide isolated in step (c) by mass spectrometry (MS), tandem mass spectrometry (MS-MS), and/or MS 3 analysis, or the step of (e) utilizing a search program to substantially match the spectra obtained for the modified peptide during the characterization of step (d) with the spectra for a known peptide sequence, thereby identifying the parent protein(s) of the modified peptide. Also provided are an immunoaffinity isolation device comprising a modification-specific antibody, and antibodies against novel UFD1 and PTN6 phosphorylation sites.
Opening claim text (preview).
What is claimed is: 1. A method of creating a record, the method comprising: (a) obtaining a digested proteinaceous preparation comprising a complex mixture of peptides comprising naturally-occurring post-translationally modified peptides from two or more different proteins; (b) contacting said digested proteinaceous preparation with at least one immobilized post-translational modification-specific antibody; (c) isolating a population of naturally-occurring post-translationally modified peptides specifically bound by said immobilized modification-specific antibody; (d) characterizing said population of modified peptides by mass spectrometry to identify one or more modified peptides of the population; and (e) creating a record comprising information relating to the one or more modified peptides of the population. 2. The method of claim 1 , wherein the mass spectrometry comprises tandem mass spectrometry (MS-MS) and/or MS 3 analysis. 3. The method of claim 2 , wherein the mass spectrometry comprises liquid chromatography-mass spectrometry. 4. The method of claim 1 , further comprising utilizing a search program to substantially match spectra obtained for said modified peptides during the characterization of step (d) with spectra for known peptide sequences, thereby identifying the parent protein(s) of said modified peptides. 5. The method of claim 1 , wherein said digested proteinaceous preparation is obtained from a tissue biopsy cell or a clinical fluid sample. 6. The method of claim 1 , wherein said digested proteinaceous preparation comprises a digested biological sample selected from the group consisting of a digested crude cell extract, a digested tissue sample, a digested serum sample, a digested urine sample, a digested synovial fluid sample, and a digested spinal fluid sample. 7. The method of claim 1 , wherein said digested proteinaceous preparation is obtained using at least one proteolytic enzyme or chemical cleavage. 8. The method of claim 1 , wherein said immobilized antibody is covalently-linked to a chromatography resin or noncovalently-linked to protein-A- or protein-G-agarose. 9. The method of claim 1 , wherein said post-translationally modified peptides comprise phosphorylation modification. 10. The method of claim 1 , wherein said post-translational modification-specific antibody is a monoclonal antibody or a polyclonal antibody. 11. The method of claim 1 , wherein at least one modified peptide isolated in step (c) corresponds to a known marker of disease. 12. The method of claim 1 , wherein said post-translationally modified peptides comprise acetylation, glycosylation, or methylation modification or combinations thereof. 13. The method of claim 1 , wherein said immobilized post-translational modification-specific antibody comprises an antibody that specifically binds a single acetylated amino acid or a single phosphorylated amino acid. 14. A method of creating a record, the method comprising: (a) obtaining a digested proteinaceous preparation comprising a complex mixture of peptides comprising naturally-occurring post-translationally modified peptides from two or more different proteins and fractionating said digested proteinaceous preparation by reversed-phased chromatography to produce a fractionated proteinaceous preparation; (b) contacting said fractionated proteinaceous preparation with at least one immobilized post-translational modification-specific antibody; (c) isolating a population of naturally-occurring post-translationally modified peptides specifically bound by said immobilized modification-specific antibody; (d) characterizing said population of modified peptides by mass spectrometry to identify one or more modified peptides of the population; and (e) creating a record comprising information relating to the one or more modified peptides of the population. 15. The method of claim 14 , wherein the mass spectrometry comprises tandem mass spectrometry (MS-MS) and/or MS 3 analysis. 16. The method of claim 15 , wherein the mass spectrometry comprises liquid chromatography-mass spectrometry. 17. The method of claim 14 , further comprising utilizing a search program to substantially match spectra obtained for said modified peptides during the characterization of step (d) with spectra for known peptide sequences, thereby identifying the parent protein(s) of said modified peptides. 18. The method of claim 14 , wherein said proteinaceous preparation is obtained from a tissue biopsy cell or a clinical fluid sample. 19. The method of claim 14 , wherein said digested proteinaceous preparation comprises a digested biological sample selected from the group consisting of a digested crude cell extract, a digested tissue sample, a digested serum sample, a digested urine sample, a digested synovial fluid sample, and a digested spinal fluid sample. 20. The method of claim 14 , wherein said digested proteinaceous preparation is obtained using at least one proteolytic enzyme or chemical cleavage. 21. The method of claim 14 , wherein said immobilized antibody is covalently-linked to a chromatography resin or noncovalently-linked to protein-A- or protein-G-agarose. 22. The method of claim 14 , wherein said post-translationally modified peptides comprise phosphorylation modification. 23. The method of claim 14 , wherein said post-translational modification-specific antibody is a monoclonal antibody or a polyclonal antibody. 24. The method of claim 14 , wherein at least one modified peptide isolated in step (c) corresponds to a known marker of disease. 25. The method of claim 14 , wherein said post-translationally modified peptides comprise acetylation, glycosylation, or methylation modification or combinations thereof. 26. The method of claim 14 , wherein said immobilized post-translational modification-specific antibody comprises an antibody that specifically binds a single acetylated amino acid or a single phosphorylated amino acid.
against material from animals or humans · CPC title
Affinity chromatography or related techniques based upon selective absorption processes · CPC title
of the antigen-antibody type, e.g. protein A, G or L chromatography · CPC title
against material not provided for elsewhere {, e.g. haptens, metals, DNA, RNA, amino acids} · CPC title
involving peptides or proteins · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.