Translocation of non-natural chemical entities through anthrax protective antigen pore
US-2015165062-A1 · Jun 18, 2015 · US
US10006916B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10006916-B2 |
| Application number | US-201214005416-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 15, 2012 |
| Priority date | Mar 15, 2011 |
| Publication date | Jun 26, 2018 |
| Grant date | Jun 26, 2018 |
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.
Some aspects of this invention provide reagents and methods for the sensitive, quantitative and simultaneous detection of target analytes in complex biological samples by liquid chromatography tandem mass spectrometry (LC MS/MS). Some aspects of this invention provide affinity reagents encoded with mass reporters for the sensitive and quantitative translation of an analyte of interest into a mass tag. The reagents and methods provided herein have general utility in analyte detection and encoding, for example, in biomolecular profiling, molecular diagnostics, and biochemical encoding.
Opening claim text (preview).
The invention claimed is: 1. A method for the detection of aberrant protease activity in a subject, comprising (a) administering to the subject a pro-diagnostic reagent comprising a set of isotope-coded reporter molecules (iCOREs) each conjugated to a carrier domain, wherein each iCORE comprises a mass tag conjugated to the carrier domain via a cleavable linker, under conditions suitable for cleavage of the cleavable linker by a disease-associated protease in vivo; (b) identifying and/or quantifying the iCOREs in a biological sample obtained from the subject; and (c) determining that the subject has an aberrant protease activity signature based on the iCORES identified in (b). 2. The method of claim 1 , wherein the set of iCORES comprises at least 5 different mass tag-conjugated cleavable linkers. 3. The method of claim 1 , wherein the iCOREs are isobaric. 4. The method of claim 1 , wherein the iCOREs are peptide mass tags. 5. The method of claim 3 , wherein the iCOREs comprise 5-20 amino acid residues. 6. The method of claim 3 , wherein the iCOREs comprise the same amino acid sequence. 7. The method of claim 6 , wherein the iCOREs comprise the amino acid sequence EGVNDNEEGFFSAR (SEQ ID NO: 1). 8. The method of claim 1 , wherein the iCOREs are isotope-labeled. 9. The method of claim 1 , wherein (b) comprises an MS/MS assay. 10. The method of claim 1 , wherein the biological sample is a urine sample. 11. The method of claim 1 , wherein the disease-associated protease is associated with cancer. 12. The method of claim 1 , wherein the disease-associated protease is associated with fibrosis. 13. The method of claim 1 , wherein the set of iCORES comprises at least 6 different mass tag-conjugated cleavable linkers. 14. The method of claim 1 , wherein the set of iCORES comprises at least 7 different mass tag-conjugated cleavable linkers. 15. The method of claim 1 , wherein the set of iCORES comprises at least 8 different mass tag-conjugated cleavable linkers. 16. The method of claim 1 , wherein the set of iCORES comprises at least 9 different mass tag-conjugated cleavable linkers. 17. The method of claim 1 , wherein the set of iCORES comprises 10 different mass tag-conjugated cleavable linkers. 18. The method of claim 1 , wherein the set of iCORES comprises 20 different mass tag-conjugated cleavable linkers.
by chemical synthesis · CPC title
having 12 to 20 amino acids (gastrins C07K14/595; somatostatins C07K14/655; melanotropins C07K14/68) · CPC title
involving labelled substances (G01N33/53 takes precedence) · 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
Methods of protein analysis involving mass spectrometry · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.