IP Library Granted Patent US 10,126,309
Granted Patent B2
US 10,126,309 · App. 14/799,778 · Granted Nov 13, 2018

Method for the detection of an albumin isoform

Inventor: John E. Wiktorowicz (League City, TX)
Assignee: THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEMS
G01N33/6869G01N33/564G01N33/56983G01N33/6851G01N2333/185G01N2333/47G01N2333/4716G01N2333/5428G01N2333/55G01N2333/76G01N2800/26
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,126,309
App. No.
14/799,778
Granted
Nov 13, 2018
Kind
B2
Abstract

The present invention provides methods for detecting, analyzing, and identifying biomolecules used to identifying patient with dengue-like symptom who are at risk of DHF. The inventive method comprises detecting in a sample from a subject dengue infected patient one or more biomarkers selected from the group consisting of IL-10, fibrinogen, C4A, immunoglobulin, tropomyosin, and three isoforms of albumin, and which are used in a predictive MARS model to detect patients with risk of developing DHF.

Claims (13)

1. A sample fractionation method for albumin biomarker identification comprising:

(a) fractionating a sample derived from blood by size exclusion chromatography, wherein the sample has protein/peptide complexes dissociated by denaturation and the sample is spiked with a labeled protein of about 200 amino acid residues for differentiating protein and peptide pools;

(b) collecting a (i) protein pool comprising the fractions preceding the end of the labeled protein peak, and (ii) a peptide pool comprising the fractions after the end of the labeled protein peak and before the free dye peak;

(c) incubating the collected protein pool to allow for renaturation of the collected proteins in the protein pool;

(d) depleting the protein pool by exposing the protein pool to an antibody depletion column and collecting column flow through to produce a depleted sample;

(e) labeling the depleted sample with an uncharged thiol reactive label forming a saturated fluorescence labeled sample;

(f) conducting two dimensional (2D) gel electrophoresis on the saturated fluorescence labeled sample, producing a 2D gel;

(g) imaging the 2D gel and identifying a protein(s) of interest, wherein the protein of interest is an albumin isoform; and

(h) conducting mass spectrometry analysis of the protein(s) of interest.

2. The method of claim 1 , wherein the size exclusion chromatography uses a size exclusion column having a separation range between molecular weights of 3,000 to 70,000 daltons.

3. The method of claim 1 , wherein the spiked labeled protein is a labeled thaumatin.

4. The method of claim 1 , wherein the antibody depletion column is an IgY antibody depletion column.

5. The method of claim 1 , wherein the thiol reactive label is bodipy FL-maleimide.

Assignments (2)
CONFIRMATORY LICENSE Recorded Apr 4, 2022
From: UNIVERSITY OF TEXAS MED BR GALVESTON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 059581/0287 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 23, 2017
From: WIKTOROWICZ, JOHN E.
To: THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 042798/0704 →
Continuity (3)
Continuation 13490360 · Jun 6, 2012
Provisional Application 61493923 · Jun 6, 2011
Related Publication 20150316562A1 · Nov 5, 2015