IP Library Granted Patent US 6,998,243
Granted Patent B2
US 6,998,243 · App. 09/845,739 · Granted Feb 14, 2006

Biopolymer marker indicative of disease state having a molecular weight of 1793 daltons

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Quick Facts
Patent No.
US 6,998,243
App. No.
09/845,739
Granted
Feb 14, 2006
Kind
B2
Abstract

The instant invention involves the use of a combination of preparatory steps in conjunction with mass spectroscopy and time-of-flight detection procedures to maximize the diversity of biopolymers which are verifiable within a particular sample. The cohort of biopolymers verified within such a sample is then viewed with reference to their ability to evidence at least one particular disease state; thereby enabling a diagnostician to gain the ability to characterize either the presence or absence of at least one disease state relative to recognition of the presence and/or the absence of the biopolymer.

Claims (13)

1. An isolated biopolymer marker consisting of SEQ ID NO:1.

2. A method for determining in a patient sample, the presence of an isolated biopolymer marker consisting of SEQ ID NO:1 which is linked to congestive heartfailure comprising:

(a) obtaining a sample from a patient;

(b) conducting mass spectrometric analysis on said sample in a manner effective to maximize analysis of peptide fragments contained therein and comparing mass spectrum profiles of said isolated biopolymer marker consisting of SEQ ID NO:1 to mass spectrum profiles of peptides obtained and analyzed from said sample; and

(c) confirming the presence of said isolated biopolymer marker consisting of SEQ ID NO:1 in said sample displaying a peak profile at about 1793 daltons in said mass spectrum profile;

wherein the presence of said isolated biopolymer marker consisting of SEQ ID NO:1 is indicative of a link to congestive heart failure.

3. The method of claim 2 , wherein the sample is an unfractionated body fluid or a tissue sample.

4. The method of claim 2 , wherein said sample is selected from the group consisting of blood, blood products, urine, saliva, cerebrospinal fluid, and lymph.

5. The method of claim 2 , wherein said mass spectrometric analysis is Surface Enhanced Laser Desorption Ionization (SELDI) mass spectrometry (MS).

6. The method of claim 2 , wherein said patient is a human.

7. A kit for determining the presence of an isolated biopolymer marker consisting of SEQ ID NO:1 comprising: (a) a peptide consisting of SEQ ID NO:1, and (b) an antibody that binds to said peptide in a sample from a patient.

8. The kit of claim 7 , wherein said antibody is immobilized on a solid support.

9. The kit of claim 7 , wherein said antibody is labeled.