IP Library Granted Patent US 10,578,623
Granted Patent B2
US 10,578,623 · App. 15/991,892 · Granted Mar 3, 2020

Peptide array quality control

Inventors: Neal Woodbury (Tempe, AZ); Stephen Johnston (Tempe, AZ); Phillip Stafford (Phoenix, AZ)
Assignee: ARIZONA BOARD OF REGENTS OF BEHALF OF ARIZONA STATE UNIVERSITY
G01N33/6845
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Quick Facts
Patent No.
US 10,578,623
App. No.
15/991,892
Granted
Mar 3, 2020
Kind
B2
Abstract

The present application provides arrays for use in immunosignaturing and quality control of such arrays. Also disclosed are peptide arrays and uses thereof for diagnostics, therapeutics and research.

Claims (30)

1. A method for determining quality and fidelity of an in situ synthesized peptide array configured for use in an immunosignature assay, comprising:

obtaining a first binding pattern of the in situ synthesized peptide array, wherein the first binding pattern is obtained from binding with a first sample, the first sample comprising a biological sample from a subject, wherein the in situ synthesized peptide array comprises at least 100 compounds;

obtaining a second binding pattern of an in situ synthesized reference peptide array;

comparing the first binding pattern with the second binding pattern and calculating a correlation value, wherein the comparing comprises a direct peptide-by-peptide comparison between the first and the second binding patterns to evaluate a number of peptides expressing different patterns and a comparison between a binding profile of the first binding pattern and a binding profile of the second binding pattern to evaluate a level of similarity between the binding profiles, wherein each of the binding profiles comprises a distribution of signals measured from a population of at least 2 arrayed compounds; and

thereby establishing synthesis quality and fidelity of the in situ synthesized peptide array, wherein a correlation value of less than a threshold level indicates a quality of an immunosignature assay using the in situ synthesized peptide array.

2. The method of claim 1 , wherein the correlation value is obtained by Kolmogorov-Smirnov test, Pearson Correlation or Pearson Squared.

3. The method of claim 1 , wherein the threshold level is defined as a percentage of the correlation coefficient between assays.

4. The method of claim 1 , wherein the peptide array is a random or partially random peptide array.

5. The method of claim 1 , wherein the first binding pattern is obtained from a subset of peptides on the peptide array, and the second binding pattern is obtained from a corresponding subset of peptides on the peptide reference array.

6. The method of claim 1 , wherein the first binding pattern is obtained from binding with the first sample, the second binding pattern is obtained from binding with a second sample, wherein the first sample and the second sample are from a same species.

7. The method of claim 6 , wherein the first sample and the second sample are not from the same subject.

8. The method of claim 6 , wherein the species is human being.

9. The method of claim 6 , wherein the first sample and the second sample are acquired from a blood sample.

10. The method of claim 1 , wherein the biological sample is a blood sample, a serum sample, a plasma sample, a urine sample, a sputum sample, a mucosal sample, a peritoneal fluid sample, a tissue sample, an exudate or an effusion.

11. A method for determining quality and fidelity of an in situ synthesized peptide array configured for use in an immunosignature assay, comprising:

providing an array of peptides, wherein the peptides are synthesized in situ in a stepwise manner on the surface of an array, wherein the in situ synthesized peptide array comprises at least 100 compounds;

incubating a biological sample on the peptide array;

obtaining a first binding pattern of the biological sample binding to the in situ synthesized peptide array;

obtaining a second binding pattern of an in situ synthesized reference peptide array;

comparing the first binding pattern with the second binding pattern and calculating a correlation value, wherein the comparing comprises a direct peptide-by-peptide comparison between the first and the second binding patterns to evaluate a number of peptides expressing different patterns and a comparison between a binding profile of the first binding pattern and a binding profile of the second binding pattern to evaluate a level of similarity between the binding profiles, wherein each of the binding profiles comprises a distribution of signals measured from a population of at least 2 arrayed compounds; and

thereby establishing synthesis quality and fidelity of the in situ synthesized peptide array, wherein a correlation value of less than a threshold level indicates a quality of an immunosignature assay using the in situ synthesized peptide array.

12. The method of claim 11 , wherein the correlation value is obtained by Kolmogorov-Smirnov test, Pearson Correlation or Pearson Squared.

13. The method of claim 11 , wherein the threshold level is defined as a percentage of the correlation coefficient between assays.

14. The method of claim 11 , wherein the peptide array is a random or partially random peptide array.

15. The method of claim 11 , wherein the first binding pattern is obtained from a subset of peptides on the peptide array, and the second binding pattern is obtained from a corresponding subset of peptides on the peptide reference array.

16. The method of claim 11 , wherein the first binding pattern is obtained from binding with the first sample, the second binding pattern is obtained from binding with a second sample, wherein the first sample and the second sample are from a same species.

17. The method of claim 16 , wherein the first sample and the second sample are not from the same subject.

18. The method of claim 16 , wherein the species is human being.

19. The method of claim 16 , wherein the first sample and the second sample are acquired from a blood sample.

20. The method of claim 1 , wherein the biological sample is a blood sample, a serum sample, a plasma sample, a urine sample, a sputum sample, a mucosal sample, a peritoneal fluid sample, a tissue sample, an exudate or an effusion.

Assignments (3)
CONFIRMATORY LICENSE Recorded Feb 12, 2020
From: ARIZONA STATE UNIVERSITY
To: DEFENSE THREAT REDUCTION AGENCY, US DOD
Reel/Frame 051907/0435 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 21, 2018
From: WOODBURY, NEAL; JOHNSTON, STEPHEN; STAFFORD, PHILLIP
To: ARIZONA BOARD OF REGENTS, A BODY CORPORATE OF THE STATE OF ARIZONA, ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY
Reel/Frame 046170/0970 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 21, 2018
From: ARIZONA BOARD OF REGENTS, A BODY CORPORATE OF THE STATE OF ARIZONA, ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY., A ARIZONA CORPORATION
To: ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY
Reel/Frame 046171/0198 →
Continuity (3)
Continuation 14773750
Provisional Application 61799494 · Mar 15, 2013
Related Publication 20180275136A1 · Sep 27, 2018
Cited By (1)
US 12,350,672