IP Library Granted Patent US 8,685,392
Granted Patent B2
US 8,685,392 · App. 13/500,670 · Granted Apr 1, 2014

Patent

Inventors: Eva J. Helmerhorst (Chestnut Hill, MA); Frank G. Oppenheim (Chestnut Hill, MA)
Assignee: Trustees of Boston University
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Quick Facts
Patent No.
US 8,685,392
App. No.
13/500,670
Granted
Apr 1, 2014
Kind
B2
Abstract

The invention relates to glutamine endopeptidase enzymes from Rothia spp. bacteria that are naturally associated with the oral cavity, formulations comprising the glutamine endopeptidase enzymes and the use thereof for the treatment, prevention of allergic reaction and diagnosis of gluten allergy related diseases such as Celiac Sprue, gluten allergy and/or dermatitis herpetiformis.

Claims (15)

1. A gluten-containing foodstuff comprising a formulation comprising an isolated glutamine endopeptidase enzyme that cleaves a peptide bond after a QPF and a PFP motif in glutens.

2. The formulation of claim 1 , wherein the isolated enzyme has an apparent molecular weight of about 70-75 kDa as determined by gliadin zymograms or by sodium dodecyl sulfate polyacrylamide gel electrophoresis.

3. The formulation of claim 2 , wherein the isolated enzyme has a functional pH range of 3-10 as determined by detectable Z-YPQ-pNA cleaving activity within a 72 hour digestion period and a functional pH range of 7-10 as determined by substantially complete Z-YPQ-pNA cleavage within a 1 hour digestion period.

4. The formulation of claim 3 , wherein the isolated enzyme is 100% inhibited by 1 mM of PMSF.

5. The formulation of claim 4 , wherein the isolated enzyme is derived from a Rothia species bacteria, wherein the Rothia species bacteria is selected from the group consisting of Rothia mucilaginosa ot 681 (strain WSA-2B), Rothia mucilaginosa ATCC 25296 and Rothia species ot 188 (strain WSA-8).

6. The formulation of claim 5 , wherein the isolated enzyme is stable in acid conditions.

7. The formulation of claim 6 , wherein the isolated enzyme is lyophilized.

8. The formulation of claim 7 , wherein the isolated enzyme has an amino acid sequence that show at least 60% similarity to SEQ. ID. NO: 1.

9. The formulation of claim 7 , wherein the isolated enzyme comprises SEQ. ID. NO: 1.

10. The formulation of claim 7 , wherein the isolated enzyme consists essentially of SEQ. ID. NO: 1.

11. The formulation of claim 7 , wherein the isolated enzyme is SEQ. ID. NO: 1.

12. The formulation of claim 11 further comprising a prolyl endopeptidase.

13. A method of digesting gluten, the method comprising contacting a gluten-containing foodstuff with an effective dose of a formulation comprising an isolated glutamine endopeptidase enzyme that cleaves a peptide bond after a QPF and a PFP motif in glutens.

14. The method of claim 13 , wherein the contacting is performed in vitro prior to consumption of the gluten-containing food stuff.

15. The method of claim 13 , wherein the contacting is performed in vivo concurrent with or after consumption of the gluten-containing food stuff.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 1, 2013
From: BOSTON UNIVERSITY MEDICAL CAMPUS
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 031532/0276 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 29, 2012
From: HELMERHORST, EVA J.; OPPENHEIM, FRANK G.
To: TRUSTEES OF BOSTON UNIVERSITY
Reel/Frame 028278/0081 →
Continuity (2)
Provisional Application 61249343 · Oct 7, 2009
Related Publication 20120230976A1 · Sep 13, 2012