IP Library › Granted Patent US 9,782,461
Granted Patent B2
US 9,782,461 · App. 14/894,415 · Granted Oct 10, 2017

Human coagulation factor light chain protein and use of the same

Inventors: Xu Song (Sichuan, CN); Ling Li (Sichuan, CN); Jinwu Chen (Sichuan, CN); Dongsheng Liao (Sichuan, CN); Dengjiao Ma (Sichuan, CN)
Assignee: Chengdu Sourcebio Limited-Liability Company
A61K38/4846C07K14/745A61K38/00C12Y304/21006C12Y304/21021C12Y304/21022
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 9,782,461
App. No.
14/894,415
Granted
Oct 10, 2017
Kind
B2
Abstract

In the invention, the minimum inhibitory concentrations of human coagulation factor light-chain proteins against different Gram-negative bacteria are detected with the in vitro antibacterial activity and the inhibiting effect of the human coagulation factor light-chain proteins against different Gram-negative bacteria is detected with the in vivo antibacterial activity. It has been shown that human coagulation factor light-chain proteins have an obvious inhibitory effect on the Gram-negative bacteria, so as to develop a novel class of medicaments for treating Gram-negative bacteria infection. It has been demonstrated by mass spectrometry and silver staining that human coagulation factor light-chain proteins have the effect on hydrolyzing and eliminating the endotoxin, which facilitates the development of a novel class of medicaments for treating endotoxemia. The human coagulation factor light-chain proteins are light chain proteins of human coagulation factors VII, IX, and X, as well as a protein having homology of more than 50% thereof.

Claims (14)

1. A method for treating a disease caused by Gram-negative bacteria infection, said method comprises administering an effective amount of protein encoded by a human coagulation factor light-chain gene or a pharmaceutical composition thereof to a subject.

2. The method of claim 1 , wherein the disease caused by Gram-negative bacteria infection is endotoxemia.

3. The method of claim 1 , wherein the protein encoded by a human coagulation factor light-chain gene comprises amino acid sequence SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3 or combinations thereof.

4. The method of claim 2 , wherein the protein encoded by a human coagulation factor light-chain gene comprises amino acid sequence SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3 or any combination thereof.

5. The method of claim 1 , wherein the Gram-negative bacteria is one or more of Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumonia, Enterobacter cloacae, Aeromonas hydrophila, Citrobacter diversus, Moraxella catarrhalis, Proteus mirabilis, Proteus vulgaris and Serratia marcescens.

6. The method of claim 2 , wherein the Gram-negative bacteria is one or more of Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumonia, Enterobacter cloacae, Aeromonas hydrophila, Citrobacter diversus, Moraxella catarrhalis, Proteus mirabilis, Proteus vulgaris and Serratia marcescens.

7. The method of claim 3 , wherein the Gram-negative bacteria is one or more of Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumonia, Enterobacter cloacae, Aeromonas hydrophila, Citrobacter diversus, Moraxella catarrhalis, Proteus mirabilis, Proteus vulgaris and Serratia marcescens.

8. The method of claim 4 , wherein the Gram-negative bacteria is one or more of Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumonia, Enterobacter cloacae, Aeromonas hydrophila, Citrobacter diversus, Moraxella catarrhalis, Proteus mirabilis, Proteus vulgaris and Serratia marcescens.

9. A method for hydrolyzing a lipopolysaccharide, said method comprising contacting a lipopolysaccharide with an effective amount of protein encoded by a human coagulation factor light-chain gene or a pharmaceutical composition thereof to hydrolyze the lipopolysaccharide.

10. The method of claim 9 , wherein the lipopolysaccharide is a lipopolysaccharide of a Gram-negative bacteria.

11. The method of claim 10 , wherein the Gram-negative bacteria is one or more of Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumonia, Enterobacter cloacae, Aeromonas hydrophila, Citrobacter diversus, Moraxella catarrhalis, Proteus mirabilis, Proteus vulgaris and Serratia marcescens.

12. The method of claim 9 , wherein the protein encoded by a human coagulation factor light-chain gene comprises amino acid sequence SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3 or any combination thereof.

13. The method of claim 10 , wherein the protein encoded by a human coagulation factor light-chain gene comprises amino acid sequence SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3 or any combination thereof.

14. The method of claim 11 , wherein the protein encoded by a human coagulation factor light-chain gene comprises amino acid sequence SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3 or any combination thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2016
From: SONG, XU; LI, LING; CHEN, JINWU; LIAO, DONGSHENG; MA, DENGJIAO
To: SICHUAN UNIVERSITY
Reel/Frame 040362/0008 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2016
From: SICHUAN UNIVERSITY
To: CHENGDU SOURCEBIO LIMITED-LIABILITY COMPANY
Reel/Frame 040362/0087 →
Priority Claims (1)
CN 2013 1 0206823 · May 29, 2013 · national
Continuity (1)
Related Publication 20160106818A1 · Apr 21, 2016