Method for detecting and removing endotoxin
The present invention relates to bacteriophage tail proteins and the derivatives and fragments thereof that are capable of binding endotoxins in the absence of bivalent positive ions, especially Ca 2+ or Mg 2+ . Further, the present invention relates to methods for depleting endotoxins from solutions and samples using the bacteriophage tail proteins according to the present invention and to a detection method for endotoxins.
1. A method for removing an endotoxin from a sample, comprising the steps:
a) contacting a bacteriophage tail protein with a sample, wherein the bacteriophage tail protein binds said endotoxin independent of bivalent positive ion concentrations; and subsequently
b) separating the endotoxin-bacteriophage tail protein complex from the sample,
wherein the bacteriophage tail protein is selected from the group consisting of SEQ ID NOs: 2, 4, 6, 8, 10, 12 and 14.
2. The method according to claim 1 , wherein steps a) and b) comprise column chromatography.
3. The method of claim 1 , wherein bacteriophage tail proteins are directedly immobilized to a solid carrier.
4. The method according to claim 3 , wherein the solid carrier is cellulose, filtration media, glass particles, magnetic particles, centrifugation or sedimentation substances or packing material for chromatography columns.
5. The method of claim 3 , wherein the bacteriophage tail protein is immobilized to the solid carrier by coupling groups.
6. The method according to claim 3 , wherein the bacteriophage tail protein is covalently immobilized to the solid carrier by chemical bonds.
7. The method according to claim 1 , wherein the bacteriophage tail protein comprises a Strep-tag or a His-tag.
8. The method according to claim 1 , wherein the bacteriophage tail protein is a short bacteriophage tail protein.
9. The method according to claim 1 , wherein the bacteriophage tail protein comes from the Myoviridae family.
10. The method according to claim 1 , wherein the bacteriophage tail protein is selected from the group consisting of pseudo-T-even, schizo-T-even and T-even phage.
11. The method according to claim 1 , wherein the bacteriophage tail protein binds 2-keto-3-deoxyoctonic acid in the core region of the endotoxin.
12. The method according to claim 1 , wherein the concentration of free unbound bivalent positive ions is less than 0.1 μM.
13. The method according to claim 1 , wherein the bivalent positive ions are Ca 2+ and/or Mg 2+ .
14. An isolated polypeptide comprising SEQ ID NO: 2, 4, 6, 8, 10, 12 or 14.
15. A method for the detection of endotoxin comprising the steps:
a) contacting an endotoxin-containing sample with a surface; subsequently
b) incubating a bacteriophage tail protein with an endotoxin immobilized to the surface, wherein the bacteriophage tail protein binds endotoxin independent of bivalent positive ion concentration; subsequently
c) removing the unbound bacteriophage tail protein; and subsequently
d) detecting the unbound bacteriophage tail protein of step c),
wherein the bacteriophage tail protein is selected from the group consisting of SEQ ID NOs: 2, 4, 6, 8, 10, 12 and 14.
16. The method according to claim 15 , further comprising the additional step after step a) and before step b) of removing the sample from the surface.
17. The method according to claim 15 , wherein the surface is coated with an endotoxin-binding ligand by adsorption or covalent coupling.
18. The method according to claim 17 , wherein the endotoxin binding ligand is a bacteriophage tail protein that binds endotoxin independent of the bivalent positive ion concentration.
19. A method for the detection of endotoxin comprising the steps:
a) contacting an endotoxin-containing sample to a surface immobilized with a first bacteriophage tail protein that binds endotoxin independent of bivalent positive ion concentration; subsequently
b) removing the sample from the surface; subsequently
c) incubating of a second bacteriophage tail with the endotoxin bound to the first bacteriophage tail protein, wherein the second bacteriophage tail protein binds endotoxin only in the presence of bivalent positive ions; subsequently removing unbound second bacteriophage tail protein; and subsequently
d) detecting the second bacteriophage tail protein bound to endotoxin,
wherein the bacteriophage tail protein is selected from the group consisting of SEQ ID NOs: 2, 4, 6, 8, 10, 12 and 14.
20. A method for the detection of endotoxin comprising the steps:
a) contacting an endotoxin-containing sample to a surface immobilized with a bacteriophage tail protein that binds endotoxin independent of bivalent positive ion concentration; subsequently
b) removing the sample from the surface; and subsequently
c) detecting the endotoxin bound in step a),
wherein the bacteriophage tail protein is selected from the group consisting of SEQ ID NOs: 2, 4, 6, 8, 10, 12 and 14.
21. The method according to claim 15 , wherein detecting is carried out by spectroscopic methods, ELISA, chemical or enzymatic detection reaction of endotoxin or separated endotoxin components or by capacity measurement.
22. A method for the detection of endotoxin comprising the steps:
a) mixing a sample with an endotoxin coupled to a marker; subsequently
b) applying the mixture of step a) to a surface with an immobilized bacteriophage tail protein, wherein the bacteriophage tail protein binds endotoxin independent of bivalent positive ion concentration; subsequently
c) removing the mixture from the surface; subsequently
d) washing the surface; and subsequently
e) detecting labeled endotoxin on the surface and/or free labeled endotoxin of the pooled samples after steps c) and d),
wherein the bacteriophage tail protein is selected from the group consisting of SEQ ID NOs: 2, 4, 6, 8, 10, 12 and 14.