Method for recombinant production of horseshoe crab Factor C protein in protozoa
The present invention provides a novel method for the recombinant production of Factor C protein from horseshoe crab using a parasitic protozoan expressing the Factor C protein. In particular, the present invention provides a parasitic protozoan host cell harbouring a polynucleotide encoding horseshoe crab Factor C protein, and a method for producing Factor C protein comprising culturing said parasitic protozoan host cell under conditions such that the cells express the horseshoe crab Factor C protein. Furthermore, the present invention provides recombinant Factor C protein produced by the novel method and its use in the detection and/or removal of endotoxin.
1. A method for detecting endotoxin in a sample suspected of containing endotoxin, the method comprising
a) obtaining a recombinant horseshoe crab Factor C prepared by culturing a parasitic protozoan comprising a polynucleotide encoding horseshoe crab Factor C protein, said protozoan expressing a two-chain zymogen form of horseshoe crab Factor C protein having a molecular weight of about 102 kDa as determined by SDS-PAGE under non-reducing conditions, said zymogen being rendered enzymatically active upon contacting lipopolysaccharide and recovering the recombinant Factor C; and
b) contacting the sample to be assayed for the presence of endotoxin with the recombinant horseshoe crab Factor C by measuring serine protease activity of the recombinant Factor C.
2. The method of claim 1 , wherein the parasitic protozoan is a member of the order Trypanosomatida.
3. The method of claim 2 , wherein the parasitic protozoan is a member of the genus Leishmania.
4. The method of claim 3 , wherein the parasitic protozoan is Leishmania tarentolae.
5. The method of claim 1 , wherein said polynucleotide encodes Factor C protein from Limulus polyphemus, Carcinoscorpius rotundicauda, Tachypleus tridentatus , or Tachypleus gigas.
6. The method of claim 1 , wherein enzymatic activity of the recombinant Factor C is measured through the use of a chromogenic or fluorogenic substrate followed by chromogenic or fluorogenic detection.
7. The method of claim 6 , wherein the substrate is a chromogenic peptidyl-pNA substrate or fluorogenic peptidyl-AMC, peptidyl-AFC, or peptidyl-MCA substrates.
8. The method of claim 7 , wherein the substrate is N-t-Boc-VPR-MCA, N-t-BocVPR-AMC, Mu-VPR-AFC or Boc-VPR-pNA.
9. The method of claim 1 , wherein the expressed Factor C protein is accumulated in the cell culture medium.
10. The method of claim 1 , wherein said polynucleotide encodes Factor C protein having the amino acid sequence of SEQ ID NO: 4.