High affinity recombinant sea lamprey antibodies selected by a Yeast Surface Display platform
The present invention relates to a Yeast Surface Display (YSD) vector for expression of VLR proteins by yeast, wherein the vector includes nucleotide sequences encoding segments of yeast flocculation proteins Flo1p, such as the leader and C-terminal segments, a homologous recombinant cassette and a geneticin/kanamycin resistance gene. The vector can be used for expression of VLR that may be effective in diagnostic applications (e.g., protein chip, immunohistochemistry, flow cytometry), immunoaffinity purification, and for engineering novel fusion proteins.
1. A Yeast Surface Display (YSD) vector for expression of a variable lymphocyte receptor (VLR) protein positioned on the surface of a yeast cell comprising:
a nucleotide sequence encoding for the VLR protein, wherein the VLR protein was formed in response to an antigen and having affinity for the antigen;
nucleotide sequences encoding a leader and C-terminal segment of yeast flocculation protein Flo1p, wherein the nucleotide sequence encoding for the VLR protein is positioned therebetween; and
a homologous recombination cassette consisting of two same number of base-pair direct repeats separated by a linker wherein the linker comprises a restriction site for plasmid linearization.
2. The YSD of claim 1 , further comprising the inclusion of a geneticin/kanamycin resistance gene.
3. The YSD of claim 1 , wherein the two base-pair direct repeats consists of 49 base-pairs.
4. The YSD of claim 1 , wherein the nucleotide sequence encoding the leader and C-terminal of yeast flocculation protein Flo1p is SEQ ID NOs.: 6 and 7, respectively.
5. The YSD of claim 1 , wherein the yeast is a strain of Saccharomyce cerevisiae.
6. A method for providing a high-throughput platform for selection of recombinant antigen-binding VLR proteins, the system comprising:
a) providing yeast strains of Saccharomyce cerevisiae and
b) transfecting the yeast with the YSD vector of claim 1 ; and
c) culturing the yeast for expression and displaying of the VLR proteins on the surface of the yeast.
7. The method of claim 6 , wherein the culturing of the yeast further comprising the use of a growth medium that includes yeast peptone and sugar.
8. The method of claim 6 , further comprising the inclusion of a geneticin/kanamycin resistance gene.
9. The method of claim 6 , wherein the nucleotide sequence encoding the leader and C-terminal of yeast flocculation protein Flo1p is SEQ ID NOs.: 6 and 7, respectively.
10. A method of producing VLR proteins having high affinity for an antigen of choice, the method comprising:
a) immunizing a Lamprey with the antigen and collecting plasma containing the VLR proteins formed in response to the antigen;
b) determining nucleotide sequence encoding such VLR proteins;
c) preparing the YSD vector of claim 1 :
d) transfecting a yeast strain;
e) culturing the yeast for expression and displaying of the VLR proteins on the surface of the yeast; and
f) measuring the binding affinity.
11. The method of claim 10 , wherein the culturing of the yeast further comprising the use of a growth medium that includes yeast peptone and sugar.
12. The method of claim 10 , further comprising the inclusion of a geneticin/kanamycin resistance gene.
13. The method of claim 10 , wherein the nucleotide sequence encoding the leader and C-terminal of yeast flocculation protein Flo1p is SEQ ID NOs.: 6 and 7, respectively.
14. The method of claim 10 , further comprising subjecting the nucleotide sequence encoding for the VLR protein to mutagenesis and repeat steps (c) to (f) until affinity increases for antigen of choice.
15. The YSD vector of claim 1 , wherein the nucleotide sequence encoding the VLR protein comprises nucleotide sequence encoding for the stalk C-terminal of the VLP protein.