Frame-shifting PCR for germline immunoglobulin genes retrieval and antibody engineering
A method for preparing an antigen-specific antibody by constructing a library of phage-displayed single chain variable fragment of an antibody with a novel frame-shifting PCR is disclosed. Also disclosed is a method for preparing a clone for producing an antigen-specific antibody.
1. A method for preparing single-chain variable fragments encoding an antigen-specific antibody, comprising the steps of:
a) extracting genomic DNAs of lymphocytes from a non-immunized mammal or a mammal immunized with a specific antigen;
b) recovering variable regions of immunoglobulin heavy and light chains from the genomic DNAs;
c) amplifying the variable regions using PCR with a forward primer and a set of different reverse primers designed for the variable regions, wherein the reverse primers are represented by gAcDgTgASHRDRgTBccTKSRccccANNNNNN for V H or YYTKgTSccHBcDccgAAYgTNNNNNN for V L-κ , in which N is A, c, T or g, R is A or g, Y is c or T, M is A or c, K is T or g, S is c or g, H is A, T or c, B is T, c or g, and D is A, T or g;
d) introducing both an adaptor and a linker to the variable regions obtained in step c); and
e) linking the variable regions obtained in step d) by an overlap-extensive PCR to obtain single-chain variable fragments.
2. The method of claim 1 , wherein the step b) is performed by a semi-nested PCR.
3. The method of claim 2 , wherein the mammal is a mouse.
4. The method of claim 2 , wherein the specific antigen is 4-ethoxymethylene-2-phenyl-2-oxazolin-5-one conjugated to chicken serum albumin.
5. The method of claim 1 , wherein the forward primer is gAggTgMWgcTKVWg for V H , in which M is A or c, K is T or g, W is A or T, and V is A, c or g.
6. The method of claim 1 , wherein the forward primer is gAHRTYgTKMTSAcMcARWcTMcA for V L-κ , in which R is A or g, Y is c or T, M is A or c, K is T or g, S is c or g, and H is A, T or c.
7. The method of claim 1 , wherein the PCR for both VH and VL- κ is performed with a condition as follows:
preheating at 94° C. for 2 min, then followed with 25 cycles of denaturation at 94° C. for 30 sec, annealing at 20° C. for 2 min, extension at ramping up w/speed 0.1° C./sec, and then storage at 4° C.
8. The method of claim 1 , wherein the lymphocytes are splenoctic CD + 19 cells.
9. A method for preparing an antigen-specific antibody comprising:
a) extracting lymphocytic genomic DNAs from a non-immunized mammal or a mammal immunized with a specific antigen;
b) recovering variable regions of immunoglobulin heavy and light chains from the genomic DNAs;
c) amplifying the variable regions using PCR with a forward primer and a set of different reverse primers designed for the variable regions, wherein the reverse primers are represented by gAcDgTgASHRDRgTBccTKSRccccANNNNNN for V H or YYTKgTSccHBcDccgAAYgTNNNNNN for V L-κ , in which N is A, c, T or g, R is A or g, Y is c or T, M is A or c, K is T or g, S is c or g, H is A, T or c, B is T, c or g, and D is A, T or g;
d) introducing both an adaptor and a linker to the variable regions obtained in step c);
e) linking the variable regions obtained in step d) by an overlap-extensive PCR to construct single-chain variable fragments; and
f) introducing the single-chain variable fragments into a host cell and expressing the cell.
10. The method of claim 9 , wherein the antigen-specific antibody is a monoclonal antibody.
11. The method of claim 10 , wherein the monoclonal antibody is a monoclonal antibody of single-chain variable fragments.
12. A method for retrieving either V L-κ or V H genes from a genomic DNA comprising the steps of:
a) extracting lymphocytic genomic DNAs from a mammal;
b) recovering variable regions of immunoglobulin heavy and light chains from the genomic DNAs using a semi-nested PCR; and
c) amplifying the variable regions using PCR to produce V L-κ or V H genes of variable lengths or sequences, with a set of different reverse primers which are represented by gAcDgTgASHRDRgTBccTKSRccccANNNNNN for V H or YYTKgTSccHBcDccgAAYgTNNNNNN for V L-κ , in which N is A, c, T or g, R is A or g, Y is c or T, M is A or c, K is T or g, S is c or g, H is A, T or c, B is T, c or g, and D is A, T or g.
13. The method of claim 12 , wherein the mammal is a non-immunized one or immunized with a specific antigen.
14. The method of claim 13 , wherein the mammal is a mouse and the specific antigen is 4-ethoxymethylene-2-phenyl-2-oxazolin-5-one conjugated to chicken serum albumin.
15. A method for constructing a library of recombinant nucleotide sequences encoding V L-κ or V H genes from a genomic DNA comprising the steps of:
a) extracting lymphocytic genomic DNAs from a mammal;
b) recovering variable regions of immunoglobulin heavy and light chains from the genomic DNAs using a semi-nested PCR;
c) amplifying the variable regions using PCR to produce V L-κ or V H genes of variable lengths or sequences, with a set of different reverse primers which are represented by gAcDgTgASHRDRgTBccTKSRccccANNNNNN for V H or YYTKgTSccHBcDccgAAYgTNNNNNN for V L-κ , in which N is A, c, T or g, R is A or g, Y is c or T, M is A or c, K is T or g, S is c or g, H is A, T or c, B is T, c or g, and D is A, T or g; and
d) cloning the V L-κ or V H genes into a vector.
16. The method of claim 15 , wherein the mammal is a non-immunized one or immunized with a specific antigen.
17. The method of claim 16 , wherein the mammal is mouse and the specific antigen is 4-ethoxymethylene-2-phenyl-2-oxazolin-5-one conjugated to chicken serum albumin.
18. The method of claim 15 , wherein the vector is a TOPO TA vector.
19. The method of claim 17 , wherein the vector is a TOPO TA vector.