Humanized antibodies to ganglioside GM.sub.2

FIELD OF THE INVENTION
The present invention relates to humanized antibodies reacting with the ganglioside GM.sub.2. The humanized antibodies do not cause production of anti-mouse immunoglobulins in the patient's body as compared with mouse monoclonal antibodies, hence the incidence of adverse effects possibly caused by them is much lower, their blood half-lives are longer and, further, their anti-tumor effector effect is greater. Therefore, the humanized antibodies are expected to produce improved therapeutic effects as compared with mouse monoclonal antibodies.
BACKGROUND OF THE INVENTION
When administered to humans, mouse antibodies are generally recognized as foreign matters, inducing production of anti-mouse immunoglobulin antibodies in the human body. It is known that the former antibodies react with the latter antibodies to produce adverse effects �J. Clin. Oncol., 2, 881 (1984); Blood, 65, 1349 (1985); J. Natl. Cancer Inst., 80, 932 (1988); Proc. Natl. Acad. Sci. U.S.A., 82, 1242 (1985)! and that the mouse antibodies undergo rapid clearance �J. Nucl. Med., 26, 1011 (1985); Blood, 65, 1349 (1985); J. Natl. Cancer Inst., 80, 937 (1988)!, thus showing only a reduced efficacy �J. Immunol., 135, 1530 (1985); Cancer Res., 46, 6489 (1986)!. Attempts have been made to solve these problems by deriving, from mouse monoclonal antibodies, chimeric human antibodies or CDR (complementarity determining region)-transplanted antibodies (reshaped antibodies) using gene engineering technique. In a human chimeric antibody, the variable regions thereof are of mouse origin and the constant regions thereof are of human origin �Proc. Natl. Acad. Sci. U.S.A., 81, 6851 (1984)! and it is reported that when administered to humans, said antibody causes litte human anti-mouse immunoglobulin antibody production, its blood half-life being 6-fold longer �Proc. Natl. Acad. Sci. U.S.A., 86, 4220 (1989)!. The CDR-transplanted antibodies are antibodies resulting from replacement of the CDRs in a human antibody alone with the CDRs from an animal other than the human �Nature, 321, 522 (1986)! and, in an experiment with monkeys, such antibodies showed reduced immunogenicity and 4- to 5-fold higher serum half-lives as compared with mouse antibodies �J. Immunol., 147, 1352 (1991)!.
As regards the cytocidal activity of antibodies, it is reported that the Fc region of a human antibody is more potent in activating human complement and human effector cells than the Fc region of a mouse antibody. Thus, for instance, a chimeric antibody derived from a mouse monoclonal antibody to the ganglioside GD.sub.2 and containing a human antibody Fc region enhances the human effector cell-mediated antitumor effect �J. Immunol., 144, 1382 (1990)!. Similar results are reported for CDR-transplanted antibodies �Nature, 332, 323 (1988)!. Such results indicate that, for clinical use, humanized monoclonal antibodies are preferred to mouse monoclonal antibodies.
The antibody classes include IgA, IgM, IgG, IgD and IgE and, in mice, the class IgG includes four subclasses, namely IgG.sub.1, IgG.sub.2 a, IgG.sub.2 b and IgG.sub.3 (in humans, IgG.sub.1, IgG.sub.2, IgG.sub.3 and IgG.sub.4). When antigens are administered to animals, the antibodies produced mostly belong to the classes IgM or IgG. IgG molecules have a molecular weight of about 160,000 daltons and a dimeric structure and are relatively easy to handle. IgM molecules are large with a molecular weight of about 900,000 daltons and occur in the form of a complicated pentameric structure coupled with the joining (J) chain, hence they have the following drawbacks: they are difficult to purify; they tend to agglutinate, hence are difficult to store; they are readily inactivated by partial decomposition in the presence of a protease, hence it is difficult to prepare Fab fragments; and they lose their binding activity in many instances upon chemical modification, for example chemical binding of an anticancer agent or a toxin �J. W. Goding: Monoclonal Antibodies: Principles and Practice, Academic Press, 1986!. As to which are superior in therapeutic effect against cancer, IgG class monoclonal antibodies or IgM class monoclonal antibodies, reference may be made to a detailed study made by Bernstein et al. using an IgG class monoclonal antibody and an IgM class monoclonal antibody to the lymphocyte Thy-1 antigen �Monoclonal Antibodies, edited by R. H. Kennet, T. J. Mckearn and K. B. Bechtol, Plenum Press, 1980, p. 275!. According to the reference, an IgG class monoclonal antibody and an IgM class monoclonal antibody comparable in terms of reactivity to Thy-1 antigen-positive lymphocytes, were compared in terms of antitumor effect. While the IgM monoclonal antibody was superior in in vitro complement-dependent antitumor effect, the IgG class monoclonal antibody showed a significant antitumor effect in in vivo antitumor effect in cancer-bearing mice, with no antitumor effect being observed with the IgM class monoclonal antibody. It was further revealed that, as compared with the IgG class monoclonal antibody, the IgM class monoclonal antibody showed a very short half-life in the blood after administration, in an isotope-labeled form, to mice. These results indicate that the monoclonal antibodies to be used clinically in humans should preferably be of the IgG class.
Gangliosides, a class of glycolipids, are constituents of animal cell membranes. These molecules are composed of a carbohydrate chain, which constitutes a hydrophilic side chain, and sphingosine and a fatty acid, which constitute hydrophobic side chains. It is known that the ganglioside species expressed and the amount thereof differ between cell species, organ species, and animal species, among others. Furthermore, it has been reported that the ganglioside expressed changed quantitatively and qualitatively during the process of cancer development �Cancer Res., 45, 2405 (1985)!. For example, expression of the gangliosides GD.sub.2, GD.sub.3 and GM.sub.2 has been reported in neuroblastoma, lung small cell carcinoma, and melanoma, which are highly malignant neural ectodermal tumors �J. Exp. Med., 155, 1133 (1982); J. Biol. Chem., 257, 12752 (1982); Cancer Res., 47, 225 (1987); ibid., 47, 1098 (1987); ibid., 45, 2642 (1985); Proc. Natl. Acad. Sci. U.S.A., 80, 5392 (1983)!.
GM.sub.2, one of the gangliosides that are sialic acid residue containing glycolipids, occurs only in trace amounts in normal cells but is found in increased amounts in cancer cells in lung small cell carcinoma, melanoma, neuroblastoma, etc. Monoclonal antibodies to GM.sub.2 are considered to be useful in the treatment of such cancers �Lancet, 4, 786 (1989)!. However, those monoclonal antibodies to GM.sub.2 that have so far been reported are of the human IgM class or of the rat IgM, mouse IgM or mouse IgG class �Cancer Res., 46, 4116 (1986); Proc. Natl. Acad. Sci. U.S.A., 79, 7629 (1982); Cancer Res., 48, 6154 (1988); J. Biol. Chem., 264, 12122 (1989)!.
Anti-ganglioside GM.sub.2 monoclonal antibodies, if produced in the form of humanized antibodies, for example chimeric human antibodies or CDR-transplanted antibodies, which are not expected to induce anti-mouse immunoglobulin antibody production in the patient's body, produce reduced adverse effects and show a prolonged blood half-life and an enhanced antitumor effector effect. These antibodies are thus expected to be superior in therapeutic effect to the corresponding mouse monoclonal antibodies.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide humanized antibodies to the ganglioside GM.sub.2 (hereinafter, "humanized anti-GM.sub.2 antibodies") which are useful in the treatment of cancers of neural ectodermal origin, among others.
The present inventors prepared the antibody heavy chain (hereinafter, "H chain") variable region (hereinafter "V.sub.H ") cDNA and light chain (hereinafter, "L chain") variable region (hereinafter, "V.sub.L ") cDNAs from mRNAs isolated from the hybridomas KM750 and KM796, described in EP-A-0 508 472. These hybridomas produce IgG.sub.3 class mouse monoclonal antibodies to the ganglioside GM.sub.2. V.sub.H and V.sub.L cDNAs were also prepared from mRNAs isolated from the hybridoma KM603, which produces an IgM class rat monoclonal antibody to the ganglioside GM.sub.2. Chimeric human antibody expression vectors were constructed by inserting the cDNA into an expression vector containing human antibody H chain constant region (hereinafter, "C.sub.H ") or human antibody L chain constant region (hereinafter, "C.sub.L ") encoding sequences. Such vectors were then introduced into animal cells to effect the production of anti-ganglioside GM.sub.2 chimeric human antibodies. Among the chimeric antibodies produced, the anti-ganglioside GM.sub.2 chimeric human antibody, KM966, was found to react with the ganglioside GM.sub.2 and show cytocidal activity. The H chain variable region of KM966 contains an amino acid sequence segment as defined by SEQ ID NO:91 and includes the 1st to 120th amino acids of that sequence and the L chain variable region of KM966 contains an amino acid sequence segment as defined by SEQ ID NO:92 and includes the 1st to 107th amino acids of said sequence. The present invention is based, at least in part, on these findings.
The present invention thus relates to a humanized antibody reacting with the ganglioside GM.sub.2.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 illustrates plasmids, pKM796H1 and pKM796L1.
FIG. 2 illustrates plasmids, pKM750H1 and pKM750L1.
FIG. 3 illustrates plasmids, pKM603H1 and pKM603L1.
FIG. 4 shows a construction scheme for a plasmid, pAGE147.
FIG. 5 shows a construction scheme for a plasmid, pAGE148.
FIG. 6 shows a construction scheme for plasmids, pChi796HM1 and pChi750HM1.
FIG. 7 shows a construction scheme for plasmids, pChi796HMS1 and pChi750HMS1.
FIG. 8 shows a construction scheme for plasmids, pChi796LI1 and pChi750LI1.
FIG. 9 shows a construction scheme for plasmids, pChi796LM1 and pChi750LM1.
FIG. 10 shows a construction scheme for plasmids, pChi796LMS1 and pChi750LMS1.
FIG. 11 shows a construction scheme for plasmids, pChi796H107 and pChi750H107.
FIG. 12 shows a construction scheme for plasmids, pChi796HL1 and pChi750HL1.
FIG. 13 shows a construction scheme for a plasmid, pChi603HM1.
FIG. 14 shows a construction scheme for a plasmid, pChi603HMS1.
FIG. 15 shows a construction scheme for a plasmid, pChi603LI1.
FIG. 16 shows a construction scheme for a plasmid, pChi603LM1.
FIG. 17 shows a construction scheme for a plasmid, pChi603LMS1.
FIG. 18 shows the electrophoretic patterns in SDS-PAGE (using 4-15% gradient gels) of purified chimeric human anti-GM.sub.2 antibodies, KM966 and KM967. The patterns obtained under reducing conditions are shown on the left side and those obtained under nonreducing conditions on the right side. From the left, the lanes include low molecular weight markers, KM967 and KM966 (reducing conditions), and KM967 and KM966 (nonreducing conditions).
FIG. 19 shows the electrophoretic patterns in SDS-PAGE (using 4-15% gradient gels) of a purified chimeric human anti-GM.sub.2 antibody, KM968. The pattern obtained under reducing conditions is shown on the left side and that obtained under nonreducing conditions on the right side. From the left, the lanes include high molecular weight markers, low molecular weight markers, a standard human IgG, KM968 (reducing conditions), the same low molecular weight markers, the standard human IgG, and KM968 (nonreducing conditions).
FIG. 20 graphically shows the CDC (complement dependent cytotoxicity) activities of KM966 against the human lung small cell carcinoma cell lines SBC-3 and LU-135. The ordinate indicates the cytotoxic activity and the abscissa the concentration of the antibody added. The solid bars indicate the CDC activities of KM-696 and the shaded bars the CDC activities of KM966.
FIG. 21 graphically shows the CDC activities of KM966 against the human lung squamous cell carcinoma cell line PC-10 and human lung adenocarcinoma cell line RERF-LC-MS. The ordinate indicates the cytotoxicity and the abscissa the concentration of the antibody added. The solid bars indicate the CDC activities of KM-696 and the shaded bars the CDC activities of KM966.
FIG. 22 graphically shows the CDC activities of KM966 against the human lung large cell carcinoma cell line PC-13 and human neuroblastoma cell line NAGAI. The ordinate indicates the cytotoxic activity and the abscissa the concentration of the antibody added. The solid bars indicate the CDC activities of KM-696 and the shaded bars the CDC activities of KM966.
FIG. 23 graphically shows the CDC activities of KM966 against the human neuroblastoma cell line GOTO and human brain tumor cell line A172. The ordinate indicates the cytotoxic activity and the abscissa the concentration of the antibody added. The solid bars indicate the CDC activities of KM696 and the shaded bars the CDC activities of KM966.
FIG. 24 graphically shows the ADCC (antibody dependent cell mediated cytotoxicity) activities of KM966 against the human lung small cell carcinoma cell lines SBC-3 and LU-135. The ordinate indicates the cytotoxic activity and the abscissa the concentration of the antibody added. The solid bars indicate the ADCC activities of KM-696 and the shaded bars the ADCC activities of KM966.
FIG. 25 graphically shows the ADCC activities of KM966 against the human lung squamous carcinoma cell line PC-10 and human lung adenocarcinoma cell line RERF-LC-MS. The ordinate indicates the cytotoxic activity and the abscissa the concentration of the antibody added. The solid bars indicate the ADCC activities of KM-696 and the shaded bars the ADCC activities of KM966.
FIG. 26 graphically shows the ADCC activities of KM966 against the human lung large cell carcinoma cell line PC-13 and human neuroblastoma cell line NAGAI. The ordinate indicates the cytotoxicity and the abscissa the concentration of the antibody added. The solid bars indicate the ADCC activities of KM-696 and the shaded bars the ADCC activities of KM966.
FIG. 27 graphically shows the ADCC activities of KM966 against the human neuroblastoma cell line GOTO and human brain tumor cell line A172. The ordinate indicates the cytotoxicity and the abscissa the concentration of the antibody added. The solid bars indicate the ADCC activities of KM-696 and the shaded bars the ADCC activities of KM966.
FIG. 28 shows a restriction enzyme cleavage map of a 9.3 kb XbaI fragment of the KM50 cell chromosomal DNA.
FIG. 29 shows a construction scheme for a plasmid, pKMB11.
FIG. 30 shows a construction scheme for a plasmid, pKMD6.
FIG. 31 shows a construction scheme for a plasmid, pEPKMA1.
FIG. 32 shows a construction scheme for a plasmid, pEPKMB1.
FIG. 33 shows a construction scheme for a plasmid, pAGE501.
FIG. 34 shows a construction scheme for a plasmid, pAGE109.
FIG. 35 shows a construction scheme for a plasmid, pAGE502.
FIG. 36 shows a construction scheme for a plasmid, pAGE503.
FIG. 37 shows a construction scheme for a plasmid, pSEd1.
FIG. 38 shows a construction scheme for a plasmid, pSE1D2.
FIG. 39 shows a construction scheme for a plasmid, pIG1SE1d2.
FIG. 40 shows a construction scheme for a plasmid, pIG1SE1d3.
FIG. 41 shows a construction scheme for a plasmid, pIG1SE1d4.
FIG. 42 shows a construction scheme for a plasmid, pPMOL2.
FIG. 43 shows a construction scheme for a plasmid, pPMOL3.
FIG. 44 shows a construction scheme for a plasmid, pchCKA7.
FIG. 45 shows a construction scheme for a plasmid, pchCKB1 (SEQ ID NO:102 and SEQ ID NO:103).
FIG. 46 shows a construction scheme for a plasmid, pckCKC1.
FIG. 47 shows a construction scheme for a plasmid, pChiIgHB2.
FIG. 48 shows a construction scheme for a plasmid, pChiIgLA1.
FIG. 49 shows a construction scheme for plasmids, pKM641HA3 and pKM641LA2.
FIG. 50 shows a construction scheme for a plasmid, pChi641HA1.
FIG. 51 shows a construction scheme for a plasmid, pKM641HE1.
FIG. 52 shows a construction scheme for a plasmid, pKM641HF1.
FIG. 53 shows a construction scheme for a plasmid, pChi641HA1.
FIG. 54 shows a construction scheme for a plasmid, pChi641HAM1.
FIG. 55 shows a construction scheme for a DNA, hKM796H.
FIG. 56 shows a construction scheme for a DNA, hKM796L.
FIG. 57 shows a construction scheme for a plasmid, phKM796HM1.
FIG. 58 shows a construction scheme for a plasmid, phKM796HMS1.
FIG. 59 shows a construction scheme for a plasmid, phKM796LI1.
FIG. 60 shows a construction scheme for a plasmid, phKM796LM1.
FIG. 61 shows a construction scheme for a plasmid, phKM796LMS1.
FIG. 62 shows a constfuction scheme for a plasmid, phKM796H107.
FIG. 63 shows a construction scheme for a plasmid, phKM796HL1.
FIG. 64 shows a construction scheme for a plasmid named pBSA.
FIG. 65 shows a construction scheme for a plasmid named pBSAE.
FIG. 66 shows a construction scheme for a plasmid named pBSH-S.
FIG. 67 shows a construction scheme for a plasmid named pBSK-H.
FIG. 68 shows a construction scheme for plasmids named pBSH-SA and pBSK-HA.
FIG. 69 shows a construction scheme for plasmids named pBSH-SAE and pBSK-HAE.
FIG. 70 shows a construction scheme for plasmids named pBSH-SAEE and pBSK-HAEE.
FIG. 71 shows a construction scheme for a plasmid named pBSK-HAEESal.
FIG. 72 shows a construction scheme for a plasmid named pBSX-S.
FIG. 73 shows a construction scheme for a plasmid named pBSX-SA.
FIG. 74 shows a construction scheme for a plasmid named pBSSC.
FIG. 75 shows a construction scheme for a plasmid named pBSMo.
FIG. 76 shows a construction scheme for a plasmid named pBSMoS.
FIG. 77 shows a construction scheme for a plasmid named pChiIgLA1S.
FIG. 78 shows a construction scheme for a plasmid named pMohC.kappa..
FIG. 79 shows a construction scheme for a plasmid named pBSMoSal.
FIG. 80 shows a construction scheme for a plasmid named pBSMoSalS.
FIG. 81 shows a construction scheme for a plasmid named pBShC.gamma.1.
FIG. 82 shows a construction scheme for a plasmid named pMohC.gamma.1.
FIG. 83 shows a construction scheme for a plasmid named pMo.gamma.1SP.
FIG. 84 shows a construction scheme for a plasmid named pMo.kappa..gamma.1SP.
FIG. 85 shows a construction scheme for a plasmid named pKANTEX93.
FIG. 86 shows a construction scheme for a plasmid named pBSNA.
FIG. 87 shows a construction scheme for a plasmid named pBSH3.
FIG. 88 shows a construction scheme for a plasmid named pBSES.
FIG. 89 shows a construction scheme for a plasmid named pESL3.
FIG. 90 shows a construction scheme for a plasmid named pKANTEX796H.
FIG. 91 shows a construction scheme for a plasmid named pKANTEX796.
FIG. 92 shows a construction scheme for a plasmid named pT796.
FIG. 93 is a graphic representation of transient human anti-GM.sub.2 chimera antibody expression by the plasmids pKANTEX796 and pT796. The ordinate donotes the antibody concentration that showed GM.sub.2 -binding activity, and the abscissa denotes the time after introduction of the plasmid.
FIG. 94 shows a construction scheme for a plasmid named pBSH10.
FIG. 95 shows a construction scheme for a plasmid named pBSL16.
FIG. 96 illustrates a process for mutagenesis by PCR and a process for cloning DNA fragments mutated.
FIG. 97 shows a construction scheme for a plasmid named pBSLV1+2.
FIG. 98 shows a construction scheme for a plasmid named pBSLm-28.
FIG. 99 shows a construction scheme for a plasmid named pBSHSGL.
FIG. 100 shows a construction scheme for a plasmid named pT796LCDR.
FIG. 101 shows a construction scheme for plasmids named pT796HLCDR, pT796HLCDRHV2 and pT796HLCDRHV4.
FIG. 102 shows a construction scheme for a plasmid named pT796HLCDRH10.
FIG. 103 shows construction scheme for plasmids named pT796HCDR, pT796HCDRHV2, pT796HCDRHV4 and pT796HCDRH10.
FIG. 104 is a graphic representation of the results of human CDR-transplanted anti-GM.sub.2 antibody activity evaluation in terms of transient expression as obtained using the plasmids pT796, pT796HCDR, pT796HCDRHV2, pT796HCDRHV4 and pT796HCDRH10. The ordinate denotes the plasmid used, and the abscissa denotes the relative activity value with the activity obtained with the chimera antibody being taken as 100%.
FIG. 105 shows a construction scheme for plasmids named pT796HLCDRLV1, pT796HLCDRLV2, pT796HLCDRLV3, pT796HLCDRLV4, pT796HLCDRLV8, pT796HLCDRLm-2, pT796HLCDRLm-8, pT796HLCDRLm-28 and pT796HLCDRHSGL.
FIG. 106 is a graphic representation of the results of human CDR-transplanted anti-GM.sub.2 antibody activity evaluation in terms of transient expression as obtained using the plasmids pT796, pT796HLCDR, pT796HLCDRLV1, pT796HLCDRLV2, pT796HLCDRLV3, pT796HLCDRLV4, pT796HLCDRLV8, pT796HLCDRLm-2, pT796HLCDRLm-8, pT796HLCDRLm-28 and pT796HLCDRHSGL. The ordinate denotes the plasmid used, and the abscissa denotes the relative activity value with the activity obtained with the chimera antibody being taken as 100%.
FIG. 107 shows a construction scheme for plasmids named pKANTEX796HLCDRLm-28 and pKANTEX796HLCDRHSGL.
FIG. 108 shows electrophoretic patterns obtained for human anti-GM.sub.2 chimera antibody KM966 and purified human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967 by SDS-PAGE (4 to 15% gradient gels used). The patterns shown on the left side are those obtained under reducing conditions, and those on the right under nonreducing conditions. From the left of each lane, the electrophoretic patterns for high-molecular-weight marker, KM966, KM8966, KM8967, low-molecular-weight marker, KM966, KM8966 and KM8967 are shown in that order.
FIG. 109 is a graphic representation of the GM.sub.2 -binding activities of human anti-GM.sub.2 chimera antibody KM966 and purified human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967. The ordinate denotes the GM.sub.2 -binding activity, and the abscissa the antibody concentration. The plots .smallcircle., .circle-solid. and .DELTA. stand for the GM.sub.2 -binding activities of KM966, KM8966 and KM8967, respectively.
FIG. 110 is a graphic representation of the reactivities of human anti-GM.sub.2 chimera antibody KM966 and purified human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967 against various gangliosides. The ordinate denotes the ganglioside species, and the abscissa the binding activity. AcGM2 stands for N-acetyl-GM.sub.2, GcGM2 for N-glycolyl-GM.sub.2, AcGM3 for N-acetyl-GM.sub.3 and GcGM3 for N-glycolyl-GM.sub.3. The plots .quadrature., .box-solid. and .quadrature. stand for the reactivities of KM966, KM8966 and KM8967, respectively.
FIG. 111 is a graphic representation of the reactivities of human anti-GM.sub.2 chimera antibody KM966 and purified human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967 against the human lung small cell carcinoma cell line SBC-3. The ordinate denotes the number of cells, and the abscissa the fluorescence intensity. From the lowermost graph, the reactivities of control, KM8967, KM8966 and KM966 are shown in that order.

DETAILED DESCRIPTION OF THE INVENTION
The present invention relates to humanized antibodies specific for the ganglioside GM.sub.2. The antibodies can be of any of the immunoglobulin (Ig) classes, it is preferable, however, that the antibodies be of the IgG type. The term "humanized antibody", as used herein, includes within its meaning, chimeric human antibody and CDR-grafted antibody. Chimeric human antibodies of the invention include the V.sub.H and V.sub.L of an antibody of an animal other than a human and the C.sub.H and C.sub.L of a human antibody. The CDR-transplanted antibodies of the invention result from the replacement of CDRs of the V.sub.H and V.sub.L of a human antibody with those of the V.sub.H and V.sub.L, respectively, of an antibody of an animal other than a human.
An example of a chimeric human antibody of the invention is an antibody the V.sub.H of which contains an amino acid sequence segment as defined by SEQ ID NO:91, including the 1st to 120th amino acids of that sequence, and the V.sub.L of which contains an amino acid sequence segment as defined by SEQ ID NO:92, including the 1st to 107th amino acids of that sequence.
An example of a CDR-transplanted antibody of the invention is an antibody the V.sub.H CDRs of which have the amino acid sequences defined by SEQ ID NO:94, SEQ ID NO:95 and SEQ ID NO:96 and the V.sub.L CDRs of which have the amino acid sequences defined by SEQ ID NO:97, SEQ ID NO:98 and SEQ ID NO:99.
The chimeric human antibodies of the invention can be produced in the following manner:
(1) Preparation of cDNAs coding for the V.sub.H and V.sub.L of an antibody of nonhuman animal
cDNAs coding for the V.sub.H and V.sub.L of an antibody of a nonhuman animal, for example a mouse anti-GM.sub.2 monoclonal antibody, can be prepared as follows.
mRNAs can be extracted from hybridomas producing the mouse anti-GM.sub.2 monoclonal antibody, for example hybridomas producing the mouse anti-GM.sub.2 monoclonal antibody KM796, and cDNAs reverse transcribed therefrom. Using the cDNAs, a library can be constructed using phage or plasmid vectors. The recombinant phage or recombinant plasmid containing the cDNA coding for the V.sub.H, and the recombinant phage or recombinant plasmid containing the cDNA coding for the V.sub.L can be isolated from the library using a constant region portion or a variable region portion of an antibody of a nonhuman animal, for example a mouse antibody, as a probe. The base sequences of the V.sub.H -encoding cDNA and V.sub.L -encoding cDNA in the recombinant phage or recombinant plasmid can then be determined. Examples of the nonhuman animals include mice, rats, hamsters and monkeys.
(2) Construction of a vector for chimeric human antibody expression
Expression of chimeric human antibody H chain and L chains can be effected using expression vectors suitable for use in animal cells, inserted into which are the cDNAs coding for the human C.sub.H and C.sub.L. Any expression vector suitable for use in animal cells can be used, provided that it allows integration and expression of the human antibody constant region-encoding cDNAs. Examples include pAGE107 �Cytotechnology, 3, 133 (1990)!, pAGE103 �J. Biochem., 101, 1307 (1987)!, pHSG274 �Gene, 27, 223 (1984)!, pKCR �Proc. Natl. Acad. Sci. U.S.A., 78, 1527 (1981)! and pSG1.beta.d2-4 �Cytotechnology, 4, 173 (1990)!, among others. Examples of promoters and enhancers suitable for use in such expression vectors include the SV40 early promoter and enhancer �J. Biochem., 101, 1307 (1987)!, the Moloney mouse leukemia virus LTR (long terminal repeat) promoter and enhancer �Biochem. Biophys. Res. Commun., 149, 960 (1987)! and the immunoglobulin H chain promoter �Cell, 41, 479 (1985)! and enhancer �Cell, 33, 717 (1983)!. The promoters and enhancers are located in the expression vector in operable linkage with the coding sequences.
(3) Construction of a chimeric human antibody expression vector
The vector for chimeric human antibody H chain and L chain expression, as obtained in (2), is provided with a cloning site upstream of the human constant region, for insertion of a cDNA coding for the variable region of an antibody of a nonhuman animal. Insertion, at this cloning site, of the cDNA coding for the variable region of a nonhuman animal antibody, using a synthetic DNA comprising a 5' terminal base sequence of the human antibody constant region and a 3' terminal base sequence of the variable region of the nonhuman animal antibody and having restriction enzyme sites on both ends, gives a chimeric human antibody expression vector with the cDNA coding for the human antibody constant region and the cDNA coding for the variable region of the nonhuman animal antibody joinedly inserted therein via the synthetic DNA for producing appropriate restriction enzyme sites. The synthetic DNA can be synthesized using a DNA synthesizer based on the 5' terminal base sequence of the human antibody constant region and the base sequence of said 3' terminal base sequence of the nonhuman animal antibody variable region.
(4) Construction of a chimeric human antibody H chain expression vector
A vector for chimeric human antibody H chain expression is constructed, for example, by excising that portion of the human antibody C.sub.H -encoding cDNA which covers from the ApaI site near the 5' terminus to the 3' terminus and inserting that portion into an expression vector suitable for use in animal cells. This vector for chimeric human antibody H chain expression is provided with a cloning site for insertion of a cDNA coding for a nonhuman animal V.sub.H. cDNA coding for the nonhuman animal V.sub.H, excised using an appropriate restriction enzyme, is inserted into the vector at the cloning site using a synthetic DNA comprising that portion of the human antibody C.sub.H gene which covers from the 5' terminus to the ApaI site and the base sequence of a 3' terminal portion of the nonhuman animal antibody V.sub.H gene and having restriction enzyme sites on both ends, to give a chimeric human antibody H chain expression vector which allows no change in the amino acid sequence of V.sub.H upon expression thereof and has appropriate restriction enzyme sites.
(5) Construction of a chimeric human antibody L chain expression vector
A vector for chimeric human antibody L chain expression is constructed, for example by introducing an EcoRV site into the human antibody C.sub.L -encoding cDNA in the vicinity of the 5' terminus by mutagenesis, excising that portion which covers from the EcoRV site to the 3' terminus and inserting that portion into a plasmid, such as the plasmid pIg1SE1d4. This vector for chimeric human antibody L chain expression is provided with a cloning site for insertion of the cDNA coding for nonhuman animal V.sub.L. The nonhuman animal antibody V.sub.L -encoding cDNA, excised with an appropriate restriction enzyme, is inserted into the vector at the cloning site using a synthetic DNA comprising that portion of the human antibody C.sub.L gene which covers from the 5' terminus to the EcoRV site and the base sequence of a 3' terminal portion of the nonhuman animal antibody V.sub.L gene and having restriction enzyme sites on both ends, to give a chimeric human antibody L chain expression vector which allows no change in the amino acid sequence of V.sub.L upon expression thereof.
(6) Introduction of the chimeric human antibody expression vectors into host cells
Introduction of the chimeric human antibody H chain expression vector and chimeric human antibody L chain expression vector into host cells gives a transformant producing the chimeric human antibody. In introducing the vectors into host cells, a splicing signal may be introduced into the chimeric human antibody H chain and L chain expression vectors for mRNA stabilization �Cell, 17, 737 (1979)!.
The chimeric human antibody H chain and L chain vectors can be introduced into host cells, for example, simultaneously by electroporation �JP-A-2-257891 (the term "JP-A" used herein means an unexamined published Japanese patent application.); Cytotechnology, 3, 133 (1990)!. In addition, an expression vector containing genes coding for both the chimeric human antibody H chain and L chain �tandem expression vector! can be introduced into host cells �BIO/TECHNOLOGY, 9, 64 (1991)!. The use of a tandem expression vector is preferred since a higher level of chimeric human antibody expression can be attained thereby, with approximately equal H chain and L chain expression levels.
An example of a method of producing the CDR-transplanted antibodies of the invention is described as follows.
First, a CDR-transplanted antibody expression vector can be constructed by the method of Winter et al. �Nature, 332, 323 (1988)! as follows.
Three synthetic DNAs are constructed designed so as to comprise the cDNAs coding for three CDR peptides of the V.sub.H of a nonhuman animal antibody, for example, peptides having the amino acid sequences defined by SEQ ID NO:94, SEQ ID NO:95 and SEQ ID NO:96, with DNAs coding for amino acid sequences comprising of several amino acids from both ends of the corresponding CDRs of the V.sub.H of a human antibody being located at the respective both ends of the cDNAs, DNA synthesis is carried out with a plasmid containing the human antibody V.sub.H gene as a template. An example of the human antibody V.sub.H gene-containing plasmid is the M13 plasmid containing a human antibody NEW gene-derived sequence �J. Biol. Chem., 253, 585 (1978); Nature, 332, 323 (1988)!.
The DNA obtained is inserted into the vector for chimeric human antibody H chain expression in the same manner as in the construction of the chimeric human antibody expression vector mentioned above to give a CDR-transplanted antibody H chain expression vector.
Similarly, using, as primers, three synthetic DNAs designed to comprise the cDNAs coding for three CDR peptides of the V.sub.L of a nonhuman animal antibody, for example, the peptides having the amino acid sequences defined by SEQ ID NO:97, SEQ ID NO:98 and SEQ ID NO:99, with DNAs coding for amino acid sequences comprising several amino acids from both ends of the corresponding CDRs of the human antibody V.sub.L being located at the respective both ends of said cDNAs, DNA synthesis is carried out with a human antibody V.sub.L gene-containing plasmid as a template. An example of the human antibody V.sub.L gene-containing plasmid is the M13 plasmid containing a human myeloma protein (Bence-Jones protein) REI gene-derived sequence �Eur. J. Biochem., 45, 513 (1974); Nature, 332, 323 (1988)!.
By inserting the DNA obtained into a vector for chimeric human L chain expression in the same manner as described in respect of the construction of the chimeric human antibody expression vector, a CDR-transplanted antibody L chain expression vector can be constructed.
It is also possible to construct the CDR-transplanted antibody H chain and L chain expression vectors by synthesizing DNAs coding for the peptides having amino acid sequences resulting from replacement of the three CDRs each of the H chain and L chain of a human antibody with the corresponding CDRs of the H chain and L chain of a nonhuman animal antibody and then inserting the DNAs into a vector for chimeric human antibody H chain or L chain expression in the same manner as described in respect of the construction of the chimeric human antibody expression vector mentioned above.
The CDR-transplanted antibody expression vector can be introduced into host cells in the same manner as the chimeric human antibody expression vector to give a transformant producing the CDR-transplanted antibody.
The host cells suited for the introduction thereinto of the chimeric human antibody or CDR-transplanted antibody expression vector may be any host cells provided that the chimeric human antibody or CDR-transplanted antibody can be expressed therein. Examples include mouse SP2/0-Ag14 cells (ATCC CRL1581; hereinafter, "SP2/0 cells"), mouse P3X63-Ag8.653 cells (ATCC CRL1580), CHO cells deficient in the dihydrofolate reductase gene (hereinafter, "dhfr") �Urlaub et al.: Proc. Natl. Acad. Sci. U.S.A., 77, 4216 (1980)! and rat YB2/3HL.P2.G11.16Ag.20 cells (ATCC CRL1662; hereinafter, "YB2/0 cells"), with YB2/0 cells being preferred.
The transformants producing the chimeric human antibody or CDR-transplanted antibody are selected by the method disclosed in JP-A-2-257891 using PRMI1640 medium containing G418 and fetal calf serum. A particular example of the chimeric human antibody-producing transformant is the transformant KM966 producing a chimeric human antibody that reacts with the ganglioside GM.sub.2. Examples of human CDR-transplanted antibody-producing transformants include the transformants KM8966 and KM8967 each producing a human CDR-transplanted antibody that reacts with the ganglioside GM.sub.2. KM966 has been deposited with the Fermentation Research Institute, Agency of Industrial Science and Technology, of 1-3, Higashi 1-chome, Tsukuba-shi, Ibaraki 305 JAPAN, as of Jul. 15, 1992 under the deposit number FERM BP-3931. KM8966 and KM8967 have also deposited with the above-described institute as of May 23, 1995 under the deposit numbers FERM BP-5105 and FERM BP-5106, respectively.
When the transformant obtained is cultivated in a medium, the chimeric human antibody or CDR-transplanted antibody can be produced and accumulated in the culture fluid. The activity of the chimeric human antibody or CDR-transplanted antibody in the medium can be determined by an enzyme-linked immunosorbent assay (ELISA; E. Harlow et al. (ed.): Antibodies--A Laboratory Manual, Cold Spring Harbor Laboratory, 1988). The antibody productivity of the transformant can be increased by utilizing a dhfr amplification system as disclosed in JP-A-2-257891.
The chimeric human antibody and CDR-transplanted antibody can be purified from the culture supernatants obtained as mentioned above using a protein A column (E. Harlow et al. (ed.): Antibodies--A Laboratory Manual, Cold Spring Harbor Laboratory, 1988). As noted above, the chimeric human antibody KM966, which reacts with the ganglioside GM.sub.2, is a specific example of the thus-obtained chimeric human antibodies and CDR-transplanted antibodies.
The reactivity of the chimeric human antibody or CDR-transplanted antibody of the invention can be checked by ELISA. The molecuar weight of the purified antibody H chain or L chain or whole antibody molecule can be determined by polyacrylamide gel electrophoresis (SDS-PAGE) or Western blotting (E. Harlow et al. (ed.): Antibodies--A Laboratory Manual, Cold Spring Harbor Laboratory, 1988).
The binding activity of the chimeric human antibody or CDR-transplanted antibody that reacts with the ganglioside GM.sub.2 of cultured cancer cells can be measured, for example, by the fluorescent antibody technique or by ELISA. The complement dependent cytotoxic activity (CDC activity) and antibody dependent cell mediated cytotoxic activity (ADCC activity) of the chimeric human antibody or CDR-transplanted antibody are measured by the methods of Ohta et al. �Cancer Immunol. Immunother., 36, 260 (1993)!.
The humanized antibodies of the invention specifically bind to human cancer cells and exhibit CDC activity and ADCC activity against human cancer cells and therefore are useful in the treatment of human cancers, among others.
The humanized antibodies according to the present invention can be used alone as an anticancer agent. They may be formulated into an anticancer composition together with at least one pharmaceutically acceptable carrier. For instance, the humanized antibodies are dissolved in physiological saline, an aqueous solution of glucose, lactose or mannitol and the like. The powder of the humanized antibodies for injection can be prepared by lyophilizing the humanized antibodies in accordance with the conventional method and mixing the lyophilized products with sodium chloride. The anticancer composition may further contain additives conventionally used well known in the art of medical preparation, for example, pharmaceutically acceptable salts.
The humanized antibodies according to the present invention can be administered in the form of the above-described anticancer composition to mammals including human in a dose of 0.2 to 20 mg/kg/day. The dose may vary depending on the age, condition, etc. of patients. The administration of the anticancer composition can be effected by intravenous injection once a day (single administration or consecutive administration) or intermittently one to three times a week or once every two to three weeks.
The anticancer composition is expected to be useful for treating cancer such as melanoma, neuroblastoma and glioma.
The following Examples and Reference Examples are further illustrative of the present invention, but are not to be construed to limit the scope of the present invention.
EXAMPLE 1
Production of Chimeric Human Anti-GM.sub.2 Antibodies
1. Isolation of mRNAs From Hybridoma Cells Producing the Mouse Anti-GM.sub.2 Monoclonal Antibody KM-796 or KM-750 and From Hybridoma Cells Producing the Rat Anti-GM.sub.2 Monoclonal Antibody KM-603
Using mRNA extraction kit Fast Track (product number K1593-02) manufactured by Invitorogen and following the description of the manual attached to the kit, mRNAs were isolated from 1.times.10.sup.8 cells each of the mouse anti-GM.sub.2 monoclonal antibody KM-796-producing hybridoma cell line (FERM BP-3340), the mouse anti-GM.sub.2 monoclonal antibody KM-750-producing hybridoma cell line (FERM BP-3339) and the rat anti-GM.sub.2 monoclonal antibody KM-603-producing hybridoma cell line (FERM BP-2636).
2. Construction of Monoclonal Antibody KM-796 and KM-750 H Chain and L Chain cDNA Libraries
Using cDNA Synthesis Kit (product number 27-9260-01) manufactured by Pharmacia and following the manual attached to the kit, cDNA having the EcoRI adapter on both ends was synthesized from 5 .mu.g each of the KM-796- and KM-750-derived mRNAs obtained as described in Paragraph 1 above. About 6 .mu.g of each cDNA product obtained was dissolved in 10 .mu.l of sterilized water and fractionated by agarose gel electrophoresis, and a cDNA fragment (about 1.8 kb) corresponding to the IgG antibody H chain and a cDNA fragment (about 1.0 kb) corresponding to the L chain were recovered (about 0.1 .mu.g each). Then, 0.1 .mu.g of each cDNA fragment of about 1.8 kb and 0.1 .mu.g of each cDNA fragment of about 1.0 kb were respectively dissolved in 11.5 .mu.l of T4 ligase buffer, together with 1 .mu.g of the Lambda ZAPII vector (cleaved with EcoRI and then treated with calf intestine alkaline phosphatase; product of Stratagene). After addition of 175 units of T4 DNA ligase, each solution was incubated at 12.degree. C. for 24 hours and then at room temperature for 2 hours. A 4-.mu.l portion of each reaction mixture was subjected to packaging into the lambda phage in the conventional manner �Maniatis et al. (ed.): Molecular Cloning, 2.95 Cold pring Harbor Laboratory, 1989! using Giga Pak Gold (Stratagene), followed by transfection, in the conventional manner �Maniatis et al. (ed.): Molecular Cloning, 2.95-107, Cold Spring Harbor Laboratory, 1989! of the Escherichia coli strain XL1-Blue �Biotechniques, 5, 376 (1987)! attached to Giga Pak Gold, to give about 4.times.10.sup.3 phage clones each as a KM-796 or KM-750 H chain or L chain cDNA library. Then the phage clones of each library were fixed on a nitrocellulose filter in the conventional manner �Maniatis et al. (ed.): Molecular Cloning, 2.112, Cold Spring Harbor Laboratory, 1989!.
3. Construction of KM-603 H Chain and L Chain cDNA Libraries
Using 5 ug of the KM-603 MRNA obtained as mentioned above in Paragraph 1 and cDNA Synthesis Kit (product number 27-9260-01) manufactured by Pharmacia, cDNA having the EcoRI adapter on both ends was synthesized. About 6 .mu.g of the cDNA produced was dissolved in 10 .mu.l of sterilized water and fractionated by agarose gel electrophoresis. A cDNA fragment (about 2.2 kb) corresponding to the IgG antibody H chain and a cDNA fragment (about 1.0 kb) corresponding to the L chain were recovered (about 0.1 .mu.g each). Then 0.1 .mu.g of the cDNA fragment of about 2.2 kb and 0.1 .mu.g of the cDNA fragment of about 1.0 kb were respectively dissolved in 11.5 .mu.l of T4 ligase buffer, together with 1 .mu.g of the Lambda ZAPII vector (cleaved with EcoRI and then treated with calf intestine alkaline phosphatase; product of Stratagene) and, after addition of 175 units of T4 DNA ligase, the resultant solution was incubated at 12.degree. C. for 24 hours and then at room temperature for 2 hours. A 4-.mu.l portion of each reaction mixture was subjected to packaging into the lambda phage in the conventional manner �Maniatis et al. (ed.): Molecular Cloning, 2.95, Cold Spring Harbor Laboratory, 1989! using Giag Pak Gold (Stratagene), followed by transfection, in the conventional manner �Maniatis et al. (ed.): Molecular Cloning, 2.95-107, Cold Spring Harbor Laboratory, 1989!, of the Escherichia coli strain XL-Blue attached to Giga Pak Gold, whereby about 1.times.10.sup.4 phage clones were obtained each as a KM-603 H chain or L chain cDNA library. Then, the phage clones of each library were fixed on a nitrocellulose filter in the conventional manner �Maniatis et al. (ed.): Molecular Cloning, 2.112, Cold Spring Harbor Laboratory, 1989!.
4. Cloning of the KM-796 and KM-750 H Chain and L Chain cDNAs
From among the KM-796 and KM-750 H chain cDNA libraries and L chain cDNA libraries constructed as described above in Paragraph 2, phage clones firmly bound at 65.degree. C. to a probe prepared by labeling a mouse immunoglobulin constant region cDNA �for the H chain, the BamHI-XhoI fragment of the mouse C.gamma.3 cDNA (Wels et al: EMBO J., 3, 2041-2046, 1984); for the L chain, the HpaI-XhoI fragment of the mouse C.kappa. cDNA (Hieter et at.: Cell, 22, 197-207, 1980)! with .sup.32 P were recovered in the conventional manner �Maniatis et al.: Molecular Cloning, 2.108, Cold Spring Harbor Laboratory, 1989!. Then, using a ZAP-cDNA Synthesis Kit (cDNA synthesis kit; product number sc200400) manufactured by Stratagene, phage clones were converted into pBluescript plasmids, and a KM-796 H chain cDNA-containing recombinant plasmid (pKM796H1) and a KM-796 L chain cDNA-containing recombinant plasmid (pKM796L1) (FIG. 1) as well as a KM-750 H chain cDNA-containing recombinant plasmid (pKM750H1) and a KM-750 L chain cDNA-containing recombinant plasmid (pKM750L1) (FIG. 2) were obtained. Cleavage of pKM796H1, pKM750H1, pKM796L1 and pKM750L1 with EcoRI revealed that a cDNA fragment of about 1.8 kb had been inserted into pKM796H1 and pKM750H1 and a cDNA fragment of about 0.9 kb into pKM796L1 and pKM750L1.
5. Cloning of KM-603 H Chain and L Chain cDNAs
Phage clones firmly bound at 65.degree. C. to a probe prepared by labeling a mouse immunoglobulin constant region chromosomal gene �mouse C.mu. gene-containing SmaI-KpnI fragment of about 11.5 kb (Kataoka et al.: Proc. Natl. Acad. Sci. U.S.A., 77, 919-923, 1980) and mouse C.kappa. gene-containing HindIII-BamHI fragment of about 3 kb (Sakano et al.: Nature, 280, 288, 1979)! with .sup.32 P were isolated from the KM-603 H chain cDNA library and L chain cDNA library constructed as mentioned above in Paragraph 3 in the conventional manner �Maniatis et al. (ed.): Molecular Cloning, 2.108, Cold Spring Harbor Laboratory, 1989!. Then, using ZAP-cDNA Synthesis kit (product number sc200400) manufactured by Stratagene, the phage clones were converted to pBluescript plasmids and a KM-603 H chain cDNA-containing recombinant plasmid, pKM603H1, and a KM-603 L chain cDNA-containing recombinant plasmid, pKM603L1, were obtained (FIG. 3). Cleavage of pKM603H1 and pKM603L1 revealed that pKM603H1 contained a cDNA fragment of about 2.0 kb as inserted therein and pKM603L1 a cDNA fragment of about 0.9 kb as inserted therein.
6. Base Sequences of the Variable Regions in the H Chain cDNA and L Chain cDNA
The base sequences of the variable regions in the H chain cDNA and L chain cDNA obtained as mentioned above in Paragraphs 4 and 5 were determined by the dideoxy method �Maniatis et al. (ed.): Molecular Cloning, 13.42, Cold Spring Harbor Laboratory, 1989! using Sequenase Version 2.0 DNA Sequencing Kit manufactured by United States Biochemical Corporation. All the cDNA had a methionine codon, presumably the initiation codon ATG, at the 5' terminus and were leader sequence-containing full-length cDNAs. Based on the base sequences of the respective cDNAs, the amino acid sequences of the H chain and L chain of KM-796, KM-750 and KM-603 were deduced. The amino acid sequence of the KM-796 H chain is shown in SEQ ID NO:91, that of the L chain of KM-796 and KM-750 in SEQ ID NO:92, that of the KM-750 H chain in SEQ ID NO:93, that of the KM-603 H chain in SEQ ID NO:4 and that of the KM-603 L chain in SEQ ID NO:5.
7. Construction of KM-796- and KM-750-Derived Chimeric Human Antibody H Chain and L Chain Expression Vectors
(1) Construction of a vector, pAGE147, carrying the Moloney mouse leukemia virus terminal repeat promoter/enhancer
The plasmid pPMOL1 (2 .mu.g), described in JP-A-1-63394, was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 6 mM 2-mercaptoethanol, 20 units of SmaI was added, and digestion was carried out at 30.degree. C. for 3 hours. Then, sodium chloride was added to a concentration of 50 mM, 20 units of ClaI was added, and digestion was conducted at 37.degree. C. for 2 hours. The reaction mixture was subjected to agarose gel electrophoresis, and a DNA fragment (about 0.6 kb) containing the Moloney mouse leukemia virus terminal repeat promoter/enhancer was recovered.
Then, the following two synthetic DNAs were synthesized using an automatic DNA synthesizer (model 380A manufactured by Applied Biosystems Co., Ltd.). ##STR1##
The thus-obtained synthetic DNAs (25 picomoles each) were dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.6) containing 10 mM magnesium chloride, 5 mM DTT (dithiothreitol), 0.1 mM EDTA and 0.5 mM adenosine triphosphate (hereinafter, "ATP"), 5 units of T4 DNA kinase was added, and 5'-phosphorylation was carried out at 37.degree. C. for 30 minutes.
The plasmid pPMOL1-derived ClaI-SmaI fragment (0.6 kb, 0.05 .mu.g) and two 5'-phosphorylated synthetic DNAs (1 picomole each), obtained as described above, and a HindIII linker (5'-pCAAGCTTG-3'; Takara Shuzo) (1 picomole) were dissolved in 30 .mu.l of 66 mM Tris-hydrochloride buffer (pH 7.5) containing 6.6 mM magnesium chloride, 10 mM DTT and 0.1 mM ATP, 200 units of T4 DNA ligase (Takara Shuzo; hereinafter the same shall apply) were added, and ligation was carried out at 12.degree. C. for 16 hours. The resultant DNA fragment was recovered by ethanol precipitation and dissolved in 20 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride, 100 mM sodium chloride and 6 mM 2-mercaptoethanol, 10 units of HindIII and 10 units of XhoI were added, and digestion was carried out at 37.degree. C. for 2 hours. The reaction was terminated by phenol-chloroform extraction, and the DNA fragment was recovered by ethanol precipitation.
Separately, 1 .mu.g of the plasmid pAGE107 �Cytotechnology, 3, 133 (1990)! was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride, 100 mM sodium chloride and 6 mM 2-mercaptoethanol, 10 units of HindIII and 10 units of XhoI were added, and digestion was carried out at 37.degree. C. for 2 hours. The reaction mixture was subjected to agarose gel electrophoresis, and a DNA fragment (about 6.0 kb) containing the G418 resistance gene and ampicillin (hereinafter, "Ap") resistance gene was recovered.
The plasmid pAGE107-derived HindIII-XhoI fragment (6.0 kb, 0.3 .mu.g) and plasmid pPMOL1-derived HindIII-XhoI fragment (0.63 kb, 0.01 .mu.g) obtained as mentioned above were dissolved in 20 .mu.l of 66 mM Tris-hydrochloride buffer (pH 7.5) containing 6.6 mM magnesium chloride, 10 mM DTT and 0.1 mM ATP, 200 units of T4 DNA ligase were added, and ligation was carried out at 12.degree. C. for 16 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101, and the plasmid pAGE147 shown in FIG. 4 was obtained.
(2) Construction of a vector, pAGE148, carrying the .beta.-globin 3' splicing signal (SP)
For introducing the .beta.-globin 3' splicing signal into the chimeric human antibody expression vector at a site downstream from the antibody constant region gene, a vector (pAGE148), was constructed as follows, which contained the .beta.-globin 3' splicing signal and the same genes as those in the chimeric human antibody expression vector (except for the human antibody constant region gene).
Two .mu.g of pSE1UK1SEd1-3, described in JP-A-2-257851, were added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT. After addition of 10 units of HindIII, digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation. The precipitate was dissolved in 20 .mu.l of DNA polymerase I buffer, 5 units of Escheichia coli-derived DNA polymerase I Klenow fragment were added, and the 5' cohesive ends produced by HindIII digestion were rendered blunt by incubation at 22.degree. C. for 30 minutes. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT and 10 units of KpnI were added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT and 10 units of XhoI were added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and two DNA fragments, about 6.67 kb and about 1.98 kb in size, were recovered (about 0.2 .mu.g each).
Then, 2 .mu.g of pAGE147 obtained in (1) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of KpnI was added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT and 10 units of XhoI were added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.2 .mu.g of a DNA fragment of about 0.66 kb was recovered.
Then, 0.1 .mu.g of the XhoI-HindIII fragment (about 6.67 kb) of pSE1UK1SEd1-3, as obtained above, 0.1 .mu.g of the KpnI-HindIII fragment (about 1.98 kb), obtained above, and 0.1 .mu.g of the XhoI-KpnI fragment (about 0.66 kb) of pAGE147, as obtained above, were dissolved in a total of 20 .mu.l of T4 ligase buffer. Three hundred fifty units of T4 ligase were added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101, and the plasmid pAGE148 shown in FIG. 5 was obtained.
(3) Construction of KM-796- and KM-750-derived chimeric human antibody H chain expression vectors
First, the cDNA coding for the antibody variable region in the plasmid pKM796H1 or pKM750H1 was excised by cleavage at the 5'-terminal EcoRI site and the MaeIII site near the 3' end of said cDNA and joined, together with a synthetic DNA having the base sequence shown in SEQ ID NO:12, to the chimeric human antibody H chain expression vector pChi641HAM1, as follows (FIG. 6).
Three .mu.g of pKM796H1 or pKM750H1, obtained in Paragraph 4, were added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT. Further, 10 units of EcoRI and 10 units of MaeIII were added, and digestion was effected at 37.degree.0 C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 0.43 kb was recovered. Then, 3 .mu.g of pChi641HAM1, obtained in Reference Example 2, was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of ApaI were also added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1.0 .mu.g of a DNA fragment of about 9.0 kb was recovered. Then, 0.1 .mu.g of the EcoRI-MaeIII fragment (about 0.43 kb) of pKM796H1 or pKM750H1, as obtained above, 0.1 .mu.g of the EcoRI-ApaI fragment (about 9.0 kb) of pChi641HAM1, as obtained above, and 0.3 .mu.g of a synthetic DNA having the base sequence shown in SEQ ID NO:12 were dissolved in a total of 20 .mu.l of T4 ligase buffer, 350 units of T4 ligase was further added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101. In this way, the plasmids pChi796HM1 and pChi750HM1, shown in FIG. 6, were obtained.
Then, the .beta.-globin 3' splicing signal was introduced into the plasmids pChi796HM1 and pChi750HM1 by the method described below to construct KM796- and KM-750-derived chimeric human antibody H chain expression vectors (FIG. 7).
Three .mu.g of pChi796HM1 or pChi750HM1 were added to 30 .mu.l of 33 mM Tris-acetate buffer (pH 7.9) containing 10 mM magnesium acetate, 66 mM potassium acetate, 0.5 mM DTT and 0.01% bovine serum albumin (hereinafter, "BSA"). Ten units of XhoI and 10 units of KpnI were also added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 3.4 kb was recovered. Then, 3 .mu.g of pAGE148 obtained in (2) was added to 30 .mu.l of 33 mM Tris-acetate buffer (pH 7.9) containing 10 mM magnesium acetate, 66 mM potassium acetate, 0.5 mM DTT and 0.01% BSA; 10 units of XhoI and 10 units of KpnI were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 8.7 kb was recovered. Then, 0.1 .mu.g of the XhoI-KpnI fragment of pChi796HM1 or pKM750HM1 and 0.1 .mu.g of the XhoI-KpnI fragment of pAGE148 were dissolved in a total of 20 .mu.l of T4 ligase buffer, 350 units of T4 ligase was further added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101. The plasmids pChi796HMS1 and pChi750HMS1 shown in FIG. 7 were thus obtained.
(4) Construction of KM-796- and KM-750-derived chimeric human antibody L chain expression vectors
First, the cDNA coding for the antibody variable region in the plasmid pKM796L1 or PKM750L1 was excised by cleavage at the 5'-terminal EcoRI site and the Af1III site near the 3' end of said cDNA and joined, together with a synthetic DNA having the base sequence shown in SEQ ID NO:13, to the chimeric human antibody L chain expression vector pChiIgLA1, as follows (FIG. 8).
Three .mu.g of pKM796L1 or pKM750L1 were added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT. Further, 10 units of EcoRI and 10 units of Af1III were added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 0.39 kb was recovered. Then, 3 .mu.g of pChiIgLA1 obtained in Reference Example 1 was added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of EcoRV were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1 .mu.g of a DNA fragment of about 8.6 kb was recovered.
Then, 0.1 .mu.g of the EcoRI-Af1III fragment of pKM796L1 or pKM750L1, as obtained above, 0.1 .mu.g of the EcoRI-EcoRV fragment of pChiIgLA1, as obtained above, and 0.3 .mu.g of a synthetic DNA, having the base sequence shown in SEQ ID NO:13, were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was further added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101. In this way, the plasmids pChi796LI1 and pChi750LI1 shown in FIG. 8 were obtained.
Then, the Moloney mouse leukemia virus terminal repeat promoter/enhancer was introduced into the plasmids pChi796LI1 and pChi750LI1 in the following manner (FIG. 9).
Three .mu.g of pChi796LI1 and pChi750LI1 were added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT. Further, 10 units of EcoRI and 10 units of XhoI were added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 8.2 kb was recovered Then, 3 .mu.g of the chimric human antibody H chain expression vector pChi641HAM1 obtained in Reference Example 2 was added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of XhoI were further added, and digestion was carried out at 37.degree.0 C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 0.6 kb was recovered.
Then, 0.1 .mu.g of the EcoRI-XhoI fragment of pChi796LI1 or pKM750LI1 as obtained above and 0.1 .mu.g of the EcoRI-XhoI fragment of pChi641HAM1 as obtained above were dissolved in a total of 20 .mu.l of T4 ligase buffer, 350 units of T4 ligase was further added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101. In this way, the plasmids pChi796LM1 and pChi750LM1 shown in FIG. 9 were obtained.
Then, the .beta.-globin 3' splicing signal was introduced into the plasmids pChi796LM1 and pChi750LM1 in the manner mentioned below to construct KM-796- and KM-750-derived chimeric human antibody L chain expression vectors (FIG. 10).
Three .mu.g of pChi796LM1 or pChi750LM1 were added to 30 .mu.l of 33 mM Tris-acetate buffer (pH 7.9) containing 10 mM magnesium acetate, 66 mM potassium acetate, 0.5 mM DTT and 0.01% BSA. Further, 10 units of XhoI and 10 units of KpnI were added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 2.0 kb was recovered. Then, 3 .mu.g of pAGE148 obtained in (2) was added to 30 .mu.l of 33 mM Tris-acetate buffer (pH 7.9) containing 10 mM magnesium acetate, 66 mM potassium acetate, 0.5 mM DTT and 0.0% BSA; 10 units of XhoI and 10 units of KpnI were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 8.7 kb was recovered. Then 0.1 .mu.g of the XhoI-KpnI fragment of pChi796LM1 or pKM750LM1 as obtained above and 0.1 .mu.g of the XhoI-KpnI fragment of pAGE148 were dissolved in a total of 20 .mu.l of T4 ligase buffer, 350 units of T4 ligase was further added, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101. In this way, the plasmids pChi796LMS1 and pChi750LMS1 shown in FIG. 10 were obtained.
8. Construction of KM-796- and KM-750-Derived Chimeric Human Antibody H Chain and L Chain Tandem Expression Vectors
Tandem expression vectors containing the chimeric human antibody H chain-encoding cDNA and L chain-encoding cDNA on one and the same vector were constructed (FIG. 11 and FIG. 12).
Three .mu.g of pChi796HMS1 or pChi750HMS1, obtained in Paragraph 7, were added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT. Further, 10 units of MluI and 10 units of SalI were added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis. In each case, about 0.3 .mu.g of a DNA fragment of about 5.9 kb was recovered. Then, 2 .mu.g of pAGE107 described in EP-A-0 405 285 was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT; 10 units of MluI and 10 units of SalI were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.2 .mu.g of a DNA fragment of about 3.55 kb was recovered. Then, 0.1 .mu.g of the MluI-SalI fragment of pChi796HMS1 or pChi750HMS1 and 0.1 .mu.g of the MluI-SalI fragment of pAGE107 were dissolved in a total of 20 .mu.l of T4 ligase buffer, 350 units of T4 ligase was added, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 to give the plasmid pChi796H107 or pChi750H107 shown in FIG. 11.
Then, 3 .mu.g of pChi796H107 or pChi750H107 was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT, 10 units of ClaI was further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation. The precipitate was dissolved in 20 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the mixture was incubated at 22.degree. C. for 30 minutes for rendering the cohesive ends formed upon ClaI digestion blunt-ended. The reaction mixture was further subjected to phenol-chloroform extraction and then to ethanol precipitation. To the precipitate were added 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT, and 10 units of MluI. Digestion was carried out at 37.degree. C. for 4 hours and the reaction mixture was fractionated by agarose gel electrophoresis. In each case, about 0.3 .mu.g of a DNA fragment of about 7.5 kb was recovered. Then, 3 .mu.g of pChi796LMS1 or pChi750LMS1 was added to 30 .mu.l of 20 mM Tris-hydrochloride buffer (pH 8.5) containing 10 mM magnesium chloride, 100 mM potassium chloride and 1 mM DTT, 10 units of XhoI was further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation. The precipitate was dissolved in 20 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the mixture was incubated at 22.degree. C. for 30 minutes for rendering the cohesive ends formed upon XhoI digestion blunt-ended. The reaction mixture was further subjected to phenol-chloroform extraction and then to ethanol precipitation. To the precipitate was added 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT as well as 10 units of MluI. Digestion was carried out at 37.degree. C. for 4 hours and the reaction mixture was fractionated by agarose gel electrophoresis. In each case, about 0.3 .mu.g of a DNA fragment of about 9.3 kb was recovered. Then, 0.1 .mu.g of the MluI-ClaI fragment of pChi796H107 or pChi750H107, as obtained above, and 0.1 .mu.g of the MluI-XhoI fragment of pChi796LMS1 or pChi750LMS1, as obtained above, were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was further added, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101, and the plasmid pChi796HL1 or pChi750HL1 shown in FIG. 12 was obtained.
Construction of a KM-603-Derived Chimeric Human Antibody H Chain Expression Vector
First, the antibody variable region-encoding cDNA of the plasmid pKM603H1 was excised by cleavage at the 5'terminal EcoRI site and the StyI site near the 3' end of said cDNA and joined to the chimeric human antibody H chain expression vector pChi641HAM1 together with a synthetic DNA having the base sequence shown in SEQ ID NO:14 in the following manner (FIG. 13).
Three .mu.g of pKM603H1 obtained in Paragraph 5 were added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, followed by further addition of 10 units of EcoRI and 10 units of StyI. Digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a 0.4-kb DNA fragment was recovered. Then, 3 .mu.g of pChi641HAM1, obtained in Reference Example 2, was added to 30 .mu.l of 10 mM Tris-hydrochloride (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of ApaI were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1.0 .mu.g of a DNA fragment of about 9.0 kb was recovered. Then, 0.1 .mu.g of the EcoRI-StyI fragment (about 0.4 kb) of pKM603H1, as obtained above, and 0.1 .mu.g of the EcoRI-ApaI fragment (about 9.0 kb) of pChi641HAM1, as obtained above, were dissolved, together with 0.3 .mu.g of a synthetic DNA having the base sequence shown in SEQ ID NO:14, in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was added to the solution, and ligation was effected at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pChi603HM1 shown in FIG. 13 was obtained.
Then, a KM-603-derived chimeric human antibody H chain expression vector was constructed by introducing the .beta.-globin 3' splicing signal into the plasmid pChi603HM1 in the following manner (FIG. 14).
Three .mu.g of pChi603HM1 obtained above were added to 30 .mu.l of 33 mM Tris-acetate buffer (pH 7.9) containing 10 mM magnesium acetate, 66 mM potassium acetate, 0.5 mM DTT and 0.01% BSA. Further, 10 units of XhoI and 10 units of KpnI were added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 3.3 kb was recovered.
Then, 3 .mu.g of pAGE148 obtained in Paragraph 7 (2) was added to 30 .mu.l of 33 mM Tris-acetate buffer (pH 7.9) containing 10 mM magnesium acetate, 66 mM sodium acetate, 0.5 mM DTT and 0.01% BSA; 10 units of XhoI and 10 units of KpnI were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 8.7 kb was recovered. Then, 0.1 .mu.g of the XhoI-KpnI fragment of pChi603HM1, as obtained above, and 0.1 .mu.g of the XhoI-KpnI fragment of pAGE148, as obtained above, were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pChi603HMS1 shown in FIG. 14 was obtained.
10. Construction of a KM-603-Derived Chimeric Human Antibody L Chain Expression Vector
First, the antibody variable region cDNA in the plasmid pKM603L1 was excised by cleavage at the 5' terminal EcoRI site and the Af1III site near the 3' end and joined to the chimeric human antibody L chain expression vector pChiIgLA1 together with a synthetic DNA having the base sequence defined by SEQ ID NO:15 (FIG. 15).
Thus, 3 .mu.g of pKM603L1 obtained in Paragraph 5 was added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of Af1III were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 0.4 kb was recovered. Then, 3 .mu.g of pChiIgLA1 obtained in Reference Example 1 was added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of EcoRV were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1 .mu.g of a DNA fragment of about 8.6 kb was recovered. Then, 0.1 .mu.g of the EcoRI-Af1III fragment of pKM603L1, as obtained above, 0.1 .mu.g of the EcoRI-EcoRV fragment of pChiIgLA1, as obtained above, and 0.3 .mu.g of a synthetic DNA, having the base sequence defined by SEQ ID NO:15, were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pChi603LI1 shown in FIG. 15 was obtained.
Then, the Moloney mouse leukemia virus terminal repeat promoter/enhancer was introduced into the plasmid pChi603LI1 in the following manner (FIG. 16).
Thus, 3 .mu.g of pChi603LI1 obtained above was added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of XhoI were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 8.3 kb was recovered. Then, 3 .mu.g of pChi641HAM1 obtained in Reference Example 2 was added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of XhoI were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 0.6 kb was recovered. Then, 0.1 .mu.g of the EcoRI-XhoI fragment of pChi603LI1, as obtained above, and 0.1 .mu.g of the EcoRI-XhoI fragment of pChi641HAM1, as obtained above, were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was added to the solution, and ligation was effected at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Eschrichia coli HB101 to give the plasmid pChi603LM1 shown in FIG. 16.
A KM-603-derived chimeric human antibody L chain expression vector was then constructed by introducing the .beta.-globin 3' splicing signal into the plasmid pChi603LM1, as follows (FIG. 17).
Thus, 3 .mu.g of pChi603LM1 obtained above was added to 30 .mu.l of 33 mM Tris-acetate buffer (pH 7.9) containing 10 mM magnesium acetate, 66 mM potassium acetate, 0.5 mM DTT and 0.01% BSA, 10 units of XhoI and 10 units of KpnI were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 2.0 kb was recovered. Then, 3 .mu.g of pAGE148 obtained in Paragraph 7 (2) was added to 30 .mu.l of 33 mM Tris-acetate buffer (pH 7.9) containing 10 mM magnesium acetate, 66 mM potassium acetate, 0.5 mM DTT and 0.01% BSA, 10 units of XhoI and 10 units of KpnI were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a DNA fragment of about 8.7 kb was recovered. Then, 0.1 .mu.g of the XhoI-KDnI fragment of pChi603LM1, as obtained above, and 0.1 .mu.g of the XhoI-KpnI fragment of pAGE148, as obtained above, were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 to give the plasmid pChi603LMS1 shown in FIG. 17.
11. Expression of the KM-796- and KM-750-Derived Chimeric Human Anti-GM2 Antibody in YB2/0 Cells
The plasmids were introduced into YB2/0 cells by the electroporation method of Miyaji et al. �Cytotechnbology, 3, 133-140 (1990)!.
After introduction of 4 .mu.g of pChi750HL1 or pChi796HL1 obtained in Paragraph 8 into 4.times.10.sup.6 YB2/0 (ATCC CRL1581) cells, the cells were suspended in 40 ml of RPMI-1640-FCS(10) �RPMI1640 medium (Nissui Pharmaceutical) containing 10% of FCS, 1/40 volume of 7.5% NaHCO.sub.3, 3% of 200 mM L-glutamine solution (Gibco) and 0.5% of penicillin-streptomycin solution (Gibco; containing 5,000 units/ml penicillin and 5,000 .mu.g/ml streptomycin)!, and the suspension was distributed in 200-.mu.l portions into wells of 96-well microtiter plates. After 24 hours of incubation at 37.degree. C. in a CO.sub.2 incubator, G418 (Gibco) was added to a concentration of 0.5 mg/ml and then incubation was continued for 1 to 2 weeks. Transformant colonies appeared, the culture fluid was recovered from each well in which the cells had grown to confluence and an enzyme-linked immunosorbent assay (ELISA) was conducted for anti-GM.sub.2 chimeric human antibody activity measurement.
Enzyme-Linked Immunosorbent Assay (ELISA)
In a solution of 5 ng of phosphatidylcholine (Sigma) and 2.5 ng of cholesterol (Sigma) in 2 ml of ethanol was dissolved 2 ng of GM.sub.2 (N-acetyl-GM.sub.2 ; Boehringer Mannheim) or some other ganglioside. The solution or dilutions thereof were respectively distributed in 20-.mu.l portions into wells of 96-well microtiter plates (Greiner) and, after air drying, blocking was effected with PBS containing 1% BSA. Each culture supernatant for each transformant, each purified mouse monoclonal antibody solution and each purified chimeric human antibody solution were distributed in 50- to 100-.mu.l portions into the wells and the reaction was allowed to proceed at room temperature for 1 to 2 hours. The wells were then washed with PBS, and 50 to 100 .mu.l of peroxidase-labeled antibody were added thereto followed by reaction at room temperature for 1 to 2 hours. The wells were washed with PBS and an ABTS substrate solution �prepared by dissolving 550 mg of 2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt in 0.1M citrate buffer (pH 4.2) and adding, just prior to use, hydrogen peroxide to a concentration of 1 .mu.l/ml! was added in 50- to 100-.mu.l portions to each well for color development, followed by OD.sub.415 measurement.
The clone showing the highest activity in ELISA among the clones obtained gave a chimeric human anti-GM.sub.2 antibody content of about 1.0 .mu.g/ml of culture fluid.
Cells of the clone showing the above-mentioned chimeric human anti-GM.sub.2 antibody activity were suspended in RPMI1640-FCS(10) medium containing 0.5 mg/ml G418 and 50 nM methotrexate (hereinafter, "MTX") to a concentration of 1 to 2.times.10.sup.5 cells/ml, and the suspension was distributed in 2-ml portions into wells of 24-well plates. Incubation was performed at 37.degree. C. in a CO.sub.2 incubator for 1 to 2 weeks to induce 50 nM MTX-resistant clones. At the time of confluence, the chimeric human anti-GM.sub.2 antibody activity in each culture fluid was determined by ELISA. The 50 nM MTX-resistance clone showing the highest activity among the clones obtained showed a chimeric human anti-GM.sub.2 antibody content of about 5.0 .mu.g/ml.
Cells of the above 50 nM MTX-resistant clone were suspended in RPMI1640-FCS(10) medium containing 0.5 mg/ml G418 and 200 nM MTX to a concentration of 1 to 2.times.10.sup.5 cells/ml, and the suspension was distributed in 2-ml portions into wells of 24-well plates. Incubation was carried out at 37.degree. C. in a CO.sub.2 incubator for 1 to 2 weeks to induce 200 nM MTX-resistant clones. At the time of confluence, each culture fluid was assayed for chimeric human anti-GM.sub.2 antibody activity by ELISA. The 200 nM MTX-resistant clone showing the highest activity among the clones obtained had a chimeric human anti-GM.sub.2 antibody content of about 10 .mu.g/ml. The 200 nM MTX-resistant clones obtained from pChi750HL1 and pChi796HL1 were named transformants "KM966" (KM-796-derived chimeric human antibody KM966-producing strain) and "KM967" (KM-750-derived chimeric human antibody KM967-producing strain), respectively.
The following SDS-polyacrylamide gel electrophoresis (SDS-PAGE) confirmed that the above transformants KM966 and KM967 express the respective chimeric human anti-GM.sub.2 antibodies.
The transformants KM966 and KM967 were each suspended in GIT medium (Nippon Pharmaceutical) containing 0.5 mg/ml G418 and 200 nM MTX to a concentration of 1 to 2.times.10.sup.5 cells/ml. Each suspension was distributed in 100-ml portions into 175 cm.sup.2 flasks (Greiner). Cultivation was performed at 37.degree. C. in a CO.sub.2 incubator for 5 to 7 days. At the time of confluence, the culture fluid was recovered. Treatment of about 1 liter of the culture fluid with Affi-Gel Protein A MAPS-II kit (Bio-Rad) gave about 5 mg of a purified chimeric human anti-GM.sub.2 antibody for each transformant. About 2 .mu.g of the purified chimeric human anti-GM.sub.2 antibody KM966 or KM967 was electrophoresed by the conventional method �Laemmli: Nature, 227, 680 (1970)! for molecular weight checking. The results are shown in FIG. 18. As shown in FIG. 18, both KM966 and KM967 gave an antibody H chain molecular weight of about 50 kilodaltons and an antibody L chain molecular weight of about 25 kilodaltons under reducing conditions, indicating the correctness in molecular weight of the H chain and L chain expressed. For each of KM966 and KM967, the molecular weight of the chimeric human antibody under nonreducing conditions was about 150 kilodaltons, indicating that the antibody expressed was composed of two H chains and two L chains and was correct in size.
12. Expression of KM-603-Derived Chimeric Human Anti-GM.sub.2 Antibodies in SP2/0 Cells
A 2-.mu.g portion of the plasmid pChi603HMS1 or pChi603LMS1 obtained in Paragraph 9 was introduced into 4.times.10.sup.6 cells of YB2/0 (ATCC CRL1581) by electroporation in the same manner in Paragraph 11. The cells were suspended in 40 ml of RPMI1640-FCS(10) and the suspension was distributed in 200-.mu.l portions into wells of 96-well microtiter plates. After 24 hours of incubation in a CO.sub.2 incubator at 37.degree. C., G418 (Gibco) was added to a concentration of 0.5 mg/ml and incubation was continued for 1 to 2 weeks. Transformant colonies appeared. The culture fluid was recovered from confluent wells and the chimeric human anti-GM.sub.2 antibody activity was measured by ELISA as described above. The clone showing the highest chimeric human anti-GM.sub.2 antibody activity among the clones obtained gave a chimeric human anti-GM.sub.2 antibody content of about 0.1 .mu.g/ml of culture fluid.
Cells of the clone showing the above-mentioned chimeric human anti-GM.sub.2 antibody activity were suspended in RPMI1640-FCS(10) medium containing 0.5 mg/ml G418 and 50 nM MTX to a concentration of 1 to 2.times.10.sup.5 cells/ml and the suspension was distributed in 2-ml portions into wells of 24-well plates. Clones resistant to 50 nM MTX were induced by incubating in a CO.sub.2 incubator at 37.degree. C. for 2 to 3 weeks. When confluence was attained, the culture fluids were subjected to ELISA for chimeric human anti-GM.sub.2 antibody activity measurement. Among the 50 nM MTX-resistant clones obtained, the clone showing the highest activity gave a chimeric human anti-GM.sub.2 antibody content of about 0.3 .mu.g/ml of culture fluid.
Cells of the above 50 nM MTX-resistant clone were suspended in RPMI1640-FCS(10) medium containing 0.5 mg/ml G418 and 200 nM MTX to a concentration of 1 to 2.times.10.sup.5 cells/ml and the suspensions as distributed in 2-ml portions into well of 24-well plates. Clones resistant to 200 nM MTX were induced by following incubation in a CO.sub.2 incubator at 37.degree. C. for 2 to 3 weeks. When confluence was attained, the chimeric human anti-GM.sub.2 antibody activity in the culture fluid was measured by ELISA. Among the 200 nM MTX-resistant clones obtained, the clone showing the highest activity gave a chimeric human anti-GM.sub.2 antibody content of about 0.5 .mu.g/ml of culture fluid.
Cells of the above 200 nM MTX-resistant clone were suspended in RPMI1640-FCS(10) medium containing 0.5 mg/ml G418 and 500 nM MTX to a concentration of 1 to 2.times.10.sup.5 cells/ml and the suspension was distributed in 2-ml portions into well of 24-well plates. Clones resistant to 500 nM MTX were induced following incubation in a CO.sub.2 incubator at 37.degree. C. for 1 to 2 weeks. When confluence was attained, the chimeric human anti-GM.sub.2 antibody activity in the culture fluid was determined by ELISA. Among the 500 nM MTX-resistant clones obtained, the one showing the highest activity gave a chimeric human anti-GM.sub.2 antibody content of about 1.0 .mu.g/ml of culture fluid. This 500 nM MTX-resistant clone was named "transformant KM968".
The following SDS-PAGE confirmed the expression of a chimeric human anti-GM.sub.2 antibody in the above transformant KM968.
Cells of the transformant KM968 were suspended in GIT medium (Nippon Pharmaceutical) containing 0.5 mg/ml G418 and 500 nM MTX to a concentration of 1 to 2.times.10.sup.5 cells/ml and the suspension was distributed in 100-ml portions into 175 cm.sup.2 flasks (Greiner). Cultivation was conducted in a CO.sub.2 incubator at 37.degree. C. for 5 to 7 days and, when confluence was attained, the culture fluid was recovered. Treatment of about 3.0 liters of the culture fluid with Affi-Gel Protein A MAPS-II kit (Bio-Rad) gave about 1 mg of a purified chimeric human anti-GM.sub.2 antibody. About 2 .mu.g of this purified chimeric human anti-GM.sub.2 antibody KM968 was electrophoresed by the conventional method �Laemmli: Nature, 227, 680 (1970)! for molecular weight checking. The results are shown in FIG. 19. Under reducing conditions, the molecular weight of the antibody H chain was about 50 kilodaltons and the molecular weight of the antibody L chain was about 25 kilodaltons, thus confirming the expression of the H chain and L chain having the correct molecular weight. Under nonreducing conditions, the molecular weight of the chimeric human antibody was about 150 kilodaltons, confirming that the antibody expressed was composed of two H chains and two L chains and was correct in size.
13. Reaction Specificity of the Chimeric Human Anti-GM.sub.2 Antibodies
The reactivities of the chimeric anti-GM.sub.2 antibodies with ganglioside GM.sub.1, N-acetyl-GM.sub.2 (Boehringer Mannheim), N-glycolyl-GM.sub.2, N-acetyl-GM.sub.3, N-glycolyl-GM.sub.3, GD.sub.1a, GD.sub.1b (Iatron), GD.sub.2, GD.sub.3 (Iatron) and GQ.sub.1b (Iatron) were examined by the technique of ELISA. The results are shown below in Table 1. GM.sub.1 and GD.sub.1a were purified from the bovine brain, N-glycolyl-GM.sub.2 and N-glycolyl-GM.sub.3 from the mouse liver, N-acetyl-GM.sub.3 from canine erythrocytes, and GD.sub.2 from the cultured cell line IMR32 (ATCC CCL127), by a known method �J. Biol. Chem., 263, 10915 (1988)!.
As shown in Table 1, it was confirmed that the chimeric human anti-GM.sub.2 antibodies KM966 and KM967 specifically react with GM.sub.2. The reactivity of KM966 was greater than that of KM967, however. On the contrary, KM968 (KM-603-derived chimeric human antibody) did not show any reactivity for GM.sub.2.
TABLE 1______________________________________ Binding activity of antibody (OD.sub.415)Ganglioside KM966 (5 .mu.g/ml) KM967 (5 .mu.g/ml)______________________________________GM.sub.1 0.105 0.000N-Acetyl-GM.sub.2 0.870 0.423N-Glycolyl-GM.sub.2 0.774 0.065N-Acetyl-GM.sub.3 0.002 0.000N-Glycolyl-GM.sub.3 0.122 0.001GD.sub.1a 0.004 0.000GD.sub.1b 0.002 0.000GD.sub.2 0.095 0.001GD.sub.3 0.004 0.000GQ.sub.1b 0.005 0.000______________________________________
14. Reactivities of the Chimeric Human Anti-GM.sub.2 Antibodies KM966 and KM967 With Cancer Cells (Fluorescent Antibody Technique)
Suspended in PBS were 1.times.10.sup.6 cells of cultured human lung small cell carcinoma cell line QC90 �Cancer Res., 49, 2683 (1989)!, NCI-H69 (ATCC HTB119), NCI-H128 (ATCC HTB120), SBC-1 (JCRB 0816), SBC-2 (JCRB 0817), SBC-3 (JCRB 0818), SBC-5 (JCRB 0819), RERF-LC-MA (JCRB 0812), Lu-134-A-H (JCRB 0235), Lu-139 (RCB 469), Lu-130 (RCB 465), Lu-135 (RCB 468), Lu-134-B (RCB 467), Lu-140 (RCB 470), PC-6 �Naito et al.: Gann to Kagaku Ryoho (Cancer and Chemotherapy), 5 (suppl.), 89 (1978)!, cultured human lung squamous carcinoma cell line PC-1 �Naito et al.: Gann to Kagaku Ryoho, 5 (suppl.), 89 (1978)!, PC-10 �Naito et al.: Gann to Kagaku Ryoho, 5 (suppl.), 89 (1978)!, Colol6 �Moor et al.: Cancer Res., 35, 2684 (1975)!, Calu-1 (ATCC HTB54), SK-LC-4 �Proc. Natl. Acad. Sci. U.S.A., 85, 4441 (1988)!, cultured human lung adenocarcinoma cell line PC-7 �Hayata et al.: Hito Gansaibo no Baiyo (Human Cancer Cell Culture), 131 (1975)!, PC-9 �Kinjo et al.: Brit. J. Cancer, 39, 15 (1979)!, PC-12 (ATCC CRL1721), RERF-LC-MS (JCRB 0081), HLC-1 (RCB 083), cultured human lung large cell carcinoma cell line PC-13 �Oboshi et al.: Tanpakushitsu, Kakusan, Koso (Protein, Nucleic Acid, Enzyme), 23, 697 (1978)!, Lu65 (JCRB 0079), CALU-6 (ATCC HTB56), SK-LC-6 �Proc. Natl. Acad. Sci. U.S.A., 85, 4441 (1988)!, cultured human neuroblastoma cell line YT-nu �Ishikawa et al.: Acta Path. Jap., 27, 697 (1977)!, NAGAI �Ishikawa et al.: Acta Path. Jap., 29, 289 (1979)!, NB-1 �Ishikawa et al.: Acta Path. Jap., 27, 697 (1977)!, IMR32 (ATCC CCL127), GOTO (JCRB 0612), NB-9 (RCB 477), SK-N-MC (ATCC HTB10), cultured human brain tumor (glioma) cell line SK-MG-4 �EMBO J., 6, 2939 (1987)!, A172 (ATCC CRL1620), T98G (ATCC CRL1690), U-118MG (ATCC HTB15), cultured human leukemia cell line HSB-2 (ATCC CCL120.1), ATN-1, U-937 (ATCC CRL1593), HPB-ALL �Oboshi et al.: Tanpakushitsu, Kakusan, Koso, 23, 697 (1978)!, CCRF-SB (ATCC CCL120), KOPN-K �Hanei et al.: Haigan (Lung Cancer), 25, 524 (1985)!, TYH �Haranaka et al.: Int. J. Cancer, 36, 313 (1985)!, MOLT-3 (ATCC CRL1552), CCRF-CEM (ATCC CCL119), TALL-1 (JCRB 0086), NALL-1 �Oboshi et al.: Tanpakushitsu, Kakusan, Koso, 23, 697 (1978), CCRF-SB (JCRB 0032), THP-1 (ATCC TIB202), HEL92-1-7 (ATCC TIB180), cultured human maligant melanoma cell line C24.cndot.32 (EP-A-0 493686), KHm-3/P �J. Natl. Cancer Inst., 59, 775 (1977)! or G361 (ATCC CRL1424). The suspension was placed in a microtube (Tref) and centrifuged (3,000 rpm, 2 minutes) to wash the cells, 50 .mu.l of KM966 or KM967 (50 .mu.g/ml) was added, the mixture was stirred, and the reaction was allowed to proceed at 4.degree. C. for 1 hour. Then, the cells were washed three times by centrifugation with PBS, 20 .mu.l of fluorescein isocyanate-labeled protein A (30-fold dilution; Boehringer Mannheim Yamanouchi) was added and, after stirring, the reaction was allowed to proceed at 4.degree. C. for 1 hour. Then, the cells were washed three times by centrifugation with PBS, then suspended in PBS and subjected to analysis using flow cytometer EPICS Elite (Coulter). In a control run, the same procedure as described above was followed without adding the chimeric human antibody. The results thus obtained are shown in Table 2. The chimeric human antibody KM966 reacted with 9 (NCI-H-128, SBC-1, SBC-3, SBC-5, Lu-139, Lu-130, Lu-135, Lu-134-B and Lu-140) of the 14 lung small cell carcinoma cell lines, 2 (PC-10 and Calu-1) of the 5 lung squamous carcinoma cell lines, 2 (PC-9 and RERF-LC-MS) of the 5 lung adenocarcinoma cell lines, 2 (PC-13 and SK-LC-6) of the 4 lung large cell carcinoma cell lines, 7 (YT-nu, NAGAI, NB-1, IMR32, GOTO, NB-9 and SK-N-MC) of the 7 neuroblastoma cell lines and 4 (SK-MG-4, A172, T98G and U-118MG) of the 4 brain tumor (glioma) cell lines. On the other hand, the chimeric human antibody KM967 did not react with any of the cultured cell lines. The above results indicate that the chimeric human antibody KM966 is useful in the diagnosis and treatment of brain tumors, peripheral nervous system tumors and lung cancer, among others.
TABLE 2______________________________________ KM966 (%) KM967 (%)Cell line (50 .mu.g/ml) (50 .mu.g/ml)______________________________________Lung small cell carcinoma 9/14 (64) 0/14 (0)Lung squamous cell 2/5 (40) 0/5 (0)carcinomaLung adenocarcinoma 2/5 (40) 0/5 (0)Lung large cell carcinoma 2/4 (50) 0/4 (0)Neuroblastoma 7/7 (100) 0/7 (0)Brain tumor (glioma) 4/4 (100) 0/4 (0)Leukemia 0/14 (0) 0/14 (0)Malignant melanoma 0/3 (0) 0/3 (0)______________________________________
15. In Vitro Antitumor Activity of the Chimeric Human Anti-GM.sub.2 Antibody KM966: Complement Dependent Cytotoxicity (CDC)
(1) Preparation of target cells
The target cells SBC-3, Lu-135, PC-10, RERF-LC-MS, PC-13, NAGAI, GOTO or A172, cultured in RPMI1640 medium supplemented with 10% FCS, were adjusted to a cell concentration of 5.times.10.sup.6 cells/ml, Na.sub.2.sup.51 CrO.sub.4 was added to a concentration of 100 .mu.Ci/5.times.10.sup.6 cells, then the reaction was allowed to proceed at 37.degree. C. for 1 hours, and the cells were washed three times with the medium. The cells were then allowed to stand in the medium at 4.degree. C. for 30 minutes for spontaneous dissociation and then, after centrifugation, the medium was added to adjust the cell concentration to 1.times.10.sup.6 cells/ml.
(2) Preparation of the complement
Sera from three healthy subjects were combined and used as a complement source.
(3) CDC activity measurement
The chimeric human anti-GM.sub.2 antibody KM966 or mouse anti-GM.sub.2 antibody KM696 (FERM BP-3337) was added to wells of 96-well U-bottom plates within the final concentration range of 0.5 to 50 .mu.g/ml and then 5.times.10.sup.4 cells/well of the target cells prepared in (1) were added. The reaction was allowed to proceed at room temperature for 30 minutes. After centrifugation, the supernatants were discarded, 150 .mu.l of the human serum obtained in (2) was added to each well (final concentration 15% v/v), and the reaction was allowed to proceed at 37.degree. C. for 1 hour. After centrifugation, the amount of .sup.51 Cr in each supernatant was determined using a gamma counter. The amount of spontaneously dissociated .sup.51 Cr was determined by adding to the target cells the medium alone in lieu of the antibody and complement solutions and measuring the amount of .sup.51 Cr in the supernatant in the same manner as mentioned above. The total amount of dissociated .sup.51 Cr was determined by adding to the target cells 5 N sodium hydroxide in lieu of the antibody and complement solutions and measuring the amount of 51Cr in the supernatant in the same manner as mentioned above. The CDC activity was calculated as follows: ##EQU1##
The results thus obtained are shown in FIGS. 20 to 23. It was shown that the chimeric human antibody KM966 show CDC activity against all the cells tested.
16. In Vitro Antitumor Activity of the Chimeric Human Anti-GM.sub.2 Antibody KM966: Antibody Dependent Cell Mediated Cytotoxicity (ADCC)
(1) Preparation of target cells
The target cells SBC-3, Lu-135, PC-10, RERF-LC-MS, PC-13, NAGAI, GOTO or A172, cultured in RPMI1640 medium supplemented with 10% FCS, were adjusted to a cell concentration of 1.times.10.sup.6 cells/ml, Na.sub.2.sup.51 CrO.sub.4 was added to a concentration of 50 .mu.Ci/1.times.10.sup.6 cells, then the reaction was allowed to proceed at 37.degree. C. for 1 hour, and the cells were washed three times with the medium. The cells were then allowed to stand in the medium at 4.degree. C. for 30 minutes for spontaneous dissociation and then, after centrifugation, the medium was added to adjust the cell concentration to 2.times.10.sup.5 cells/ml.
(2) Preparation of effector cells
Human venous blood (25 ml) was collected, 0.5 ml of heparin sodium (Takeda Chemical Industries; 1,000 units/ml) was added, and the mixture was gently stirred. This mixture was centrifuged (1,500 to 1,800 g, 30 minutes) using Polymorphprep (Nycomed Pharma AS), the lymphocyte layer was separated and washed three times by centrifugation with RPMI1640 medium (15,00 to 1,800 g, 15 minutes), and the cells were suspended in RPMI1640 medium supplemented with 10% FCS (5.times.10.sup.6 cells/ml) for use as effector cells.
(3) ADCC activity measurement
The chimeric human anti-GM.sub.2 antibody KM966 or mouse anti-GM.sub.2 antibody KM696 were added to wells of 96-well U-bottom plates within the final concentration range of 0.05 to 5 .mu.g/ml and then 50 .mu.l (1.times.10.sup.4 cells/well) of the target cell suspension prepared in (1) and 100 .mu.l (5.times.10.sup.5 cells/well) of the effector cell suspension prepared in (2) were added to each well (the ratio between the effector cells and target cells being 50:1). The reaction was allowed to proceed at 37.degree. C. for 4 hours and, after centrifugation, the amount of .sup.51 Cr in each supernatant was measured using a gamma counter. The amount of spontaneously dissociated .sup.51 Cr was determined by adding to the target cells the medium alone in lieu of the antibody and effector cells and measuring the amount of .sup.51 Cr in the supernatant in the same manner as mentioned above. The total amount of dissociated .sup.51 Cr was determined by adding to the target cells 5N sodium hydroxide in lieu of the antibody and effector cells and measuring the amount of .sup.51 Cr in the supernatant in the same manner as mentioned above. The ADCC activity was calculated as follows: ##EQU2##
The results thus obtained are shown in FIGS. 24 to 27. The chimeric antibody KM966 showed ADCC activity against all the cells whereas the mouse anti-GM.sub.2 antibody KM696 showed no or low ADCC activity. The above results indicate that the chimeric human antibody KM966 is more effective in the treatment of human cancer than the mouse antibody KM-696.
REFERENCE EXAMPLE 1
Construction of the Vector pChiIgLA1 for Chimeric Human Antibody L Chain Expression
1. Isolation of the KM50 Cell-Derived Immunoglobulin H Chain Promoter and Enhancer Genes
(1) Preparation of chromosomal DNAs from KM50 cells, P3U1 cells and rat kidney
Chromosal DNAs were prepared by the conventional method �Maniatis et al. (ed.): Molecular Cloning, 1989, p. 9.16!, as follows.
KM50 cells (1.2.times.10.sup.8 cells), P3U1 cells (ATCC CRL1597) (2.times.10.sup.8 cells) and a rat kidney sample (frozen at -80.degree. C. and then smashed to a sufficient extent using a wooden hammer) (1.6 g) were suspended in 2 ml of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 150 mM sodium chloride and 10 mM ethylenediaminetetraacetic acid disodium salt (hereinafter, "EDTA"), 0.8 mg of proteinase K (Sigma) and 10 mg of sodium lauryl sulfate (hereinafter, "SDS"), were added to each suspension, and the suspension was incubated at 37.degree. C. for 10 hours. Then, each mixture was extracted once with an equal volume of phenol, twice with an equal volume of chloroform and then once with an equal volume of ether, and dialyzed for 10 hours against 10 mM Tris-hydrochloride buffer (pH 7.5) containing 1 mM EDTA. The DNA solution was recovered from the dialysis tube and ribonuclease A (Sigma) was added to the solution to a final concentration of 20 .mu.g/ml. Each resultant solution was incubated at 37.degree. C. for 6 hours for sufficient decomposition of RNA, 15 mg of SDS and 1 mg of proteinase K were then added and the mixture was incubated at 37.degree. C. for 10 hours. The mixture was then extracted twice with an equal volume of phenol, twice with an equal volume of chloroform and twice with an equal volume of ether and then dialyzed for 10 hours against 10 mM Tris-hydrochloride buffer (pH 7.5) containing 1 mM EDTA. The DNA solution was recovered from the dialysis tube for use as a chromosomal DNA sample. DNA concentration measurement in terms of the absorbance at 260 nm revealed that the yield of chromosomal DNA from 1.2.times.10.sup.8 KM50 cells was 1.6 mg, that from 2.times.10.sup.8 P3U1 cells 1.5 mg, and that from 1.6 g of rat liver 1.9 mg.
(2) Identification of the active-form immunoglobulin H chain gene in KM50 cells by Southern blotting
The KM50 cell, p3U1 cell and rat kidney chromosomal DNAs obtained in (1) (3 .mu.g each) were dissolved in 25 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 15 units of XbaI (Takara Shuzo; hereinafter the restriction enzymes used were products of Takara Shuzo) was added and incubation was carried out at 37.degree. C. for 2 hours for effecting cleavage at the XbaI sites. Each reaction mixture was subjected to agarose gel electrophoresis, then DNA transfer onto a nitrocellulose filter was effected by the method of Southern et al. �J. Mol. Biol., 98, 503 (1975)! and hybridization was carried out by the conventional method �Kameyama et al.: FEBS Letters, 244, 301-306 (1989)! using the mouse JH probe described in the last-cited reference. The KM50 cell DNA alone gave a band at a site corresponding to about 9.3 kb. Therefore, the immunoglobulin XbaI fragment DNA was considered to code for the active-form immunoglobulin H chain gene in KM50 cells. (3) Construction of a KM50 cell genomic DNA library A 60-.mu.g portion of the KM50 cell-derived chromosomal DNA obtained in (1) was dissolved in 250 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 150 units of XbaI was added, and incubation was conducted at 37.degree. C. for 2 hours for causing cleavage at the XbaI sites. The reaction mixture was fractionated by agarose gel electrophoresis and a KM50 cellderived 9.3 kb DNA fraction sample (about 2 .mu.g) was recovered using, for example, the DEAE paper method �Maniatis et al. (ed.): Molecular Cloning, 1989, p. 6.24!. Separately, 3 .mu.g of Lambda ZAP (Stratagene), for use as the vector, was dissolved in 200 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 50 units of XbaI was added, and the mixture was incubated at 37.degree. C. for 2 hours to effect cleavage at the XbaI sites. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, whereby about 3 .mu.g of DNA was recovered. This DNA was dissolved in 100 .mu.l of 100 mM Tris-hydrochloride buffer (pH 7.5), 1 unit of alkaline phosphatase (Takara Shuzo) was added, dephosphorylation was effected at the restriction enzyme cleavage ends of the vector DNA. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, whereby 2 .mu.g of DNA was recovered. This DNA was dissolved in 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 1 mM EDTA for use as a vector sample. Two tenths .mu.g of the vector DNA sample and 0.2 .mu.g of the KM50 cell-derived 9.3 kb DNA sample were dissolved in 5 .mu.l of T4 ligase buffer, 175 units of T4 ligase (Takara Shuzo) was added, and the mixture was incubated at 4.degree. C. for 3 days. A 2-.mu.l portion of this mixture was packaged into the lambda phage by the conventional method �Maniatis et al. (ed.): Molecular Cloning, 1989, p. 2.95! using Giga Pak Gold (Stratagene), and the packaging mixture was used to transfect Escherichia coli BB4 to give 200,000 phage clones. Among them, 100,000 clones were fixed on a nitrocellulose filter by the conventional method �Maniatis et al. (ed.): Molecular Cloning, 1989, p. 2.112!.
(4) Selection of a recombinant DNA containing the gene for the H chain variable region of an immunoglobulin occurring as an active form in KM50 cells (anti-human serum albumin)
From among the phage library composed of 100,000 clones, as constructed in (3), two clones firmly associable at 65.degree. C. with the .sup.32 P-labeled mouse JH probe �labeled by the method of Kameyama et al. �FEBS Letters, 44, 301-306 (1989)!! were isolated. The phage DNA was recovered from them by the conventional method �Maniatis et al. (ed.): Molecular Cloning, 1989, p. 2.118-2.169!, whereupon the 9.3 kb XbaI fragment of the KM50 cell-derived chromosomal DNA was found to have been inserted therein.
(5) Base sequence of the gene for the H chain variable region of the immunoglobulin occurring as an active form in KM50 cells (anti-human serum albumin)
For the two clones obtained in (4), restriction enzyme cleavage maps were prepared by conducting digestion using various restriction enzymes, whereby it was revealed that the same DNA fragment (9.3 kb) had been inserted therein (FIG. 28). Therefore, those portions of this 9.3 kb DNA fragment which were supposed to be coding for the rat immunoglobulin H chain promoter region and variable region were sequenced by the method of Sanger �Sanger et al.: Proc. Natl. Acad. Sci. U.S.A., 74, 5463 (1977); AMERSHAM M13 cloning and sequencing handbook!. In SEQ ID NO:16, the portion containing the octamer sequence such as ATGCAAAT and the TATA box sequence such as TTGAAAA is considered to be the immunoglobulin promoter region.
2. Construction of Heterologous Protein Expression Vectors Using the Promoter and Enhancer For the H Chain Variable Region Gene for an Immunoglobulin Occurring as an Active Form in KM50 cells (anti-human serum albumin)
(1) Construction of pKMB11
A 1-.mu.g portion of the 9.3 kb immunoglobulin H chain variable region gene fragment obtained in Paragraph 1 (5) was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units each of BglII and HindIII were added, and the mixture was incubated at 37.degree. C. for 2 hours for causing cleavage at the BglII and HindIII sites. The reaction mixture was subjected to agarose gel electrophoresis and 0.01 .mu.g of a DNA fragment containing the 0.8 kb immunoglobulin promoter was recovered. Then, 1 .mu.g of the plasmid pBR322-BglII �Kuwana et al.: FEBS Letters, 219, 360 (1987)! was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of BglII and 10 units of HindIII were added, and the mixture was incubated at 37.degree. C. for 2 hours to effect cleavage at the BglII and HindIII sites. The reaction mixture was subjected to agarose gel electrophoresis and a DNA fragment of about 4.2 kb in size was recovered. The thus-obtained pBR322-BglII-derived DNA fragment (about 4.2 kb, 0.1 .mu.g) and immunoglobulin promoter-containing DNA fragment (0.01 yg) were dissolved in 20 .mu.l of T4 ligase buffer, 175 units of T4 DNA ligase (Takara Shuzo) was added, and the mixture was incubated at 4.degree. C. for 1 day. The reaction mixture was used to transform Escherichia coli HB101 �J. Mol. Biol., 41, 459 (1969)! by the method of Scott et al. �Masaru Shigesada: Saibo Kokagu (Cell Engineering), 2, 616 (1983)! to give an Ap-resistant colony. The recombinant plasmid DNA was recovered from this colony. Plasmid pKMB11, shown in FIG. 29, was thus obtained.
(2) Construction of pKMD6
For providing an appropriate restriction enzyme site downstream from the immunoglobulin promoter, the plasmid pKMB11 constructed in (1) was digested at the NcoI site using the nuclease BAL31. Thus, 10 .mu.g of the plasmid pKMB11 was dissolved in 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM potassium chloride, 30 units of NcoI was added, and the mixture was incubated at 37.degree. C. for 2 hours to effect cleavage at the NcoI site. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the whole amount of the DNA fragment was dissolved in 100 .mu.l of BAL31 buffer (20 mM Tris-hydrochloride buffer (pH 8.0) containing 600 mM sodium chloride, 12 mM calcium chloride, 12 mM magnesium chloride and 1 mM EDTA!, 0.25 unit of BAL31 �Bethesda Research Laboratories (BRL)!! was added, and digestion was carried out at 37.degree. C. for 5 seconds. The reaction was terminated by extraction with phenol and subjected to chloroform extraction and then to ethanol precipitation, and 1 .mu.g of DNA was recovered. A 0.1-.mu.g portion of this DNA and 0.01 .mu.g of a synthetic DNA linker (SalI) were dissolved in 20 .mu.l of T4 ligase buffer, 175 units of T4 DNA ligase was added, and the mixture was incubated at 4.degree. C. for 1 day. The reaction mixture was used to transform Escherichia coli HB101 by the method of Scott et al. An Ap-resistant colony was obtained and the recombinant plasmid DNA was recovered from this colony to give the plasmid pKMD6 shown in FIG. 30. For this plasmid, the portion of BAL31 digestion was sequenced by the method of Sanger, whereupon deletion was found to the third base (303rd base in SEQ ID NO:16) toward the upstream of the initiation codon ATG for immunoglobulin.
(3) Construction of pEPKMA1, pEPKMB1 and pAGE501
The original immunoglobulin promoter and enhancer are positionally separated. Therefore, it was necessary to construct a vector containing the promoter and enhancer connected to each other for use of said vector as a heterologous protein expression vector. Accordingly, the following procedure was followed.
Thus, 1 .mu.g of the 9.3 kb immunoglobulin H chain variable region gene obtained in Paragraph 1 (5) was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of EcoRV and 10 units of XbaI were added, and the mixture was incubated at 37.degree. C. for 2 hours for causing cleavage at the EcoRV and XbaI sites. The reaction mixture was subjected to agarose gel electrophoresis and 0.1 .mu.g of a DNA fragment (about 1 kb) containing the immunoglobulin enhancer region was recovered. Separately, 1 .mu.g of the plasmid pKMD6 obtained in (2) was dissolved in 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of BglII was added, and the mixture was incubated at 37.degree. C. for 2 hours to effect cleavage at the BglII site. After phenol-chloroform extraction, the DNA was precipitated with ethanol and dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 6 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was allowed to proceed at 16.degree. C. for 90 minutes for rendering the 5' protruding ends formed upon BglII digestion blunt-ended. The reaction was terminated by extraction with phenol, the mixture was extracted with chloroform and then subjected to ethanol precipitation, the DNA obtained was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride, 10 units of HindIII was added, and the mixture was incubated at 37.degree. C. for 2 hours to effect cleavage at the HindIII site. The reaction mixture was subjected to agarose gel electrophoresis and 0.1 .mu.g of a DNA fragment (about 0.8 kb) containing the immunoglobulin promoter region was recovered. Then, 0.2 .mu.g of the plasmid pUC18 �Messing: Methods in enzymology 101, 20 (1983)! was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of HindIII and 10 units of XbaI were added, and the mixture was incubated at 37.degree. C. for 2 hours for causing cleavage at the HindIII and XbaI sites. The reaction mixture was subjected agarose gel electrophoresis and 0.1 .mu.g of a DNA fragment of about 2.7 kb in size was recovered. The thus-obtained pPKMD6-derived 0.8 kb DNA fragment (0.1 .mu.g), immunoglobulin enhancer region-containing DNA fragment (0.02 .mu.g) and pUC18 (0.1 .mu.g) were dissolved in 20 .mu.l of T4 ligase buffer, 175 units of T4 DNA ligase was added, and the mixture was incubated at 4.degree. C. for 1 day. The reaction mixture was used to transform Escherichia coli HB101 to give an Ap-resistant colony. The recombinant plasmid DNA was recovered from this colony to give pEPKMA1 shown in FIG. 31.
Then, 1 .mu.g of the plasmid pEPKMA1 was dissolved in 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of XbaI was added, and the mixture was incubated at 37.degree. C. for 2 hours for causing cleavage at the XbaI site. After phenol-chloroform extraction, the resultant DNA fragment was precipitated with ethanol and dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 6 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was allowed to proceed at 16.degree. C. for 90 minutes for rendering the cohesive ends formed upon XbaI digestion blunt-ended. The reaction was terminated by extraction with phenol and, after chloroform extraction, the DNA fragment was recovered by ethanol precipitation. This DNA fragment and a synthetic DNA linker XhoI (Takara Shuzo) (0.01 .mu.g) were dissolved in 20 .mu.l of T4 ligase buffer, 175 units of T4 DNA ligase was added, and the mixture was incubated at 4.degree. C. for 1 day. The reaction mixture was used to transform Escherichia coli HB101 to give an Ap-resistant colony. The recombinant plasmid DNA was recovered from this colony to give pEPKMB1 shown in FIG. 32.
Then, the SV40 early gene promoter and enhancer regions (hereinafter abbreviated as P.sub.SE) of the heterologous gene expression vector pAGE107 for use in animals �Miyaji et al.: Cytotechnology, 3, 133-140 (1990)! were replaced with the KM50-derived immunoglobulin H chain promoter and enhancer (hereinafter abbreviated as P.sub.IH) of pEPKMB1 in the following manner.
One .mu.g of the plasmid pAGE107 was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 150 mM sodium chloride, 10 units of SalI and 10 units of XhoI were added, and the mixture was incubated at 37.degree. C. for 2 hours to effect cleavage at the SalI and XhoI sites. The reaction mixture was subjected to agarose gel electrophoresis and 0.5 .mu.g of a DNA fragment (about 5.95 kb) containing the G418 resistance gene, among others, was recovered. Then, 1 .mu.g of the plasmid pEPKMB1 was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 150 mM sodium chloride, 10 units of SalI and 10 units of XhoI were added, and the mixture was incubated at 37.degree. C. for 2 hours to effect cleavage at the SalI and XhoI sites. The reaction mixture was subjected to agarose gel electrophoresis and 0.1 .mu.g of a DNA fragment (about 1.7 kb) containing the immunoglobulin promoter and enhancer regions was recovered. The thus-obtained pAGE107-derived 5.95 kb DNA fragment (0.1 .mu.g) and immunoglobulin promoter and enhancer region-containing DNA fragment (0.02 .mu.g) were dissolved in 20 .mu.l of T4 ligase buffer, 175 units of T4 DNA ligase was added, and the mixture was incubated at 4.degree. C. for 1 day. The reaction mixture was used to transform Escherichia coli HB101. An Ap-resistant colony was isolated and the recombinant plasmid DNA was recovered therefrom to give pAGE501 shown in FIG. 33.
(4) Construction of pAGE109
A plasmid, pAGE109, derived from pAGE106 by deletion of one of the two EcoRI sites in pAGE106 was constructed as follows.
Thus, 2 .mu.g of the heterologous gene expression vector pAGE106 for use in animal cells as described in EP-A-0 405 285 was added to 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride; 10 units each of EcoRI and SacI were further added, and digestion was conducted at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1.5 .mu.g of a DNA fragment (4.3 kb) resulting from cleavage of pAGE106 with EcoRI and SacI and containing the SV40 early gene promoter and G418 resistance gene was recovered. Then, this DNA fragment was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I large fragment was added, and the reaction was conducted at 16.degree. C. for 2 hours for rendering the 3' protruding ends formed upon SalI digestion and the 5' protruding ends formed upon EcoRI digestion blunt-ended. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in 20 .mu.l of T4 ligase buffer; 350 units of T4 DNA ligase was further added to the mixed solution, and ligation was carried out at 4.degree. C. for 4 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 to give the plasmid pAGE109 shown in FIG. 34.
(5) Construction of pAGE502
For replacing the SV40 promoter and enhancer of pAGE107 with the immunoglobulin H chain promoter and enhancer, a plasmid named pAGE502 was constructed as follows.
Two .mu.g of pAGE107 described in EP-A-0 405 285 was added to 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride, 10 units of HindIII was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was conducted at 16.degree. C. for 2 hours for rendering the 5' protruding ends formed upon HindIII digestion blunt-ended. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of XhoI was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1.5 .mu.g of a DNA fragment (about 5.95 kb), resulting from cleavage of pAGE107 with XhoI and HindIII and containing the G418 resistance gene and Ap resistance, was recovered.
Two .mu.g of pAGES01 obtained in (3) was added to 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 175 mM sodium chloride, 10 units of SalI was further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was conducted at 16.degree. C. for 2 hours for rendering the 5' protruding ends formed upon SalI digestion blunt-ended. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of XhoI was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.2 .mu.g of a DNA fragment (1.8 kb) resulting from cleavage of pAGE501 with XhoI and SalI and containing the KM50 cell immunoglobulin H chain promoter and enhancer was recovered.
Then, 0.1 .mu.g of the HindIII-XhoI fragment (about 5.95 kb) of pAGE107 as obtained above and 0.1 .mu.g of the SalI-XhoI fragment (about 1.8 kb) of pAGE501 were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 DNA ligase was added to the solution, and the mixture was incubated at 4.degree. C. for 1 day. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 to give the plasmid PAGE502 shown in FIG. 35.
(6) Construction of pAGE503
A plasmid named pAGE503 derived from pAGE502 by deletion of one of the two EcoRI sites was constructed as follows.
Two .mu.g of pAGE109 obtained in (4) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride; 10 units of HindIII and 10 units of ClaI were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.2 .mu.g of a DNA fragment (about 1 kb) resulting from cleavage of pAGE109 with ClaI and HindIII and containing the poly-A signal gene for the beta globulin and SV40 early genes was recovered.
Then, 2 .mu.g of pAGE502 obtained in (5) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride, 10 units of HindIII and 10 units of ClaI were further added, and digestion was conducted at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1 .mu.g of a DNA fragment (about 6.1 kb) resulting from cleavage of pAGE502 with HindIII and ClaI and containing the KM50 cell immunoglobulin H chain promoter and enhancer genes, the Ap resistance gene and the G418 resistance gene was recovered by the DEAE paper method. Then, 0.1 .mu.g of the HindIII-ClaI fragment (about 1 kb) of pAGE109 as obtained above and 0.1 .mu.g of the HindIII-ClaI fragment (about 6.1 kb) of pAGE502 as obtained above were dissolved in a total of 20 .mu.l of T4 ligase buffer, 350 units of T4 DNA ligase was added to the solution, and the mixture was incubated at 4.degree. C. for 1 day. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pAGES03 shown in FIG. 36 was obtained.
(7) Construction of pSE1d1
A plasmid named pSEldl was constructed by introducing the dhfr gene into pAGE107, as follows.
Two .mu.g of pAGE107 described in EP-A-0 405 825 was added to 100 .mu.l of 100 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride, 10 units of EcoRI was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was conducted at 16.degree. C. for 2 hours for rendering the 5' protruding ends formed upon EcoRI digestion blunt-ended. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride; 10 units of HindIII was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1.5 .mu.g of a DNA fragment (about 5.6 kb) resulting from cleavage of pAGE107 with EcoRI and HindIII and containing the G418 resistance gene and Ap resistance gene was recovered.
Two .mu.g of pSV2-dhfr �Subramani et al.: Mol. Cell. Biol., 1, 854 (1981)! was added to 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of BglII was further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was conducted at 16.degree. C. for 2 hours for rendering the 5' protruding ends formed upon BglII digestion blunt-ended. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of HindIII was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.2 .mu.g of a pSV2-dhfr DNA fragment (0.76 kb) resulting from cleavage with BglII and HindIII and containing the dehydrofolate reductase (dhfr) gene was recovered.
Then, 0.1 .mu.g of the HindIII-EcoRI fragment (about 5.6 kb) of pAGE107, as obtained above, and 0.1 .mu.g of the BglII-HindIII fragment (about 0.76 kb) of pSV2-dhfr, as obtained above, were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 DNA ligase was added to the solution, and the mixture was incubated at 4.degree. C. for 1 day. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pSE1d1 shown in FIG. 37 was obtained.
(8) Construction of pSE1d2
A plasmid named pSE1d2 was constructed by deleting the HindIII cleavage site from pSE1d1, as follows.
Thus, 2 .mu.g of pSE1d1 obtained in (7) was added to 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride, 10 units of HindIII was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was conducted at 16.degree. C. for 2 hours for rendering the 5' protruding ends formed upon HindIII digestion blunt-ended. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in 20 .mu.l of T4 ligase buffer, 350 units of T4 DNA ligase was added to the solution, and the mixture was incubated at 4.degree. C. for 1 day. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pSE1d2 shown in FIG. 38 was obtained.
(9) Construction of pIg1SE1d2
A plasmid named pIg1SE1d2 was constructed by introducing the dhfr gene into pAGE503, as follows.
Two .mu.g of pAGE503 obtained in (6) was added to 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride, 10 units of ClaI was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was conducted at 16.degree. C. for 2 hours for rendering the 5' protruding ends formed upon ClaI digestion blunt-ended. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride; 10 units of MluI was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1 .mu.g of a DNA fragment (about 5.4 kb) resulting from cleavage of pAGE503 with ClaI and MluI and containing the KM50 immunoglobulin H chain promoter and enhancer was recovered.
Then, 2 .mu.g of pSE1d2 obtained in (8) was added to 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of XhoI was further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was conducted at 16.degree. C. for 2 hours for rendering the 5' protruding ends formed upon XhoI digestion blunt-ended. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of MluI was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1 .mu.g of a DNA fragment (about 3.8 kb) resulting from cleavage of pSE1d2 with XhoI and MluI and containing the dhfr gene was recovered.
Then, 1 .mu.g of the ClaI-MluI fragment (about 5.4 kb) of pAGE503 as obtained above and 1 .mu.g of the XhoI-MluI fragment (about 3.8 kb) of pSE1d2 as obtained above were dissolved in a total of 20 .mu.l of T4 ligase buffer, 350 units of T4 DNA ligase was added to the solution, and the mixture was incubated at 4.degree. C. for 1 day. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pIg1SE1d2 shown in FIG. 39 was obtained.
(10) Construction of pIg1SE1d3
A plasmid named pIg1SE1d3 was constructed by deleting the ApaI cleavage site from pIg1SE1d2, as follows.
Two .mu.g of pIg1SE1d2 obtained in (9) was added to 100 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride, 10 units of ApaI was further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was carried out at 16.degree. C. for 2 hours for rendering the 3' protruding ends formed upon ApaI digestion blunt-ended. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in 20 .mu.l of T4 ligase buffer, 350 units of T4 ligase was added to the solution, and ligation was effected at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pIg1SE1d3 shown in FIG. 40 was obtained.
(11) Construction of pIg1SE1d4
For providing pIg1SE1d3 with a cloning site between the HindIII cleavage site and EcoRI cleavage site, a plasmid named pIg1SE1d4 was constructed containing the synthetic DNA defined by SEQ ID NO:17 as an insert, as follows.
Two .mu.g of pIg1SE1d3 obtained in (10) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride, 10 units each of HindIII and EcoRI were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1 .mu.g of a DNA fragment (about 9.2 kb) resulting from cleavage of pIg1SE1d3 with HindIII and EcoRI and containing the KM50 cell immunoglobulin H chain promoter, enhancer, Ap resistance gene, G418 resistance gene and dhfr gene was recovered.
Then, 0.1 .mu.g of the HindIII-EcoRI fragment (about 9.2 kb) of pIg1SE1d3 as obtained above and 10 ng of the synthetic DNA (SEQ ID NO:17) were a total of 20 .mu.l of T4 ligase buffer, 350 units of T4 DNA ligase was added to the solution, and the mixture was incubated at 4.degree. C. for 1 day. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pIg1SE1d4 shown in FIG. 41 was obtained.
3. Preparation of the Moloney Mouse Leukemia Virus Long Terminal Repeat (hereinafter abbreviated as "MoLTR")
It is known that MoLTR has promoter and enhancer activity �Kuwana et al.: Biochem. Biophys. Res. Commun., 149, 960 (1987)!. Therefore, for using MoLTR as a promoter and enhancer in vectors for chimeric human antibody expression, a plasmid, pPMOL3, containing MoLTR was constructed as follows.
Three .mu.g of pPMOL1 described in JP-A-1-63394 was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 7 mM magnesium chloride and 6 mM 2-mercaptoethanol, 10 units of ClaI was further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment was added, and the reaction was carried out at 16.degree. C. for 2 hours for rendering the 5' protruding ends formed upon ClaI digestion blunt-ended. The reaction was terminated by extraction with phenol, the reaction mixture was subjected to chloroform extraction and then to ethanol precipitation, and 2 .mu.g of a DNA fragment was recovered. This DNA fragment and 0.01 .mu.g of a synthetic DNA linker XhoI (Takara Shuzo) were dissolved in 20 .mu.l of T4 ligase buffer, 175 units of T4 DNA ligase was added, and the mixture was incubated at 4.degree. C. for 1 day. The reaction mixture was used to transform Escherichia coli HB101 and the plasmid pPMOL2 shown in FIG. 42 was obtained. Then, 3 .mu.g of pPMOL2 was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 7 mM magnesium chloride, 10 mM sodium chloride and 6 mM 2-mercaptoethanol, 10 units of SmaI was further added, and digestion was conducted at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, and 2 .mu.g of a DNA fragment was recovered. This DNA fragment and 0.01 .mu.g of a synthetic DNA linker (EcoRI; Takara Shuzo) were dissolved in 20 .mu.l of T4 ligase buffer, 175 units of T4 DNA ligase was added, and the mixture was incubated at 4.degree. C. for 1 day. The reaction mixture was used to transform Escherichia coli HB101 and the plasmid pPMOL3 shown in FIG. 43 was obtained.
4. Cloning of the Human Immunoglobulin IgGl H Chain Constant Region (C.gamma.1) cDNA and L Chain Constant Region (C.kappa.) cDNA
(1) Isolation of mRNA from the chimeric antibody producer cell line SP2-PC Chimera-1
Using mRNA extraction kit Fast Track (product number K1593-02) manufactured by Invitrogen, MRNA (6.2 .mu.g) was isolated from 1.times.10.sup.8 cells of the chimeric antibody producer cell line SP2-PC Chimera-1 described in FEBS Letters, 244, 301-306 (1989) and capable of producing a chimeric antibody having anti-phosphorylcholine activity.
(2) Construction of an SP2-PC Chimera-1 cDNA library and cloning of the human immunoglobulin H chain constant region (C.gamma.1) cDNA and L chain constant region (C.kappa.) cDNA
Starting with 2 .mu.g of the MRNA obtained in (1) and using cDNA Synthesis Kit (product number 27-9260-01) manufactured by Pharmacia, EcoRI adapter joining was performed, followed by phosphorylation. The cDNA solution obtained was subjected to phenol-chloroform extraction and then to ethanol precipitation, and 4 .mu.g of cDNA was recovered. This cDNA was dissolved in 20 .mu.l of sterilized water and then fractionated by agarose gel electrophoresis, and about 0.3 .mu.g each of two DNA fragments, about 1.8 kb and about 1.0 kb in size, were recovered.
Then, 5 .mu.g of the vector pUC18 was added to 100 .mu.l of 100 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 50 units of EcoRI was further added, and digestion was carried out at 37.degree. C. for 4 hours for cleaving the pUC18 DNA at the EcoRI site. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, and about 3 .mu.g of a DNA fragment resulting from cleavage of pUC18 at the EcoRI site thereof was recovered.
Then, 0.1 .mu.g of the EcoRI fragment (about 2.7 kb) of pUC18 as obtained above and 0.1 .mu.g each of the 1.8 kb and 1.0 kb cDNA fragments prepared from SP2-PC Chimera-1 cells were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 DNA ligase was added to the solution, and ligation was effected at 4.degree. C. for 24 hours.
The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli LE392. About 3,000 colonies obtained were fixed onto a nitrocellulose filter. From among the strains firmly bound at 65.degree. C. to probes prepared by labeling the human immunoglobulin constant region chromosomal genes (IgG1 H chain constant region C.gamma.1 and L chain constant region C.gamma.) �Kameyama et al.: FEBS Letters, 244, 301 (1989)! with .sup.32 P, a plasmid (pPCVHhCGI1) associable with C.gamma.1 and another (pPCVLhCK1) associable with C.kappa. were isolated.
(3) Introduction of an EcoRV site into the human Ig.kappa. chain constant region gene
An EcoRV site was introduced into the human Ig.kappa. chain constant region at a site near the 5' end thereof by site-directed mutagenesis using a kit (catalog number Q6210) manufactured by Promega. The plasmid pPCVLhCK1 (2 .mu.g) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride, 10 units of EcoRI and 10 units of KpnI were further added, and digestion was conducted at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.2 .mu.g of a DNA fragment (about 0.8 kb) resulting from cleavage of pPCVLhCK1 with KpnI and EcoRI and containing the human immunoglobulin L chain constant region gene was recovered.
Then, 2 .mu.g of pSELECT1 (a kit manufactured by Promega; catalog number Q6210) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 50 mM sodium chloride, 10 units each of EcoRI and KpnI were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1 .mu.g of a DNA fragment (about 5.7 kb) resulting from cleavage of pSELECT1 with EcoRI and KpnI was recovered.
Then, 0.1 .mu.g of the EcoRI-KpnI fragment (about 0.8 kb) of pPCVLhCK1 as obtained above and 0.1 .mu.g of the EcoRI-KpnI fragment (about 5.7 kb) of pSELECT1 as obtained above were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 DNA ligase was added to the solution, and ligation was effected at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli JM109 and the plasmid pchCKA7 shown in FIG. 44 was obtained.
Then, using pchCKA7 and using the synthetic DNA defined by SEQ ID NO:18 as a mutagenic primer, the sequence covering the 12th base to 14 base from the N terminus of the human immunoglobulin L chain constant region, namely ACC, was converted to GAT and thus an EcoRV site was introduced into that site, to give a plasmid named pchCKB1 (FIG. 45).
Then, the EcoRV site of pchCKB1 was converted to a HindIII cleavage site in the following manner.
Thus, 2 .mu.g of the plasmid pchCKB1 was added to 10 .mu.l of 100 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of EcoRI was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the precipitate was dissolved in a total of 40 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived polymerase I Klenow fragment was added, and the reaction was carried out at 37.degree. C. for 30 minutes for rendering the 5' protruding ends formed upon EcoRI digestion blunt-ended. The reaction mixture was subjected to phenol-chloroform extraction and then ethanol precipitation, the precipitate was dissolved, together with 0.1 .mu.g of a HindIII linker (Takara Shuzo), in 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was added to the solution, and ligation was effected at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pchCKC1 shown in FIG. 46 was obtained.
5. Construction of Vectors for Chimeric Human Antibody H Chain Expression
(1) Construction of a vector to be used in constructing chimeric human antibody H chain expression vectors (vector for chimeric human antibody H chain expression)
The plasmid pIg1SE1d4 obtained in Paragraph 2 (11) (2 .mu.g) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units each of EcoRV and ApaI were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1.5 .mu.g of a DNA fragment (about 9.2 kb) resulting from cleavage of pIg1SE1d4 with EcoRV and ApaI was recovered.
Then, 2 .mu.g of pPCVHhCGI1 obtained in Paragraph 4 (2) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride, 10 units of ApaI and 10 units of SmaI were further added, and digestion was conducted at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.2 .mu.g of a DNA fragment (about 1 kb) resulting from cleavage of pPCVHhCGI1 with ApaI and SmaI and containing the human immunoglobulin H chain constant region gene was recovered.
Then, 0.1 .mu.g of the EcoRV-ApaI fragment (about 9.2 kb) of pIg1SE1d4 as obtained above and 0.1 .mu.g of the ApaI-SmaI fragment (about 1 kb) of pPCVHhCGI1 as obtained above were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 DNA ligase was added to the solution, and ligation was conducted at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the vector pCHiIgHB2 for chimeric human antibody H chain expression as shown in FIG. 47 was obtained.
(2) Construction of a vector to be used in constructing chimeric human antibody L chain expression vectors (vector for chimeric human antibody L chain expression)
The plasmid pIg1SE1d4 obtained in Paragraph 2 (11) (2 .mu.g) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of EcoRV and 10 units of HindIII were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 1.5 .mu.g of a DNA fragment (about 9.2 kb) resulting from cleavage of pIg1SE1d4 with EcoRV and HindIII was recovered.
Then, 2 .mu.g of pckCKC1 obtained in Paragraph 4 (3) was added to 30 .mu.l of 10 mM Tris-hydrochloride (pH 7.5) containing 6 mM magnesium chloride and 100 mM sodium chloride, 10 units of EcoRV and 10 units of HindIII were further added, and digestion was carried out at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.2 .mu.g of a DNA fragment (about 0.6 kb) resulting from cleavage of pPCVLhCK1 with EcoRV and HindIII and containing the human immunoglobulin L chain constant region gene was recovered.
Then, 0.1 .mu.g of the EcoRV-HindIII fragment (about 9.2 kb) of pIg1SE1d4 as obtained above and 0.1 .mu.g of the EcoRV-HindIII fragment (about 0.6 kb) of pchCKC1 as obtained above were dissolved in a total of 20 .mu.l of T4 ligase buffer, 350 units of T4 DNA ligase was added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the vector pChiIgLA1 for chimeric human antibody L chain expression as shown in FIG. 48 was obtained.
REFERENCE EXAMPLE 2
Construction of a Chimeric Human Antibody H Chain Expression Vector, pChi641HA1
1. Isolation of MRNA from mouse anti-GD.sub.3 monoclonal antibody KM-641-producing hybridoma cells
Using mRNA extraction kit Fast Track (product number K1593-02) manufactured by Invitrogen, 34 .mu.g of mRNA was isolated from 1.times.10.sup.8 mouse anti-GD.sub.3 monoclonal antibody KM-641-producing hybridoma cells obtainable as in Reference Example 1.
2. Construction of a KM-641 H chain cDNA library and a KM-641 L chain cDNA library
Using 3 .mu.g of the mRNA obtained in Paragraph 1 and using cDNA synthesis kit ZAP-cDNA Synthesis Kit (product number sc200400) manufactured by Stratagene, cDNA having an EcoRI adapter at the 5' terminus and cDNA having an XhoI adapter at the 3' terminus were synthesized. About 6 .mu.g of each cDNA was dissolved in 10 .mu.l of sterilized water and fractionated by agarose gel electrophoresis. In this way, about 0.1 .mu.g of a cDNA fragment having a size of about 1.8 kb and corresponding to the H chain and a cDNA fragment having a size of about 1.0 kb and corresponding to the L chain were recovered. Then, 0.1 .mu.g of the cDNA fragment of about 1.8 kb in size, 0.1 .mu.g of the cDNA fragment of about 1.0 kb in size and 1 .mu.g of Uni-ZAP XR (Stratagene; derived from the Lambda ZAPII vector by cleavage with EcoRI and XhoI, followed by treatment with calf intestine alkaline phosphatase), to be used as the vector, were dissolved in T4 ligase buffer; 175 units of T4 DNA ligase was added, and the mixture was incubated at 12.degree. C. for 10 hours and further at room temperature for 2 hours. A 4-.mu.l portion of the reaction mixture was packaged into the lambda phage by the conventional method �Maniatis et al. (ed.): Molecular Cloning, 1989, p. 2.95! using Giga Pak Gold (Stratagene), followed by transfection of Escherichia coli PLK-F with the packaging mixture by the conventional method �Maniatis et al. (ed.): Molecular Cloning, 1989, p. 2.95-107!. As an H chain cDNA library and as an L chain cDNA library, about 10,000 phage clones were respectively obtained. The phages were then fixed onto nitrocellulose filters by the conventional method �Maniatis et al. (ed.): Molecular Cloning, 1989, p. 2.112!.
3. Cloning of the monoclonal antibody KM-641 H chain and L chain cDNAs
Using probes prepared by labeling a mouse C.gamma.1 gene (mouse immunoglobulin constant region chromosomal gene)-containing EcoRI fragment (about 6.8 kb) �Roeder et al.: Proc. Natl. Acad. Sci. U.S.A., 78, 474 (1981)! and a mouse C.kappa. gene-containing HindIII-BamHI fragment (about 3 kb) �Sakano et al.: Nature, 280, 288 (1979)! with .sup.32 P, one phage clone strongly associable with the former probe at 65.degree. C. and one phage clone strongly associable with the latter probe at 65.degree. C. were isolated from the H chain cDNA library and L chain cDNA library constructed in Paragraph 2 in accordance with the conventional method �Maniatis et al. (ed.): Molecular Cloning, 1989, p. 2.108!. Then, by converting the phage clones to pBluescript plasmids using cDNA synthesis kit ZAP-cDNA Synthesis Kit (product number sc200400) manufactured by Stratagene, a KM-641 H chain cDNA-containing recombinant plasmid, pKM641HA3, and a KM-641 L chain cDNA-containing recombinant plasmid, pKM641LA2, were obtained. Cleavage of pKM641HA3 and pKM641LA2 with EcoRI and XhoI revealed that a cDNA fragment of about 1.6 kb and a cDNA fragment of about 0.9 kb had been inserted therein, respectively (FIG. 49).
4. Base sequences of the immunoglobulin variable regions in the KM-641 H chain cDNA (pKM641HA3) and KM-641 L chain cDNA (pKM641LA2)
The base sequences of the immunoglobulin regions in pKM641HA3 and pKM641LA2 obtained in Paragraph 3 were determined by the dideoxy method �Maniatis et al. (ed.): Molecular Cloning, 1989, p. 13.42! using Sequenase Version 2.0 DNA Sequencing Kit (United States Biochemical Corporation). The results obtained are shown in SEQ ID NO:19 and SEQ ID NO:20. In pKM641LA2, a methionine codon, presumably the initiation codon ATG, was found in the vicinity of the 5' terminus and the cDNA was a leader sequence-containing full-length one. In pKM641HA3, no methionine initiation codon was found and the leader sequence was partly lacking.
5. Construction of a KM-641-derived chimeric human antibody H chain expression vector
A chimeric human antibody H chain expression vector was constructed by joining the H chain variable region gene obtained by cleaving the plasmid pKM641HA3 at the AluI site near the 5' terminus of the variable region gene and at the StyI site near the 3' terminus of the variable region gene to the vector for chimeric human antibody H chain expression as obtained in Reference Example 1 using the synthetic DNAs defined by SEQ ID NO:21 and SEQ ID NO:22 (FIG. 50).
First, the DNA defined by SEQ ID NO:22 composed of the base sequence from the 3' terminus of the immunoglobulin H chain variable region in pKM641HA3 to the StyI cleavage site near said 3'terminus and the base sequence from the 5' terminus of the immunoglobulin H chain constant region in pAGE28 to the ApaI cleavage site near said 5' terminus and having a StyI cleavage site and an ApaI cleavage site on the respective termini (cf. FIG. 50) was synthesized using a DNA synthesizer. This synthetic DNA was then introduced into the plasmid pKM641HA3 in the following manner.
Three .mu.g of pKM641HA3 was added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of StyI were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a 0.41 kb DNA fragment was recovered. Then, 3 .mu.g of pAGE28 �Mizukami et al.: J. Biochem., 101, 1307-1310 (1987)! was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 7 mM magnesium chloride and 6 mM 2-mercaptoethanol, 10 units of EcoRI and 10 units of ApaI were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 2 .mu.g of a 2.45 kb DNA fragment was recovered. Then, 0.1 .mu.g of the EcoRI-StyI fragment (about 0.41 kb) of pKM641HA3, as obtained above, 0.1 .mu.g of the EcoRI-ApaI fragment (about 2.45 kb) of pAGE28, as obtained above, and 0.3 .mu.g of the synthetic DNA, defined by SEQ ID NO:22, were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was added to the solution, and ligation was conducted at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pKM641HE1 shown in FIG. 51 was obtained.
Since pKM641HE1 had no leader sequence, the following measure was taken to supplement the deficit using the synthetic DNA defined by SEQ ID NO:21.
pKM641HE1 (3 .mu.g) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 7 mM magnesium chloride and 6 mM 2-mercaptoethanol, 10 units of EcoRI and 10 units of ApaI were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.4 .mu.g of a DNA fragment of about 0.42 kb in size was recovered. The EcoRI-ApaI fragment (about 0.42 kb; 0.4 .mu.g) of pKM641HE1 was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 7 mM magnesium chloride, 50 mM sodium chloride and 6 mM 2-mercaptoethanol, 10 units of AluI was further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, and about 0.3 .mu.g of a DNA fragment of about 0.4 kb in size was recovered.
Then, 0.1 .mu.g of the AluI-ApaI fragment (about 0.4 kb) of pKM641HE1 as obtained above, 0.1 .mu.g of the EcoRI-ApaI fragment (about 2.45 kb) of pAGE28 as obtained above and 0.3 .mu.g of the synthetic DNA defined by SEQ ID NO:21 were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pKM641HF1 shown in FIG. 52 was obtained.
Then, the immunoglobulin H chain variable region of pKM641HF1 was introduced into the vector pChiIgHB2 for chimeric human antibody H chain expression, as follows. pKM641HF1 (3 .mu.g) was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 7 mM magnesium chloride and 6 mM 2-mercaptoethanol, 10 units of EcoRI and 10 units of ApaI were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.5 .mu.g of a 0.44 kb DNA fragment was recovered. Then, 3 .mu.g of pChiIgHB2 was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 7 mM magnesium chloride and 6 mM 2-mercaptoethanol, 10 units of EcoRI and 10 units of ApaI were further added, and digestion was conducted at 37.degree. C. for 4 hours. The reaction mixture was subjected to phenol-chloroform extraction and about 3 .mu.g of DNA was recovered. Then, 0.1 .mu.g of the EcoRI-ApaI fragment (about 0.44 kb) of pKM641HF1 as obtained above and 0.1 .mu.g of the EcoRI-ApaI fragment (about 10.1 kb) of pChiIgHB2 as obtained above were dissolved in a total of 20 .mu.l of T4 ligase buffer; 350 units of T4 ligase was added to the solution, and ligation was carried out at 4.degree. C. for 24 hours. The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid pChi641HA1 shown in FIG. 53 was obtained.
Then, the KM50-derived immunoglobulin H chain promoter and enhancer region of pChi641HA1 was replaced with MoLTR, as follows.
pChi641HA1 (3 .mu.g) was added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of XhoI were further added, and digestion was effected at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.2 .mu.g of a DNA fragment of about 8.8 kb in size was recovered. pPMOL3 (3 .mu.g) obtained in Example 1, Paragraph 2 was added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT; 10 units of EcoRI and 10 units of XhoI were further added, and digestion was carried out at 37.degree. C. for 4 hours. The reaction mixture was fractionated by agarose gel electrophoresis and about 0.3 .mu.g of a MoLTR-containing DNA fragment (0.63 kg) was recovered. Then, 0.1 .mu.g of the EcoRI-XhoI fragment of pChi641HA1 and 0.1 .mu.g of the EcoRI-XhoI fragment of pPMOL3 were dissolved in 20 .mu.l of T4 ligase buffer, 175 units of T4 DNA ligase was added, and the mixture was incubated at 4.degree. C. for 1 day. The reaction mixture was used to transform Escherichia coli HB101 and the KM-641-derived chimeric human H chain expression vector pChi641HAM1 shown in FIG. 54 was obtained.
EXAMPLE 2
Production of human CDR-transplanted anti-GM.sub.2 antibodies (1)
1. Construction of DNAs Each Coding For Human CDR-Transplanted Anti-GM.sub.2 Antibody H Chain Variable Region and Human CDR-transplanted Anti-GM.sub.2 Antibody L Chain Variable Region
(1) Construction of DNA coding for human CDR-transplanted anti-GM.sub.2 antibody H chain variable region
A DNA coding for a human CDR-transplanted anti-GM.sub.2 antibody H chain variable region, hKM796H, which contains amino acid sequences of SEQ ID NO:94, SEQ ID NO:95 and SEQ ID NO:96, was constructed in the following manner.
NEWM �BIO/TECHNOLOGY, 9, 266 (1991)! was used as human antibody H chain variable region-encoding DNA to which each CDR was to be transplanted. DNAs set forth in SEQ ID NO:23 through NO:29 corresponding to NEWM in which each CDR was replaced with amino acid sequences of SEQ ID NO:94, SEQ ID NO:95 and SEQ ID NO:96 were synthesized using an automatic DNA synthesizer (model 380A manufactured by Applied Biosystems Co., Ltd.). The thus-obtained synthetic DNAs (50 picomoles each) were dissoloved in 20 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.6) containing 10 mM magnesium chloride, 5 mM DTT, 0.1 mM EDTA and 0.5 mM ATP, 5 units of T4 polynucleotide kinase was added, and 5'-phosphorylation was carried out at 37.degree. C. for 30 minutes. Ten picomoles each of the resulting phosphorylated synthetic DNAs, which had restriction enzyme sites on both ends, were ligated in the order of SEQ ID NO. (SEQ ID NO:23 throuth NO:29) using a DNA ligation kit (Takara Shuzo) in accordance with the manufacturer's instruction attached to the kit to obtain a DNA, hKM796H, shown in FIG. 55. The amino acid sequence corresponding to hKM796H is shown in SEQ ID NO:100.
(2) Construction of DNA coding for human CDR-transplanted anti-GM.sub.2 antibody L chain variable region
A DNA coding for a human CDR-transplanted anti-GM.sub.2 antibody L chain variable region, hKM796L, which contains amino acid sequences of SEQ ID NO:97, SEQ ID NO:98 and SEQ ID NO:99, was constructed in the following manner.
REI �BIO/TECHNOLOGY, 9, 266 (1991)! was used as human antibody L chain variable region-encoding DNA to which each CDR was to be transplanted. DNAs set forth in SEQ ID NO:30 through NO:35 corrresponding to REI in which each CDR was replaced with amino acid sequences of SEQ ID NO:97, SEQ ID NO:98 and SEQ ID NO:99 were synthesized using an automatic DNA synthesizer (model 380A manufactured by Applied Biosystems Co., Ltd.). The thus-obtained synthetic DNAs (50 picomoles each) were dissoloved in 20 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.6) containing 10 mM magnesium chloride, 5 mM DTT, 0.1 mM EDTA and 0.5 mM ATP, 5 units of T4 polynucleotide kinase was added, and 5'-phosphorylation was carried out at 37.degree. C. for 30 minutes. Ten picomoles each of the resulting phosphorylated synthetic DNAs, which had restriction enzyme sites on both ends, were ligated in the order of SEQ ID NO. (SEQ ID NO:30 through NO:35) using a DNA ligation kit (Takara Shuzo) in accordance with the manufacturer's instruction attached to the kit to obtain a DNA, hKM796L, shown in FIG. 56. The amino acid sequence corresponding to hKM796L is shown in SEQ ID NO:101.
2. Construction of Human CDR-Transplanted Antibody H Chain Expression Vector and Human CDR-Transplanted Antibody L Chain Expression Vector
(1) Construction of human CDR-transplanted antibody H chain expression vector
A NotI-ApaI fragment of the DNA coding for human CDR-transplanted antibody H chain variable region, obtained in Paragraph 1(1) of Example 2, was ligated to the plasmid pChi796HM1, obtained in Paragraph 7(3) of Example 1, in the following manner (FIG. 57).
Three .mu.g of pChi796HM1, obtained in Paragraph 7(3) of Example 1, were dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of ApaI were added thereto and the mixture was allowed to react at 37.degree. C. for 1 hour. The resulting mixture was subjected to ethanol precipitation and the thus-obtained precipitate was dissolved in 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT. Ten units of NotI were added thereto to allow the mixture to react at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 2 .mu.g of a DNA fragment of about 9.0 kb. Then, about 0.1 .mu.g of the thus-obtained ApaI-NotI fragment of pChi796HM1 was ligated to 0.5 pmoles of the NotI-ApaI fragment of the DNA coding for human CDR-transplanted antibody H chain variable region, obtained in Paragraph 1(1) of Example 2, using a DNA ligation kit (Takara Shuzo). The resulting recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid phKM796HM1 shown in FIG. 57 was obtained.
Then, a human CDR-transplanted antibody H chain expression vector was constructed by introducing .beta.-globin 3' splicing signal into the plasmid phKM796HM1 in the following manner (FIG. 58).
Three .mu.g of phKM796HM1 were added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 1 unit of KpnI was added thereto. The mixture was allowed to react at 37.degree. C. for 10 minutes to effect partial digestion. The resulting mixture was subjected to ethanol precipitation and the thus-obtained precipitate was dissolved in 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT. After adding 1 unit of XhoI, the mixture was allowed to react at 37.degree. C. for 10 minutes to effect partial digestion. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 0.2 .mu.g of a DNA fragment of about 2.1 kb. Separately, 3 .mu.g of pAGE148, obtained in Paragraph 7(2) of Example 1, were added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT. Ten units of KpnI were added thereto to allow the mixture to react at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation and the thus-obtained precipitate was dissloved in 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT. After adding 10 units of XhoI, the mixture was allowed to react at 37.degree. C. for 1 hour and then fractionated by agarose gel electrophoresis to recover about 1 .mu.g of a DNA fragment of about 8.7 kb. One tenth .mu.g of the thus-obtained XhoI-KpnI fragment of phKM796HM1 was ligated to 0.1 .mu.g of the XhoI-KpnI fragment of pAGE148 using a DNA ligation kit (Takara Shuzo). The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 to obtain the plasmid phKM796HMS1 shown in FIG. 58.
(2) Construction of human CDR-transplanted antibody L chain expression vector
An EcoRI fragment having blunt ends of the DNA coding for human CDR-transplanted antibody L chain variable region, obtained in Paragraph 1 (2) of Example 2, was ligated to the chimeric human antibody L chain expression vector pChiIgLA1 in the following manner (FIG. 59).
Three .mu.g of pChiIgLA1, obtained in Reference Example 1, were added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of EcoRV were added thereto and the mixture was allowed to react at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 1 .mu.g of a DNA fragment of about 8.6 kb. Then, about 0.1 .mu.g of the thus-obtained EcoRI-EcoRV fragment of pChiIgLA1 was ligated to 0.5 pmoles of the EcoRI fragment having blunt ends derived from the DNA coding for human CDR-transplanted antibody L chain variable region, obtained in Paragraph 1(2) of Example 2, using a DNA ligation kit (Takara Shuzo). The resulting recombinant plasmid DNA was used to transform Escherichia coli HB101 and the plasmid phKM796LI1 shown in FIG. 59 was obtained.
Then, P.sub.MO was introduced into the plasmid phKM796LI1 in the following manner (FIG. 60).
Three .mu.g of phKM796LI1 were added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of EcoRI and 10 units of XhoI were added thereto, and the mixture was allowed to react at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 1 .mu.g of a DNA fragment of about 8.2 kb. Separately, 3 .mu.g of the chimeric human antibody H chain expression vector pChi641HAM1, obtained in Reference Example 2, were added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT. Ten units of EcoRI and 10 units of XhoI were added thereto to allow the mixture to react at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 0.3 .mu.g of a DNA fragment of about 0.6 kb. One tenth .mu.g of the thus-obtained EcoRI-XhoI fragment of pChi641HAM1 was ligated to 0.1 .mu.g of the EcoRI-XhoI fragment of phKM796LI1 using a DNA ligation kit (Takara Shuzo). The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 to obtain the plasmid phKM796LM1 shown in FIG. 60.
Then, a human CDR-transplanted antibody L chain expression vector was constructed by introducing .beta.-globin 3' splicing signal into the plasmid phKM796LM1 in the following manner (FIG. 61).
Three .mu.g of phKM796LM1 were added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of KpnI were added thereto, and the mixture was allowed to react at 37.degree. C. for 1 hour. The resulting mixture was subjected to ethanol precipitation and the thus-obtained precipitate was dissolved in 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT. After adding 10 units of XhoI, the mixture was allowed to react at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 0.3 .mu.g of a DNA fragment of about 1.6 kb. Separately, 3 .mu.g of pAGE148, obtained in Paragraph 7(2) of Example 1, were added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mm magnesium chloride and 1 mM DTT. Ten units of KpnI were added thereto to allow the mixture to react at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation and the thus-obtained precipitate was dissloved in 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT. After adding 10 units of XhoI, the mixture was allowed to react at 37.degree. C. for 1 hour and then fractionated by agarose gel electrophoresis to recover about 1 .mu.g of a DNA fragment of about 8.7 kb. One tenth .mu.g of the thus-obtained XhoI-KpnI fragment of phKM796LM1 was ligated to 0.1 .mu.g of the XhoI-KpnI fragment of pAGE148 using a DNA ligation kit (Takara Shuzo). The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 to obtain the plasmid phKM796LMS1 shown in FIG. 61.
3. Construction of Human CDR-Transplanted Antibody H Chain and L Chain Tandem Expression Vector
A tandem expression vector containing both of cDNA coding for human CDR-transplanted antibody H chain and cDNA coding for human CDR-transplanted antibody L chain was constructed in the following manner (FIG. 62 and FIG. 63). Three .mu.g of phKM796HMS1, obtained in Paragraph 2(1) of Example 2, were dissolved in 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 1 unit of SalI was added thereto and the mixture was allowed to react at 37.degree. C. for 10 minutes to effect partial digestion. The resulting mixture was subjected to ethanol precipitation and the thus-obtained precipitate was dissolved in 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT. Ten units of MluI was added thereto to allow the mixture to react at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 0.2 .mu.g of a DNA fragment of about 5.9 kb. Then, about 2 .mu.g of pAGE107 as described in EP-A-0 405 285 was added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of MluI and 10 units of SalI were added thereto, and the mixture was allowed to react at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 0.2 .mu.g of a DNA fragment of about 3.35 kb. Then, 0.1 .mu.g of the thus-obtained MluI-SalI fragment of phKM796HMS1 was ligated to 0.1 .mu.g of the MluI-SalI fragment of pAGE107 using a DNA ligation kit (Takara Shuzo). The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 to obtain the plasmid phKM796H107 shown in FIG. 62.
Then, 3 .mu.g of phKM796H107 were added to 30 .mu.l of 10 mM Tris-hydrochloride (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of ClaI was added thereto and the mixture was allowed to react at 37.degree. C. for 1 hour. The reaction mixture was subjected to phenol-chloroform extraction and ethanol precipitation. The resulting precipitate was dissolved in 20 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment were added, and the 5' cohesive ends produced by ClaI digestion were rendered blunt by incubation at 22.degree. C. for 30 minutes. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 0.2 .mu.g of a DNA fragment of about 3.35 kb. The reaction mixture was also subjected to phenol-chloroform extraction and then to ethanol precipitation. The resulting precipitate was dissolved in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of MluI were added thereto and the mixture was allowed to react at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 0.3 .mu.g of a DNA fragment of about 7.5 kb. Separately, 3 .mu.g of phKM796LMS1 were added to 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of XhoI were added and the mixture was allowed to react at 37.degree. C. for 1 hour. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation. The resulting precipitate was dissloved in 20 .mu.l of DNA polymerase I buffer, 5 units of Escherichia coli-derived DNA polymerase I Klenow fragment were added, and the 5' cohesive ends produced by XhoI digestion were rendered blunt by incubation at 22.degree. C. for 30 minutes. The reaction mixture was subjected to phenol-chloroform extraction followed by ethanol precipitation. The resulting precipitate was added to 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT, 10 units of MluI were added thereto, and the mixture was allowed to react at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis to recover about 0.3 .mu.g of a DNA fragment of about 9.3 kb. Then, 0.1 .mu.g of the thus-obtained MluI-ClaI fragment of phKM796H107 was ligated to 0.1 .mu.g of the MluI-XhoI fragment of phKM796LMS1 using a DNA ligation kit (Takara Shuzo). The thus-obtained recombinant plasmid DNA was used to transform Escherichia coli HB101 to obtain the plasmid phKM796HL1 shown in FIG. 63.
4. Expression of Human CDR-Transplanted Anti-GM.sub.2 Antibody in YB2/0 Cells
The plasmids were introduced into YB2/0 cells by the electroporation method of Miyaji et al. �Cytotechnology, 3, 133 (1990)!.
After introduction of 4 .mu.g of phKM796HL1 obtained in Paragraph 3 of Example 2 into 4.times.10.sup.6 YB2/0 (ATCC CRL1581) cells, the cells were suspended in 40 ml of RPMI1640-FCS(10) �RPMI1640 medium (Nissui Pharmaceutical) containing 10% of FCS, 1/4 volume of 7.5% NaHCO.sub.3, 3% of 200 mM L-glutamine solution (Gibco) and 0.5% of penicillin-streptomycin solution (Gibco; containing 5,000 units/ml penicillin and 5,000 .mu.g/ml streptomycin)!, and the suspension was distributed in 200-.mu.l portions into wells of 96-well microtiter plates. After 24 hours of incubation at 37.degree. C. in a CO.sub.2 incubator, G418 (Gibco) was added to a concentration of 0.5 mg/ml and then incubation was continued for 1 to 2 weeks. Transformant colonies appeared, the culture fluid was recovered from each well in which the cells had grown to confluence and an enzyme-linked immunosorbent assay (ELISA) described in Paragraph 11 of Example 1 was conducted for anti-GM.sub.2 human CDR-transplanted antibody activity measurement.
The clone showing the highest activity in ELISA among the clones obtained gave a human CDR-transplanted anti-GM.sub.2 antibody content of about 0.1 .mu.g/ml of culture fluid.
Cells of the clone showing the above-mentioned human CDR-transplanted anti-GM.sub.2 antibody activity were suspended in RPMI1640-FCS(10) medium containing 0.5 mg/ml G418 and 50 nM MTX to a concentration of 1 to 2.times.10.sup.5 cells/ml, and the suspension was distributed in 2-ml portions into wells of 24-well plates. Incubation was performed at 37.degree. C. in a CO.sub.2 incubator for 1 to 2 weeks to induce 50 nM MTX-resistant clones. At the time of confluence, the human CDR-transplanted anti-GM.sub.2 antibody activity in each culture fluid was determined by ELISA. The 50 nM MTX-resistant clone showing the highest activity among the clones obtained showed a human CDR-transplanted anti-GM.sub.2 antibody content of about 1.0 .mu.g/ml.
Cells of the above 50 nM MTX-resistant clone were suspended in RPMI1640-FCS(10) medium containing 0.5 mg/ml G418 and 200 nM MTX to a concentration of 1 to 2.times.10.sup.5 cells/ml, and the suspension was distributed in 2-ml portions into wells of 24-well plates. Incubation was carried out at 37.degree. C. in a CO.sub.2 incubator for 1 to 2 weeks to induce 200 nM MTX-resistant clones. At the time of confluence, each culture fluid was assayed for human CDR-transplanted anti-GM.sub.2 antibody activity by ELISA. The 200 nM MTX-resistant clone showing the highest activity among the clones obtained had a human CDR-transplanted anti-GM.sub.2 antibody content of about 5.0 .mu.g/ml.
As described in detail hereinabove, the present invention provides humanized antibodies reacting with the ganglioside GM.sub.2 .
EXAMPLE 3
Production of Human CDR-Transplanted Anti-GM.sub.2 Antibodies (2)
1. Construction of Tandem Cassette Type Humanized Antibody Expression Vector, pKANTEX93
A tandem cassette type humanized antibody expression vector, pKANTEX93, for the expression of a human CDR-transplanted antibody in mammalian cells was constructed based on the plasmid pSE1UK1SEd1-3 described in JP-A-2-257891 by inserting a DNA fragment coding for a human CDR-transplanted anti-GM.sub.2 antibody H chain variable region and a DNA fragment coding for a human CDR-transplanted anti-GM.sub.2 antibody L chain variable region into said plasmid upstream of the human antibody .gamma. 1H chain constant region cDNA and human antibody .kappa. L chain constant region cDNA, respectively, in the following manner.
(1) Modification of ApaI and EcoRI restriction enzyme sites occurring in rabbit .beta.-globin gene splicing and poly A signals
For making it possible to construct a human CDR-transplanted antibody expression vector by inserting human CDR-transplanted antibody variable regions cassette-wise in the form of NotI-ApaI (H chain) and EcoRI-SplI (L chain) restriction fragments into a vector for human CDR-transplanted antibody expression, the ApaI and EcoRI restriction sites occurring in the rabbit .beta.-globin gene splicing and poly A signals of the plasmid pSE1UK1SEd1-3 were modified in the following manner.
Three .mu.g of the plasmid pBluescript SK(-) (Stratagene) was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the digestion reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, and the 3' cohesive ends resulting from ApaI digestion were rendered blunt using DNA Blunting Kit (Takara Shuzo), followed by ligation using DNA Ligation Kit (Takara Shuzo). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101. Thus was obtained a plasmid, pBSA, shown in FIG. 64. Furthermore, 3 .mu.g of the plasmid pBSA thus obtained was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of the restriction enzyme EcoRI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, and the 5' cohesive ends resulting from EcoRI digestion were rendered blunt using DNA Blunting Kit (Takara Shuzo), followed by ligation using DNA Ligation Kit (Takara Shuzo). The thuso-btained recombinant plasmid DNA solution was used to transform Escherichia coli HB101. Thus was obtained the plasmid pBSAE shown in FIG. 65.
Then, 3 .mu.g of the thus-obtained plasmid pBSAE was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT, 10 units of the restriction enzyme HindIII (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 20 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, and the solution was divided into two 10-.mu.l portions. To one portion, 10 units of the restriction enzyme SacII (Toyobo) was further added and, to the other, 10 units of the restriction enzyme KpnI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. Both the reaction mixtures were fractionated by agarose gel electrophoresis, whereby about 0.3 .mu.g each of a HindIII-SacII fragment (about 2.96 kb) and a KpnI-HindIII fragment (about 2.96 kb) were recovered.
Then, 3 .mu.g of the plasmid pSE1UK1SEd1-3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SacII (Toyobo) and 10 units of the restriction enzyme KonI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 50 mM sodium chloride and 1 mM DTT, 10 units of the restriction enzyme HindIII (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 0.2 .mu.g each of a HindIII-SacII fragment (about 2.42 kb) and a KpnI-HindIII fragment (about 1.98 kb) were recovered.
Then, 0.1 .mu.g of the thus-obtained HindIII-SacII fragment of pSE1UK1SEd1-3 and 0.1 .mu.g of the above HindIII-SacII fragment of pBSAE were dissolved in a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101 and, as a result, a plasmid, pBSH-S, shown in FIG. 66 was obtained. Further, 0.1 .mu.g of the above-mentioned KpnI-HindIII fragment of pSE1UK1SEd1-3 and 0.1 .mu.g of the above-mentioned KpnI-HindIII fragment of pBSAE were dissolved in a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSK-H shown in FIG. 67 was obtained.
Then, 3 .mu.g each of the thus-obtained plasmids pBSH-S and pBSK-H were respectively added to 10-.mu.l portions of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added to each mixture, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. Both the reaction mixtures were subjected to ethanol precipitation. With each precipitate, the 3' cohesive ends resulting from ApaI digestion were rendered blunt using DNA Blunting Kit (Takara Shuzo), followed by ligation using DNA Ligation Kit (Takara Shuzo). The thus-obtained recombinant DNA solution were used to transform Escherichia coli HB101, and the plasmids pBSH-SA and pBSK-HA shown in FIG. 68 were obtained.
Then, 5 .mu.g each of the thus-obtained plasmids pBSH-SA and pBSK-HA were respectively added to 10-.mu.l portions of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 1 unit of the restriction enzyme EcoRI (Takara Shuzo) was further added to each mixture, and the reaction was allowed to proceed at 37.degree. C. for 10 minutes for partial digestion. Both the reaction mixtures were subjected to ethanol precipitation. With each precipitate, the 5' cohesive ends resulting from EcoRI digestion were rendered blunt using DNA Blunting Kit (Takara Shuzo), followed by fractionation by agarose gel electrophoresis, whereby about 0.5 .mu.g each of a fragment about 5.38 kb in length and a fragment about 4.94 kb in length were recovered. The thus-recovered fragments (0.1 .mu.g each) were each dissolved in a total of 20 .mu.l of sterilized water and subjected to ligation treatment using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant DNA solutions were respectively used to transform Escherichia coli HB101, and the plasmids pBSH-SAE and pBSK-HAE shown in FIG. 69 were obtained.
Then, 3 .mu.g each of the thus-obtained plasmids pBSH-SAE and pBSK-HAE were respectively added to 10-.mu.l portions of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride, 100 mM sodium chloride and 1 mM DTT, 10 units of the restriction enzyme EcoRI (Takara Shuzo) was further added to each mixture, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. Both the reaction mixtures were subjected to ethanol precipitation. With each precipitate, the 5' cohesive ends resulting from EcoRI digestion were rendered blunt using DNA Blunting Kit (Takara Shuzo), followed by ligation using DNA Ligation Kit (Takara Shuzo). The thus-obtained recombinant plasmid DNA solutions were each used to transform Escherichia coli HB101, and two plasmids, pBSH-SAEE and pBSK-HAEE, shown in FIG. 70 were obtained. Ten .mu.g each of the thus-obtained plasmids were subjected to sequencing reaction according to the instructions attached to AutoRead Sequencing Kit (Pharmacia Biotech), followed by base sequence determination by electrophoresis on A.L.F. DNA Sequencer (Pharmacia Biotech), whereby it was confirmed that both the ApaI and EcoRI sites had disappeared as a result of the above modification.
(2) SalI restriction site introduction downstream from rabbit .beta.-globin gene splicing and poly A signals and SV40 early gene poly A signal
For making it possible to exchange the antibody H chain and L chain expression promoters of the human CDR-transplanted antibody expression vector each for an arbitrary promoter, a SalI restriction site was introduced into the plasmid pSE1UK1SEd1-3 downstream from the rabbit .beta.-globin gene splicing and poly A signals and from the SV40 early gene poly A signal in the following manner.
Three .mu.g of the plasmid pBSK-HAEE obtained in Paragraph 1 (1) of Example 3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme NaeI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 20 .mu.l of 50 mM Tris-hydrochloride buffer (pH 9.0) containing 1 mM magnesium chloride, 1 unit of alkaline phosphatase (E. coli C75, Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour for dephosphorylation at the 5' termini. The reaction mixture was further subjected to phenol-chloroform extraction and then to ethanol precipitation, and the precipitate was dissolved in 20 .mu.l of 10 mM Tris-hydrochloride buffer (pH 8.0) containing 1 mM disodium ethylenediaminetetraacetate (hereinafter briefly referred to as TE buffer). One .mu.l of said reaction solution and 0.1 .mu.g of a phosphorylated SaIlI linker (Takara Shuzo) were added to sterilized water to make a total volume of 20 .mu.l, followed by ligation treatment using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and a plasmid, pBSK-HAEESal, shown in FIG. 71 was obtained. Ten .mu.g of the plasmid thus obtained was subjected to sequencing reaction according to the instructions attached to AutoRead Sequencing Kit (Pharmacia Biotech), followed by electrophoresis on A.L.F. DNA Sequencer (Pharmacia Biotech) for base sequence determination, whereby it was confirmed that one SalI restriction site had been introduced downstream from the rabbit .beta.-globin gene splicing and poly A signals and from the SV40 early gene poly A signal.
(3) Modification of ApaI restriction site occurring in poly A signal of Herpes simplex virus thymidine kinase (hereinafter referred to as HSVtk) gene
The ApaI restriction site occurring in the HSVtk gene poly A signal downstream from the Tn5 kanamycin phosphotransferase gene of the plasmid pSE1UK1SEd1-3 was modified in the following manner.
Three .mu.g of the plasmid pBSA obtained in Paragraph 1 (1) of Example 3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SacII (Toyobo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme XhoI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of a SacII-XhoI fragment (about 2.96 kb) was recovered.
Then, 5 .mu.g of the plasmid pSE1UK1SEd1-3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SacII (Toyobo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme XhoI (Takara Shuzo) was further added, and the reaction was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of a SacII-XhoI fragment (about 4.25 kb) was recovered.
Then, 0.1 .mu.g of the above SacII-XhoI fragment of pBSA and the above SacII-XhoI fragment of pSE1UK1SEd1-3 were added to a total of 20 gl of sterilized water, followed by ligation using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSX-S shown in FIG. 72 was obtained.
Then, 3 .mu.g of the thus-obtained plasmid pBSX-S was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the 3' cohesive ends resulting from ApaI digestion were rendered blunt using DNA Blunting Kit (Takara Shuzo) and then ligation was carried out using DNA Ligation Kit (Takara Shuzo). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and a plasmid, pBSX-SA, shown in FIG. 73 was obtained. Ten .mu.g of the thus-obtained plasmid was subjected to sequencing reaction according to the instructions attached to AutoRead Sequencing Kit (Pharmacia Biotech), followed by electrophoresis on A.L.F. DNA Sequencer (Pharmacia Biotech) for base sequence determination, whereby it was confirmed that the ApaI restriction site in the HSVtk gene poly A signal had disappeared.
(4) Construction of human CDR-transplanted antibody L chain expression unit
A plasmid, pMohC.kappa., containing a human antibody .kappa. L chain constant region cDNA downstream from the promoter/enhancer of the Moloney mouse leukemia virus long terminal repeat and having a human CDR-transplanted antibody L chain expression unit allowing cassette-wise insertion thereinto of a human CDR-transplanted antibody L chain variable region was constructed in the following manner.
Three .mu.g of the plasmid pBluescript SK(-) (Stratagene) was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SacI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ClaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, and the cohesive ends resulting from SacI and ClaI digestion were rendered blunt using DNA Blunting Kit (Takara Shuzo), followed by fractionation by agarose gel electrophoresis, whereby about 1 .mu.g of a DNA fragment about 2.96 kb in length was recovered. A 0.1-.mu.g portion of the DNA fragment recovered was added to a total of 20 .mu.l of sterilized water and subjected to ligation reaction using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSSC shown in FIG. 74 was obtained.
Then, 3 .mu.g of the thus-obtained plasmid pBSSC was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme KpnI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme XhoI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of a KpnI-XhoI fragment (about 2.96 kb) was recovered.
Then, 5 .mu.g of the plasmid pAGE147 described in JP-A-6-205694 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme KpnI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme XhoI (Takara Shuzo) was further added, and the reaction was fractionated by agarose gel electrophoresis, whereby about 0.3 .mu.g of a KpnI-XhoI fragment (about 0.66 kb) containing the Moloney mouse leukemia virus long terminal repeat promoter/enhancer was recovered.
Then, 0.1 .mu.g of the KpnI-XhoI fragment of pBSSC and 0.1 .mu.g of the KpnI-XhoI fragment of pAGE147 each obtained as mentioned above were dissolved in a total of 20 .mu.l of sterilized water and subjected to ligation using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSMo shown in FIG. 75 was obtained.
Then, 3 .mu.g of the above plasmid pBSMo was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme KpnI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme HindIII (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of a KpnI-HindIII fragment (about 3.62 kb) was recovered.
Then, synthetic DNAs respectively having the base sequences shown in SEQ ID No:38 and SEQ ID No:39 were synthesized using an automatic DNA synthesizer (Applied Biosystems model 380A) To 15 .mu.l of sterilized water were added 0.3 .mu.g each of the thus-obtained synthetic DNAs, and the mixture was heated at 65.degree. C. for 5 minutes. The reaction mixture was allowed to stand at room temperature for 30 minutes and then 2 .mu.l of 10-fold concentrated buffer �500 mM Tris-hydrochloride (pH 7.6), 100 mM magnesium chloride, 50 mM DTT! and 2 .mu.l of 10 mM ATP were added, 10 units of T4 polynucleotide kinase was further added, and the reaction was allowed to proceed at 37.degree. C. for 30 minutes for phosphorylation of the 5' termini. To a total of 20 .mu.l of sterilized water were added 0.1 .mu.g of the above KpnI-HindIII fragment (3.66 kb) derived from the plasmid pBSMo and 0.05 .mu.g of the phsophorylated synthetic DNA pair, and ligation was effected using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSMoS shown in FIG. 76 was obtained. Ten .mu.g of the plasmid thus obtained was subjected to sequencing reaction according to the instructions attached to AutoRead Sequencing Kit (Pharmacia Biotech), followed by electrophoresis on A.L.F. DNA Sequencer (Pharmacia Biotech) for base sequence determination, whereby it was confirmed that the synthetic DNA pair had been introduced as desired.
Then, 3 .mu.g of the plasmid pChiIgLA1 described in JP-A-5-304989 was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and EcoRV (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of an EcoRI-EcoRV fragment (about 9.70 kb) was recovered.
Then, synthetic DNAs respectively having the base sequences shown in SEQ ID NO:40 and SEQ ID NO:41 were synthesized using an automatic DNA synthesizer (Applied Biosystems model 380A). To 15 .mu.l of sterilized water were added 0.3 .mu.g each of the thus-obtained synthetic DNAs, and the mixture was heated at 65.degree. C. for 5 minutes. The reaction mixture was allowed to stand at room temperature for 30 minutes. Then, 2 .mu.l of 10-fold concentrated buffer �500 mM Tris-hydrochloride (pH 7.6), 100 mM magnesium chloride, 50 mM DTT! and 2 .mu.l of 10 mM ATP were added, 10 units of T4 polynucleotide kinase was further added, and the reaction was allowed to proceed at 37.degree. C. for 30 minutes for phosphorylation of the 5' termini. To a total of 20 .mu.l of sterilized water were added 0.1 .mu.g of the above EcoRI-EcoRV fragment (9.70 kb) derived from the plasmid pChiIgLA1 and 0.05 .mu.g of the phsophorylated synthetic DNA, and ligation was effected using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pChiIgLA1S shown in FIG. 77 was obtained.
Then, 3 .mu.g of the plasmid pBSMoS obtained in the above manner was dissolved in 10 .mu.l of 20 mM Tris-hydrochloride buffer (pH 8.5) containing 100 mM potassium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme HpaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme EcoRI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of an HpaI-EcoRI fragment (about 3.66 kb) was recovered.
Then, 10 .mu.g of the plasmid pChiIgLA1S obtained as mentioned above was dissolved in 10 .mu.l of 20 mM Tris-acetate buffer (pH 7.9) containing 50 mM potassium acetate, 10 mM magnesium acetate, 1 mM DTT and 100 .mu.g/ml BSA, 10 units of the restriction enzyme NlaIV (New England BioLabs) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme EcoRI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 0.3 .mu.g of an NlaIV-EcoRI fragment (about 0.41 kb) was recovered.
Then, 0.1 .mu.g of the above HpaI-EcoRI fragment of pBSMoS and 0.1 .mu.g of the above NlaIV-EcoRI fragment of pChiIgLA1S were added to a total of 20 .mu.l of sterilized water, and ligation was effected using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pMohC.kappa. shown in FIG. 78 was obtained.
(5) Construction of human CDR-transplanted antibody H chain expression unit
A plasmid, pMohC.gamma.1, containing a human antibody .gamma.1 H chain constant region cDNA downstream from the pro-moter/enhancer of the Moloney mouse leukemia virus long terminal repeat and having a human CDR-transplanted antibody H chain expression unit allowing cassette-wise insertion thereinto of a human CDR-transplanted antibody H chain variable region was constructed in the following manner.
Three .mu.g of the plasmid pBSMo obtained in Paragraph 1 (4) of Example 3 was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme XhoI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 30 mM sodium acetate buffer (pH 5.0) containing 100 mM sodium chloride, 1 mM zinc acetate and 10% glycerol, 10 units of Mung bean nuclease (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 10 minutes. The reaction mixture was subjected to phenol-chloroform extraction and then to ethanol precipitation, the cohesive ends of the precipitate were rendered blunt using DNA Blunting Kit (Takara Shuzo) and ligation was effected using DNA Ligation Kit (Takara Shuzo). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSMoSal shown in FIG. 79 was obtained. A 10-.mu.g portion of the plasmid obtained was subjected to sequencing reaction according to the instructions attached to AutoRead Sequencing Kit (Pharmacia Biotech), followed by electrophoresis on A.L.F. DNA Sequencer (Pharmacia Biotech) for base sequence determination, whereby it was confirmed that the XhoI restriction site upstream of the Moloney mouse leukemia virus long terminal repeat promoter/enhancer had disappeared.
Then, 3 .mu.g of the plasmid pBSMoSal obtained as mentioned above was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme KpnI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme HindIII (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of a KpnI-HindIII fragment (about 3.66 kb) was recovered.
Then, synthetic DNAs respectively having the base sequences shown in SEQ ID NO:42 and SEQ ID NO:43 were synthesized using an automatic DNA synthesizer (Applied Biosystems model 380A). To 15 .mu.l of sterilized water were added 0.3 .mu.g each of the thus-obtained synthetic DNAs, and the mixture was heated at 65.degree. C. for 5 minutes. The reaction mixture was allowed to stand at room temperature for 30 minutes. Then, 2 .mu.l of 10-fold concentrated buffer �500 mM Tris-hydrochloride (pH 7.6), 100 mM magnesium chloride, 50 mM DTT! and 2 .mu.l of 10 mM ATP were added, 10 units of T4 polynucleotide kinase was further added, and the reaction was allowed to proceed at 37.degree. C. for 30 minutes for phosphorylation of the 5' termini. To a total of 20 .mu.l of sterilized water were added 0.1 .mu.g of the above KpnI-HindIII fragment (3.66 kb) derived from the plasmid pBSMoSal and 0.05 .mu.g of the phosphorylated synthetic DNA, and ligation was effected using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSMoSa1S shown in FIG. 80 was obtained. A 10-.mu.g portion of the thus-obtained plasmid was subjected to sequencing reaction according to the instructions attached to AutoRead Sequencing Kit (Pharmacia Biotech), followed by electrophoresis on A.L.F. DNA Sequencer (Pharmacia Biotech), for base sequence determination whereby it was confirmed that the synthetic DNA had been introduced as desired.
Then, 10 Ag of the plasmid pChiIgHB2 described in JP-A-5-304989 was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme Eco52I (Toyobo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 30 mM sodium acetate buffer (pH 5.0) containing 100 mM sodium chloride, 1 mM zinc acetate and 10% glycerol, 10 units of Mung bean nuclease (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 10 minutes. The reaction mixture was subjected to phenolchloroform extraction and then to ethanol precipitation, and the cohesive ends were rendered blunt using DNA Blunting Kit (Takara Shuzo). After ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 0.7 .mu.g of ApaI-blunt end fragment (about 0.99 kb) was recovered.
Then, 3 .mu.g of the plasmid pBluescript SK(-) (Stratagene) was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 33 mM Tris-acetate buffer (pH 7.9) containing 10 mM magnesium acetate, 66 mM potassium acetate, 0.5 mM DTT and 100 .mu.g/ml BSA, 10 units of the restriction enzyme SmaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of an ApaI-SmaI fragment (about 3.0 kb) was recovered.
Then, 0.1 .mu.g of the ApaI-blunt end fragment of pChiIgHB2 and 0.1 .mu.g of the ApaI-SmaI fragment of pbluescript SK(-), each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBShC.gamma.1 shown in FIG. 81 was obtained.
Then, 5 .mu.g of the above plasmid pBShC.gamma.1 was dissolved in 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApAI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SpeI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of an ApaI-SpeI fragment (about 1.0 kb) was recovered.
Then, 3 .mu.g of the plasmid pBSMoSalS obtained as mentioned above was dissolved in 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SpeI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of an ApaI-SpeI fragment (about 3.66 kb) was recovered.
Then, 0.1 .mu.g of the ApaI-SpeI fragment of pBShC.gamma.1 and 0.1 .mu.g of the ApaI-SpeI fragment of pBSMoSa1S, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pMohC.gamma.1 shown in FIG. 82 was obtained.
(6) Construction of tandem cassette type humanized antibody expression vector pKANTEX93
A tandem cassette type humanized antibody expression vector, pKANTEX93, was constructed using the various plasmids obtained in Paragraphs (1) through (5) of Example 3 in the following manner.
Three .mu.g of the plasmid PBSH-SAEE obtained in Paragraph 1 (1) of Example 3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme HindIII (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SalI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of a HindIII-SalI fragment (about 5.42 kb) was recovered.
Then, 5 .mu.g of the plasmid PBSK-HAEE obtained in Paragraph 1 (1) of Example 3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (ph 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme KpnI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme HindIII (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 0.8 .mu.g of a KpnI-HindIII fragment (about 1.98 kb) containing the rabbit .beta.-globin gene splicing and poly A signals, the SV40 early gene poly A signal and the SV40 early gene promoter was recovered.
Then, 5 .mu.g of the plasmid pMohC.gamma.1 obtained in Paragraph 1 (5) of Example 3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme KpnI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SalI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 0.8 .mu.g of a human CDR-transplanted antibody H chain expression unit-containing KpnI-SalI fragment (about 1.66 kb) was recovered.
Then, 0.1 .mu.g of the HindIII-SalI fragment of PBSH-SAEE, 0.1 .mu.g of the KpnI-HindIII fragment of pBSK-HAEE and 0.1 .mu.g of the KpnI-SalI fragment of pMohC.gamma.1, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated together using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pMo.gamma.1SP shown in FIG. 83 was obtained.
The, 3 .mu.g of the above plasmid pMo.gamma.1SP was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SalI (Takara Shuzo) and 10 units of the restriction enzyme XhoI were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of a SalI-XhoI fragment (about 9.06 kb) was recovered.
Then, 5 .mu.g of the plasmid pBSK-HAEESal obtained in Paragraph 1 (2) of Example 3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme KpnI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was. dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SalI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 0.7 .mu.g of a KpnI-SalI fragment (about 1.37 kb) containing the rabbit .beta.-globin gene splicing and poly A signals and the SV40 early gene poly A signal was recovered.
Then, 5 .mu.g of the plasmid pMohC.kappa. obtained in Paragraph 1 (4) of Example 3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1mM DTT, 10 units of the restriction enzyme KpnI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme XhoI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 0.7 .mu.g of a human CDR-transplanted antibody L chain expression unit-containing KpnI-XhoI fragment (about 1.06 kb) was recovered.
Then, 0.1 .mu.g of the SalI-XhoI fragment of pMo.gamma.1SP, 0.1 .mu.g of the KpnI-SalI fragment of pBSK-HAEESal and 0.1 .mu.g of the KpnI-XhoI fragment of pMohC.kappa., each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated together using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pMo.kappa..gamma.1SP shown in FIG. 84 was obtained.
Then, 3 .mu.g of the above plasmid pMo.kappa..gamma.1 SP was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme XhoI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 1 units of the restriction enzyme SacII (Toyobo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 10 minutes for partial digestion. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.2 .mu.g of a SacII-XhoI fragment (about 8.49 kb) was recovered.
Then, 3 .mu.g of the plasmid pBSX-SA obtained in Paragraph 1 (4) of Example 3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SacII (Toyobo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme XhoI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of a SacII-XhoI fragment (about 4.25 kb) was recovered.
Then, 0.1 .mu.g of the SacII-XhoI fragment of pMo.kappa..gamma.1SP and 0.1 .mu.g of the SacII-XhoI fragment of pBSX-SA, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pKANTEX93 shown in FIG. 85 was obtained.
2. Expression of Human Anti-GM.sub.2 Chimera Antibody Using Humanized Antibody Expression Vector pKANTEX93
Human anti-GM.sub.2 chimera antibody expression was effected using the humanized antibody expression vector pKANTEX93 mentioned above in Paragraph 1 of Example 3 in the following manner.
(1) Construction of plasmid pBSH3 containing mouse anti-GM.sub.2 antibody KM796 H chain variable region cDNA
Three .mu.g of the plasmid pBluescript SK(-) (Stratagene) was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units each of the restriction enzymes SacII (Toyobo) and KpnI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, and the precipitate was subjected to blunting treatment for rendering blunt the 3' cohesive ends resulting from the restriction enzyme digestion using DNA Blunting Kit (Takara Shuzo) and then to fractionation by agarose gel electrophoresis, and about 1 .mu.g of a DNA fragment about 2.95 kb in size was recovered.
Then, synthetic DNAs respectively having the base sequences shown in SEQ ID NO:44 and SEQ ID NO:45 were synthesized using an automatic DNA synthesizer (Applied Biosystems model 380A). To 15 .mu.l of sterilized water were added 0.3 .mu.g each of the synthetic DNAs obtained, and the mixture was heated at 65.degree. C. for 5 minutes. The reaction mixture was allowed to stand at room temperature for 30 minutes and then 2 .mu.l of 10-fold concentrated buffer �500 mM Tris-hydrochloride (pH 7.6), 100 mM magnesium chloride, 50 mM DTT! and 2 .mu.l of 10 mM ATP were added, 10 units of T4 polynucleotide kinase was further added, and the reaction was allowed to proceed at 37.degree. C. for 30 minutes for phosphorylating the 5' termini. To a total of 20 .mu.l of sterilized water were added 0.1 .mu.g of the DNA fragment (2.95 kb) derived from the plasmid pbluescript SK(-) and 0.05 .mu.g of the phosphorylated synthetic DNA, each obtained as mentioned above, followed by ligation to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSNA shown in FIG. 86 was obtained. Ten .mu.g of the plasmid obtained was subjected to sequencing reaction treatment according to the instructions attached to AutoRead Sequencing Kit (Pharmacia Biotech), followed by electrophoresis on A.L.F. DNA Sequencer (Pharmacia Biotech) for base sequence determination, whereby it was confirmed that the synthetic DNA had been introduced as desired.
Then, 3 .mu.g of the plasmid pBSNA obtained as mentioned above was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT, 100 .mu.g/ml BSA and 0.01% Triton X-100, 10 units of the restriction enzyme NotI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of a DNA fragment about 2.95 kb in size was recovered.
Then, 10 .mu.g of the plasmid pChi796HM1 obtained in Paragraph 7 (3) of Example 1 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT, 100 .mu.g/ml BSA and 0.0% Triton X-100, 10 units of the restriction enzyme NotI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.3 .mu.g of a DNA fragment about 0.45 kb in size was recovered.
Then, 0.1 .mu.g of the Apa-NotI fragment of PBSNA and 0.1 .mu.g of the Apa-NotI fragment of pChi796HM1, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSH3 shown in FIG. 87 was obtained.
(2) Construction of plasmid pBSL3 containing mouse anti-GM.sub.2 antibody KM796 L chain variable region cDNA
Three .mu.g of the plasmid pBluescript SK(-) (Stratagene) was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme KpnI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, and the precipitate was subjected to blunting treatment for rendering blunt the 3' cohesive ends resulting from KpnI digestion using DNA Blunting Kit (Takara Shuzo) and then to ethanol precipitation, the precipitate was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme SacI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of a DNA fragment about 2.95 kb in size was recovered.
Then, synthetic DNAs respectively having the base sequences shown in SEQ ID NO:46 and SEQ ID NO:47 were synthesized using an automatic DNA synthesizer (Applied Biosystems model 380A). To 15 .mu.l of sterilized water were added 0.3 .mu.g each of the synthetic DNAs obtained, and the mixture was heated at 65.degree. C. for 5 minutes. The reaction mixture was allowed to stand at room temperature for 30 minutes. Then, 2 .mu.l of 10-fold concentrated buffer �500 mM Tris-hydrochloride (pH 7.5), 100 mM magnesium chloride, 50 mM DTT! and 2 .mu.l of 10 mM ATP were added, 10 units of T4 polynucleotide kinase was further added, and the reaction was allowed to proceed at 37.degree. C. for 30 minutes for phosphorylating the 5' termini The, 0.1 .mu.g of the DNA fragment (2.95 kb) derived from the plasmid pbluescript SK(-) and 0.05 .mu.g of the phosphorylated synthetic DNA, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSES shown in FIG. 88 was obtained. Ten .mu.g of the plasmid obtained was subjected to sequencing reaction treatment according to the instructions attached to AutoRead Sequencing Kit (Pharmacia Biotech), followed by electrophoresis on A.L.F. DNA Sequencer (Pharmacia Biotech) for base sequence determination, whereby it was confirmed that the synthetic DNA had been introduced as desired.
Then, 3 .mu.g of the plasmid pBSES obtained as mentioned above was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of a DNA fragment about 2.95 kb in size was recovered.
The, 5 .mu.g of the plasmid pKM796L1 obtained in Paragraph 4 of Example 1 was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and AflIII (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.3 .mu.g of an EcoRI-AflIII fragment about 0.39 kb in size was recovered.
The, synthetic DNAs respectively having the base sequences shown in SEQ ID NO:48 and SEQ ID NO:49 were synthesized using an automatic DNA synthesizer (Applied Biosystems model 380A). To 15 .mu.l of sterilized water were added 0.3 .mu.g each of the synthetic DNAs obtained, and the mixture was heated at 65.degree. C. for 5 minutes. The reaction mixture was allowed to stand at room temperature for 30 minutes. Then, 2 .mu.l of 10-fold concentrated buffer �500 mM Tris-hydrochloride (pH 7.6), 100 mM magnesium chloride, 50 mM DTT! and 2 .mu.l of 10 mM ATP were added, 10 units of T4 polynucleotide kinase was further added, and the reaction was allowed to proceed at 37.degree. C. for 30 minutes for phosphorylating the 5' termini.
Then, 0.1 .mu.g of the pBSES-derived EcoRI-SplI fragment (2.95 kb), 0.1 .mu.g of the pKM796L1-derived EcoRI-AflIII fragment and 0.05 .mu.g of the phosphorylated synthetic DNA, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated together using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSL3 shown in FIG. 89 was obtained. Ten .mu.g of the plasmid obtained was subjected to sequencing reaction treatment according to the instructions attached to AutoRead Sequencing Kit (Pharmacia Biotech), followed by electrophoresis on A.L.F. DNA Sequencer (Pharmacia Biotech) for base sequence determination, whereby it was confirmed that the synthetic DNA had been introduced as desired.
(3) Construction of human anti-GM.sub.2 chimera antibody expression vector pKANTEX796
An human anti-GM.sub.2 chimera antibody expression vector, pKANTEX796, was constructed using the plasmid pKANTEX93 obtained in Paragraph 1 of Example 3 and the plasmids pBSH3 and pBSL3 respectively obtained in Paragraph 2 (1) and (2) of Example 3, in the following manner.
Three .mu.g of the plasmid pBSH3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT, 100 .mu.g/ml BSA and 0.01% Triton X-100, 10 units of the restriction enzyme NotI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.3 .mu.g of an ApaI-NotI fragment about 0.46 kb in size was recovered.
Then, 3 .mu.g of the plasmid pKANTEX93 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT, 100 .mu.g/ml BSA and 0.01% Triton X-100, 10 units of the restriction enzyme NotI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, whereby about 1 .mu.g of an ApaI-NotI fragment about 12.75 kb in size was recovered.
Then, 0.1 .mu.g of the pBSH3-derived ApaI-NotI fragment and 0.1 .mu.g of the pKANTEX93-derived ApaI-NotI fragment, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pKANTEX796H shown in FIG. 90 was obtained.
Then, 3 .mu.g of the plasmid pBSL3 was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.3 .mu.g of an EcoRI-SplI fragment about 0.4 kb in size was recovered.
Then, 3 .mu.g of the plasmid pKANTEX796H was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of an EcoRI-SplI fragment about 13.20 kb in size was recovered.
Then, 0.1 .mu.g of the pBSL3-derived EcoRI-SplI fragment and 0.1 .mu.g of the pKANTEX796H-derived EcoRI-SplI fragment, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pKANTEX796 shown in FIG. 91 was obtained.
(4) Expression of human anti-GM.sub.2 chimera antibody by pKANTEX796
According to the procedure described in Paragraph 11 of Example 1, pKANTEX796 was introduced into YB2/0 (ATCC CRL 1581) cells and, as a result of selection by means of G418 (0.5 mg/ml) and MTX (200 nM), a cell line capable of producing about 1 to 2 .mu.g/ml of human anti-GM.sub.2 chimera antibody was obtained. It was confirmed that efficient and stable humanized antibody expression is possible using expression vector pKANTEX93.
3. Transient Humanized Antibody Expression in COS-7 (ATCC CRL 1651) Cells
For enabling more rapid activity evaluation of various versions of human CDR-transplanted anti-GM.sub.2 antibody, transient expression of human anti-GM.sub.2 chimera antibody expression was caused in COS-7 cells by the Lipofectamine method using pKANTEX796 and a variant thereof in the following manner.
(1) Construction of variant of pKANTEX796
Since transient antibody expression in animal cells is dependent on the copy number of an expression vector introduced, it was supposed that an expression vector smaller in size would show a higher expression efficiency. Therefore, a smaller humanized antibody expression vector, pT796, was constructed by deleting a region supposedly having no effect on humanized antibody expression from pKANTEX796 in the following manner.
Thus, 3 .mu.g of the plasmid pKANTEX796 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme HindIII (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was dissolved in 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme MluI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, and the 5' cohesive ends resulting from the restriction enzyme digestion were rendered blunt using DNA Blunting Kit (Takara Shuzo). The reaction mixture was fractionated by agarose gel electrophoresis and about 1 .mu.g of a DNA fragment about 9.60 kb in size was recovered. A 0.1-.mu.g portion of the thus-recovered DNA fragment was added to a total of 20 .mu.l of sterilized water and subjected to ligation treatment using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pT796 shown in FIG. 92 was obtained.
(2) Transient expression of human anti-GM.sub.2 chimera antibody using pKANTEX796 and pT796
A 1.times.10.sup.5 cells/ml suspension of COS-7 cells was distributed in 2-ml portions into wells of a 6-well plate (Falcon) and cultured overnight at 37.degree. C. Two .mu.g of pKANTEX796 or pT796 was added to 100 .mu.l of OPTI-MEM medium (Gibco), a solution prepared by adding 10 .mu.l of LIPOFECTAMINE reagent (Gibco) to 100 .mu.l of OPTI-MEM medium (Gibco) was further added, and the reaction was allowed to proceed at room temperature for 40 minutes to cause DNA-liposome complex formation. The COS-7 cells cultured overnight were washed twice with 2 ml of OPTI-MEM medium (Gibco), the complex-containing solution was added, and the cells were cultured at 37.degree. C. for 7 hours. Then, the solution was removed, 2 ml of DMEM medium (Gibco) containing 10% FCS was added to each well, and the cells were cultured at 37.degree. C. After 24 hours, 48 hours, 72 hours, 96 hours and 120 hours of cultivation, the culture supernatant was recovered and, after concentration procedure as necessary, evaluated for human anti-GM.sub.2 chimera antibody activity in the culture supernatant by the ELISA method described in Paragraph 11 of Example 1. The results are shown in FIG. 93. As shown in FIG. 93, higher levels of transient human anti-GM.sub.2 chimera antibody expression was observed with pT796 as compared with pKANTEX796. For pT796, the level of expression was highest at 72 to 96 hours, the concentration being about 30 ng/ml (in terms of GM.sub.2 binding activity). The above results indicate that construction of a pKANTEX93-derived vector having a reduced size and introduction thereof into COS-7 cells make it possible to make activity evaluation of expression vector-derived humanized antibodies in a transient expression system. Furthermore, for close activity comparison of various versions of human CDR-transplanted anti-GM.sub.2 antibody as mentioned hereinafter, the ELISA method described below under (3) was used to determine antibody concentrations in transient expression culture supernatants.
(3) Determination by ELISA of humanized antibody concentrations in transient expression culture supernatants
A solution prepared by 400-fold dilution of goat anti-human IgG (.gamma. chain) antibody (Igaku Seibutugaku Kenkyusho) with PBS was distributed in 50-.mu.l portions into wells of a 96-well microtiter plate and allowed to stand overnight at 4.degree. C. for binding to the wells. After removing the antibody solution, blocking was effected with 100 .mu.l of PBS containing 1% BSA at 37.degree. C. for 1 hour. Fifty .mu.l of a transient expression culture supernatant or purified human anti-GM.sub.2 chimera antibody was added thereto and allowed to react at room temperature for 1 hour. Thereafter, the solution was removed, the wells were washed with PBS, and 50 .mu.l of a solution prepared by 500-fold dilution of peroxidase-labeled mouse anti-human .kappa. L chain antibody (Zymet) with PBS was added and allowed to react at room temperature for 1 hour. After washing with PBS, 50 .mu.l of an ABTS substrate solution �prepared by dissolving 550 mg of 2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt in 0.1M citrate buffer (pH 4.2) and adding, just before use, 1 .mu.l/ml of hydrogen peroxide! was added for causing color development, and the OD.sub.415 was measured.
4. Production of human CDR-transplanted anti-GM.sub.2 antibody using humanized antibody expression vector pKANTEX93
A human CDR-transplanted anti-GM.sub.2 antibody higher in GM.sub.2 binding activity than the human CDR-transplanted anti-GM.sub.2 antibody described in Example 2 was produced in the following manner.
(1) Modification of human CDR-transplanted anti-GM.sub.2 antibody H chain variable region described in Paragraph 1 (1) of Example 2
DNAs coding for some versions of the human CDR-transplanted anti-GM.sub.2 antibody H chain variable region described in Example 2 as derived by replacing several amino acids in regions other than the CDR (framework; hereinafter referred to as FR) with original mouse antibody amino acids were constructed in the following manner. Based on a computer model for the variable region of mouse KM796, those amino acid residues that were expected to contribute to restoration of antigen-binding activity as a result of mutation were selected as the amino acid residues to be mutated.
First, DNAs respectively having the base sequences of SEQ ID NO:50 and SEQ ID NO:51 were synthesized using an automatic DNA synthesize (Applied Biosystems model 380A).
Then, a version (version 2) of human CDR-transplanted antibody H chain variable region shown in SEQ ID NO:52 and having mutation in positions 78 (threonine in lieu of glutamine), 79 (alanine in lieu of phenylalanine) and 80 (tyrosine in lieu of serine) was constructed in the same manner as in Paragraph 1 (1) of Example 2 using a synthetic DNA of SEQ ID NO:50 in lieu of the synthetic DNA of SEQ ID NO:27.
Then, another version (version 4) of human CDR-transplanted antibody H chain variable region shown in SEQ ID NO:53 and having mutations in positions 27 (tyrosine in lieu of phenylalanine), 30 (threonine in lieu of serine), 40 (serine in lieu of proline) and 41 (histidine in lieu of proline) was constructed in the same manner as in Paragraph 1 (1) of Example 2 using a synthetic DNA of SEQ ID NO:51 in lieu of the synthetic DNA of SEQ ID NO:25.
(2) Construction of human CDR-transplanted anti-GM.sub.2 antibody H chain variable region using known common human antibody H chain variable region
According to Kabat et al. (Kabat E. A. et al., "Sequences of Proteins of Immunological Interest", US Dept. of Health and Human Services, 1991), known human antibody H chain variable regions are classifiable into subgroups I to III (HSG I to III) based on the homology of their FR regions, and common sequences have been identified for respective subgroups. Therefore, a human CDR-transplanted anti-GM.sub.2 antibody H chain variable region was constructed based on those common sequences. First, for selecting common sequences to serve as the base, the homology was examined between the FR of the mouse KM796 H chain variable region and the common sequence FR of the human antibody H chain variable region of each subgroup (Table 3).
TABLE 3______________________________________Homology (%) between mouse KM796 H chain variable regionFR and human antibody H chain variable region commonsequence FRHSG I HSG II HSG III______________________________________72.1 52.9 58.6______________________________________
As a result, it was confirmed that subgroup I shows the greatest similarity. Thus, based on the common sequences of subgroup I, a human CDR-transplanted anti-GM.sub.2 antibody H chain variable region was constructed by the PCR method in the following manner.
Synthetic DNAs respectively having the base sequences of SEQ ID NO:54 through SEQ ID NO:59 were synthesized using an automatic DNA synthesizer (Applied Systems model 380A). The DNAs synthesized were added, each to a final concentration of 0.1 .mu.M, to 50 .mu.l of 10 mM Tris-hydrochloride buffer (pH 8.3) containing 50 mM potassium chloride, 1.5 mM magnesium chloride, 0.00% gelatin, 200 .mu.M dNTP, 0.5 .mu.M M13 primer RV (Takara Shuzo), 0.5 .mu.M M13 primer M4 (Takara Shuzo) and 2 units of TaKaRa Taq DNA polymerase, the mixture was covered with 50 .mu.l of mineral oil, a DNA thermal cycler (Perkin Elmer model PJ480) was loaded with the mixture, and 30 PCR cycles (2 minutes at 94.degree. C., 2 minutes at 55.degree. C. and 2 minutes at 72.degree. C. per cycle) were conducted. The reaction mixture was purified using QIAquick PCR Purification Kit (Qiagen) and then made into a solution in 30 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 50 mM Tris-hydrochloride (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT, 100 .mu.g/ml BSA and 0.0% Triton X-100, 10 units of the restriction enzyme NotI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.2 .mu.g of an ApaI-NotI fragment about 0.44 kb in size was recovered.
Then, 3 .mu.g of the plasmid pBSH3 obtained in Paragraph 2 (1) of Example 3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT, 100 .mu.g/ml BSA and 0.01% Triton X-100, 10 units of the restriction enzyme NotI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agrose gel electrophoresis, and about 1 .mu.g of an ApaI-NotI fragment about 2.95 kb in size was recovered.
Then, 0.1 .mu.g of the ApaI-NotI fragment of the human CDR-transplanted anti-GM.sub.2 antibody H chain variable region and 0.1 .mu.g of the ApaI-NotI fragment of pBSH3, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101. Plasmid DNAs were prepared from 10 transformant clones and their base sequences were determined. As a result, a plasmid, pBSH10, shown in FIG. 94 and having the desired base sequence was obtained. The amino acid sequence and base sequence of the human CDR-transplanted anti-GM.sub.2 antibody H chain variable region contained in pBSH10 are shown in SEQ ID NO:60. In the amino acid sequence of the thus-constructed human CDR-transplanted anti-GM.sub.2 antibody H chain variable region, the amino acids in positions 67, 72, 84 and 98 in the FR as selected based on a computer model for the variable region are those amino acids found in the mouse KM796 H chain variable region. This is for the purpose of retaining the antigenbinding capacity of mouse KM796.
(3) Modification of human CDR-transplanted anti-GM.sub.2 antibody L chain variable region described in Paragraph 1 (2) of Example 2
First, a DNA having the base sequence of SEQ ID NO:61 was synthesized using an automatic DNA synthesizer (Applied Biosystems model 380A), and a human CDR-transplanted anti-GM.sub.2 antibody L chain variable region cDNA with a 3' terminus capable of pairing with the restriction enzyme SplI was constructed by following the same reaction procedure as in Paragraph 1 (2) of Example 2 using the synthetic DNA in lieu of the synthetic DNA of SEQ ID NO:35.
Then, 3 .mu.g of the plasmid pBSL3 obtained in Paragraph 2 (2) of Example 3 was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of an EcoRI-SplI fragment about 2.95 kb in size was recovered.
Then, 0.1 .mu.g of the EcoRI-SplI fragment of the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region obtained as mentioned above and 0.1 .mu.g of the above EcoRI-SplI fragment of pBSL3 were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSL16 shown in FIG. 95 was obtained.
Then, DNAs coding for certain versions of the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region contained in the above plasmid pBSL16 were constructed by replacing a certain number of amino acids in the FR with original mouse antibody amino acids by mutagenesis by means of PCR in the following manner (FIG. 96). Based on a computer model for the variable region of mouse KM796, those amino acid residues that were expected to contribute to restoration of antigen-binding activity as a result of mutation were selected as the amino acid residues to be mutated.
Antisense and sense DNA primers for introducing mutations were synthesized using an automatic DNA synthesizer (Applied Biosystems model 380A). A first PCR reaction was conducted in the same manner as in Paragraph 4 (2) of Example 3 using a final concentration each of 0.5 .mu.M of M13 primer RV (Takara Shuzo) and the antisense DNA primer and of M13 primer M4 (Takara Shuzo) and the sense DNA primer, with 1 ng of pBSL16 as the template. Each reaction mixture was purified using QIAquick PCR Purification Kit (Qiagen) with elution with 20 .mu.l of 10 mM Tris-hydrochloride (pH 8.0). Using 5 .mu.l of each eluate, a second PCR reaction was conducted in the same manner as in Paragraph 4 (2) of Example 3. The reaction mixture was purified using QIAaquick PCR Purification Kit (Qiagen) and then made into a solution in 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.2 .mu.g of an EcoRI-SplI fragment (about 0.39 kb) of each mutant version of the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region was recovered.
Then, 0.1 .mu.g of the above EcoRI-SplI fragment of each mutant version of the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region and 0.1 .mu.g of the EcoRI-SplI fragment of pBSL3 were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and a plasmid DNA was prepared from a transformant clone, and the base sequence of said plasmid was determined. In this way, plasmids respectively containing a base sequence having a desired mutation or mutations were obtained.
Thus, a plasmid, pBSLV1, containing version 1, shown in SEQ ID NO:64, of the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region was obtained following the above procedure using the synthetic DNA of SEQ ID NO:62 as the mutant antisense primer and the synthetic DNA of SEQ ID NO:63 as the mutant sense primer. In the amino acid sequence of the version 1 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region, the amino acid in position 15 in the FR is that amino acid found in the mouse KM796 L chain variable region. This is for the purpose of retaining the antigen-binding capacity of mouse KM796.
A plasmid, pBSLV2, containing version 2, shown in SEQ ID NO:67, of the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region was obtained following the above procedure using the synthetic DNA of SEQ ID NO:65 as the mutant antisense primer and the synthetic DNA of SEQ ID NO:66 as the mutant sense primer. In the amino acid sequence of the version 2 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region, the amino acid in positions 46 in the FR is that amino acid found in the mouse KM796 L chain variable region. This is for the purpose of retaining the antigen-binding capacity of mouse KM796.
A plasmid, pBSLV3, containing version 3, shown in SEQ ID NO:70, of the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region was obtained following the above procedure using the synthetic DNA of SEQ ID NO:68 as the mutant antisense primer and the synthetic DNA of SEQ ID NO:69 as the mutant sense primer. In the amino acid sequence of the version 3 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region, the amino acids in position 79 and 82 in the FR are those amino acids found in the mouse KM796 L chain variable region. This is for the purpose of retaining the antigen-binding capacity of mouse KM796.
Then, a plasmid, pBSLV1+2, containing a human CDR-transplanted anti-GM.sub.2 antibody L chain variable region having both the version 1 and version 2 mutations was constructed in the following manner.
Three .mu.g of the plasmid pBSLV1 obtained as mentioned above was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and HindIII (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.2 .mu.g of an EcoRI-HindIII fragment about 0.20 kb in size was recovered.
Then, 3 .mu.g of the plasmid pBSLV2 obtained as mentioned above was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and HindIII (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of an EcoRI-HindIII fragment about 3.2 kb in size was recovered.
Then, 0.1 .mu.g of the EcoRI-HindIII fragment of pBSLV1 and 0.1 .mu.g of the EcoRI-HindIII fragment of pBSLV2, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSLV1+2 shown in FIG. 97 was obtained.
Then, the PCR reaction procedure mentioned above was followed using 1 ng of the plasmid pBSLV1+2 obtained as mentioned above as the template, a synthetic DNA having the base sequence of SEQ ID NO:71 as the mutant antisense primer and a synthetic DNA having the base sequence of SEQ ID NO:72 as the mutant sense primer, whereby a plasmid, pBSLV4, containing a version 4 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region set forth in SEQ ID NO:73 was obtained. In the amino acid sequence of the version 4 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region, the amino acids in positions 15, 46, 69, 70 and 71 in the FR are those amino acids that are found in the mouse KM796 L chain variable region. This is for the purpose of retaining the antigen-binding capacity of mouse KM796.
Then, the PCR reaction procedure mentioned above was followed using 1 ng of the plasmid pBSLV1+2 obtained as mentioned above as the template, a synthetic DNA having the base sequence of SEQ ID NO:74 as the mutant antisense primer and a synthetic DNA having the base sequence of SEQ ID NO:75 as the mutant sense primer, whereby a plasmid, pBSLV8, containing a version 8 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region set forth in SEQ ID NO:76 was obtained. In the amino acid sequence of the version 8 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region, the amino acids in positions 15, 46, 69, 70, 71, 76, 77 and 78 in the FR are those amino acids that are found in the mouse KM796 L chain variable region. This is for the purpose of retaining the antigen-binding capacity of mouse KM796.
Then, the PCR reaction procedure mentioned above was followed using 1 ng of the plasmid pBSLV4 obtained as mentioned above as the template, a synthetic DNA having the base sequence of SEQ ID NO:77 as the mutant antisense primer and a synthetic DNA having the base sequence of SEQ ID NO:78 as the mutant sense primer, whereby a plasmid, pBSLm-2, containing a version Lm-2 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region set forth in SEQ ID NO:79 was obtained. In the amino acid sequence of the version Lm-2 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region, the amino acids in positions 15, 35, 46, 69, 70 and 71 in the FR are those amino acids that are found in the mouse KM796 L chain variable region. This is for the purpose of retaining the antigen-binding capacity of mouse KM796.
Then, the PCR reaction procedure mentioned above was followed using 1 ng of the plasmid pBSLV4 obtained as mentioned above as the template, a synthetic DNA having the base sequence of SEQ ID NO:80 as the mutant antisense primer and a synthetic DNA having the base sequence of SEQ ID NO:81 as the mutant sense primer, whereby a plasmid, pBSLm-8, containing a version Lm-8 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region set forth in SEQ ID NO:82 was obtained. In the amino acid sequence of the version Lm-8 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region, the amino acids in positions 15, 46, 69, 70, 71, 72 and 77 in the FR are those amino acids that are found in the mouse KM796 L chain variable region. This is for the purpose of retaining the antigen-binding capacity of mouse KM796.
Then, a plasmid, pBSLm-28, containing a human CDR-transplanted anti-GM.sub.2 antibody L chain variable region having both the version Lm-2 and version Lm-8 mutations was constructed in the following manner.
Three .mu.g of the plasmid pBSLm-2 obtained as mentioned above was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme EcoRI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units of the restriction enzyme XbaI (Takara Shuzo) was further added, and the reaction as allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.2 .mu.g of an EcoRI-XbaI fragment about 0.24 kb in size was recovered.
Then, 3 .mu.g of the plasmid pBSLm-8 obtained as mentioned above was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme EcoRI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 50 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units of the restriction enzyme XbaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of an EcoRI-XbaI fragment about 3.16 kb in size was recovered.
Then, 0.1 .mu.g of the EcoRI-XbaI fragment of pBSLm-2 and 0.1 .mu.g of the EcoRI-XbaI fragment of pBSLm-8, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pBSLm-28 shown in FIG. 98 was obtained. The version Lm-28 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region contained in the plasmid pBSLm-28 is shown in SEQ ID NO:83. In the amino acid sequence of the version Lm-28 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region thus constructed, the amino acids in positions 15, 35, 46, 69, 70, 71, 72 and 77 are those amino acids that are found in the mouse KM796 L chain variable region. This is for the intended purpose of retaining the antigen-binding capacity of mouse KM796.
(4) Construction of human CDR-transplanted anti-GM.sub.2 antibody L chain variable region using known common human antibody L chain variable region
According to Kabat et al. (Kabat E. A. et al., "Sequences of Proteins of Immunological Interest", US Dept. of Health and Human Services, 1991), known human antibody L chain variable regions are classifiable into subgroups I to IV based on the homology of their FR regions, and common sequences have been identified for respective subgroups. Therefore, a human CDR-transplanted anti-GM.sub.2 antibody L chain variable region was constructed based on those common sequences. First, for selecting common sequences to serve as the base, the homology was examined between the FR of the mouse KM796 L chain variable region and the common sequence FR of the human antibody L chain variable region of each subgroup (Table 4).
TABLE 4______________________________________Homology (%) between mouse KM796 L chain variable region FRand human antibody L chain variable region common sequence FRHSG I HSG II HSG III HSG IV______________________________________70.0 65.0 68.8 67.5______________________________________
As a result, it was confirmed that subgroup I shows the greatest similarity. Thus based on the common sequence of subgroup I, a human CDR-transplanted anti-GM.sub.2 antibody L chain variable region was constructed by the PCR method in the following manner.
Synthetic DNAs respectively having the base sequences of SEQ ID NO:84 through SEQ ID NO:89 were synthesized using an automatic DNA synthesizer (Applied Systems model 380A). The DNAs synthesized were added, each to a final concentration of 0.1 .mu.M, to 50 .mu.l of 10 mM Tris-hydrochloride buffer (pH 8.3) containing 50 mM potassium chloride, 1.5 mM magnesium chloride, 0.001% gelatin, 200 .mu.M dNTP, 0.5 .mu.M M13 primer RV (Takara Shuzo), 0.5 .mu.M M13 primer M4 (Takara Shuzo) and 2 units of TaKaRa Taq DNA polymerase. The mixture was covered with 50 .mu.l of mineral oil, a DNA thermal cycler (Perkin Elmer model PJ480) was loaded with the mixture, and 30 PCR cycles (2 minutes at 94.degree. C., 2 minutes at 55.degree. C. and 2 minutes at 72.degree. C. per cycle) were conducted. The reaction mixture was purified using QIAquick PCR Purification Kit (Qiagen) and then made into a solution in 30 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electro-phoresis, and about 0.2 .mu.g of an EcoRI-SplI fragment about 0.39 kb in size was recovered.
Then, 0.1 .mu.g of the above EcoRI-SplI fragment of the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region and 0.1 .mu.g of the EcoRI-SplI fragment of pBSL3 were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101. Plasmid DNAs were prepared from 10 transformant clones and their base sequences were determined. As a result, a plasmid, PBSHSGL, shown in FIG. 99 and having the desired base sequence was obtained. The amino acid sequence and base sequence of the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region contained in pBSHSGL are shown in SEQ ID NO:90. In the amino acid sequence of the thus-constructed human CDR-transplanted anti-GM.sub.2 antibody L chain variable region, the amino acids in positions 4, 11, 15, 35, 42, 46, 69, 70, 71, 77 and 103 in the FR as selected based on a computer model for the variable region are those amino acids found in the mouse KM796 L chain variable region. This is for the intended purpose of retaining the antigen-binding capacity of mouse MK796.
(5) Activity evaluation of mutant versions of human CDR-transplanted anti-GM.sub.2 antibody in terms of transient expression
Various mutant version human CDR-transplanted anti-GM.sub.2 antibodies composed of the human CDR-transplanted anti-GM.sub.2 antibody H chain and L chain variable regions constructed in Paragraphs (1) through (4) of Example 3 and having varying mutations were evaluated for activity in terms of transient expression in the following manner.
First, for evaluating the human CDR-transplanted anti-GM.sub.2 antibody H chain variable regions having varying mutations, expression vectors, pT796HCDRHV2, pT796HCDRHV4 and pT796HCDRH10, were constructed by replacing the mouse H chain variable region of the human anti-GM.sub.2 chimera antibody transient expression vector pT796 obtained in Paragraph 3 (1) of Example 3 with the human CDR-transplanted anti-GM.sub.2 antibody H chain variable regions having varying mutations, in the following manner. For comparison, an expression vector, pT796HCDR was constructed by replacing the mouse H chain variable region of pT796 with the human CDR-transplanted anti-GM.sub.2 antibody H chain variable region obtained in Paragraph 1 (1) of Example 1.
Three .mu.g of the plasmid pT796 was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, lmM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of an EcoRI-SplI fragment about 9.20 kb in size was recovered.
Then, 3 .mu.g of the plasmid pBSL16 obtained in Paragraph 4 (3) of Example 3 was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.3 .mu.g of an EcoRI-SplI fragment about0.39 kb in size was recovered.
Then, 0.1 .mu.g of the EcoRI-SplI fragment of pT796 and 0.1 .mu.g of the EcoRI-SplI fragment of pBSL16, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pT796LCDR shown in FIG. 100 was obtained.
Then, 3 .mu.g of the above plasmid pT796LCDR was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT, 100 .mu.g/ml BSA and 0.01% Triton X-100, 10 units of the restriction enzyme NotI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of an ApaI-NotI fragment about 9.11 kb in size was recovered.
Then, 0.1 .mu.g of the human CDR-transplanted anti-GM.sub.2 antibody H chain variable region obtained in Paragraph 1 (1) of Example 2 or the mutant version 2 or 4 human CDR-transplanted anti-GM.sub.2 antibody H chain variable region obtained in Paragraph 4 (1) of Example 3 and 0.1 .mu.g of the ApaI-NotI fragment of pT796LCDR were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). Each recombinant plasmid DNA solution thus obtained was used to transform Escherichia coli HB101. The plasmids pT796HLCDR, pT796HLCDRHV2 and pT796HLCDRHV4 shown in FIG. 101 were obtained. Then, 3 .mu.g of the plasmid pBSH10 obtained in Paragraph 4 (2) of Example 3 was added to 10 .mu.l of 10 mM Tris-hydrochloride buffer (pH 7.5) containing 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme ApaI (Takara Shuzo) was further added, and the restriction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT, 100 .mu.g/ml BSA and 0.01% Triton X-100, 10 units of the restriction enzyme NotI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.3 .mu.g of an ApaI-NotI fragment about 0.44 kb in size was recovered.
Then, 0.1 .mu.g of the ApaI-NotI fragment of pBSM10 and 0.1 .mu.g of the ApaI-NotI fragment of pT796LCDR were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). The thus-obtained recombinant plasmid DNA solution was used to transform Escherichia coli HB101, and the plasmid pT796HLCDRH10 shown in FIG. 102 was obtained.
Then, 3 .mu.g each of the plasmids pT796HLCDR, pT796HLCDRHV2, pT796HLCDRHV4 and pT796HLCDRH10 were respectively added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. Each reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of an EcoRI-SplI fragment about 9.15 kb in size was recovered.
Then, 5 .mu.g of the plasmid pBSL3 obtained in Paragraph 2 (2) of Example 3 was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 0.4 .mu.g of an EcoRI-SplI fragment about 0.39 kb in size was recovered.
Then, 0.1 .mu.g of the EcoRI-SplI fragment of each of pT796HLCDR, pT796HLCDRHV2, pT796HLCDRHV4 and pT796HLCDRH10 and 0.1 .mu.g of the EcoRI-SplI fragment of pBSL3 were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go DNA Ligase (Pharmacia Biotech). Each recombinant plasmid DNA solution thus obtained was used to transform Escherichia coli HB101. In this way, the plasmids pT796HCDR, pT796HCDRHV2, pT796HCDRHV4 and pT796HCDRH10 shown in FIG. 103 were obtained.
Then, 2 .mu.g each of the plasmids pT796HCDR, pT796HCDRHV2, pT796HCDRHV4 and pT796HCDRH10 thus obtained were used for transient human CDR-transplanted anti-GM.sub.2 antibody expression and for culture supernatant human CDR-transplanted anti-GM.sub.2 antibody activity evaluation by the procedures described in Paragraph 3 (2) and (3) of Example 3, respectively. After introduction of each plasmid, the culture supernatant was recovered at 72 hours, and the GM.sub.2 -binding activity and antibody concentration in the culture supernatant were determined by ELISA and the relative activity was calculated with the activity of the positive control chimera antibody taken as 100%. The results are shown in FIG. 104.
The results revealed that the amino acid mutations alone in mutant versions 2 and 4 have little influence on the restoration of the antigen-binding activity of the human CDR-transplanted anti-GM.sub.2 antibody but that the use of the pBSH10-derived human CDR-transplanted antibody H chain variable region constructed based on the known human antibody H chain variable region common sequence, contributes to the restoration of the antigen-binding activity.
In view of the above results, the human CDR-transplanted anti-GM.sub.2 antibody H chain variable region constructed based on the known human antibody H chain variable region common sequence as shown in SEQ ID NO:60 was selected as a novel human CDR-transplanted anti-GM.sub.2 antibody H chain variable region.
Then, for evaluating the human CDR-transplanted anti-GM.sub.2 antibody L chain variable regions having varying variations, expression vectors, pT796HLCDRLV1, pT796HLCDRLV2, pT796HLCDRLV3, pT796HLCDRLV4, pT796HLCDRLV8, pT796HLCDRLm-2, pT796HLCDRLm-8, pT796HLCDRLm-28 and pT796HLCDRHSGL, were constructed in the following manner by replacing the mouse L chain variable region of the vector pT796HCDRH10 for transient human CDR-transplanted anti-GM.sub.2 antibody expression obtained as mentioned above with the human CDR-transplanted anti-GM.sub.2 antibody L chain variable regions having varying mutations.
Thus, 3 .mu.g of the plasmid pT796HCDRH10 was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of an EcoRI-SplI fragment about 9.15 kb in size was recovered.
Then, 3 .mu.g of the plasmid pBSLV1, pBSLV2, pBSLV3, pBSLV4, pBSLV8, pBSLm-2, pBSLm-8, pBSLm-28 or PBSHSGL obtained in Paragraph (3) or (4) of Example 3 was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride, 1 mM DTT and 100 .mu.g/ml BSA, 10 units each of the restriction enzymes EcoRI (Takara Shuzo) and SplI (Takara Shuzo) were further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. Each reaction mixture was fractionated by agarose gel electrophoresis, and about 0.3 .mu.g of an EcoRI-SplI fragment about 0.39 kb in size was recovered.
Then, 0.1 .mu.g of the EcoRI-SplI fragment of the pT796HCDRH10 and 0.1 .mu.g of the EcoRI-SplI fragment of each mutant version human CDR-transplanted anti-GM.sub.2 antibody L chain variable region were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). Each recombinant plasmid DNA solution thus obtained was used to transform Escherichia coli HB101. In this way, the plasmids pT796HLCDRLV1, pT796HLCDRLV2, pT796HLCDRLV3, pT796HLCDRLV4, pT796HLCDRLV8, pT796HLCDRLm-2, pT796HLCDRLm-8, pT796HLCDRLm-28 and pT796HLCDRHSGL were obtained as shown in FIG. 105.
Then, 2 .mu.g each of the thus-obtained plasmids pT796HLCDRLV1, pT796HLCDRLV2, pT796HLCDRLV3, pT796HLCDRLV4, pT796HLCDRLV8, pT796HLCDRLm-2, pT796HLCDRLm-8, pT796HLCDRLm-28 and pT796HLCDRHSGL and of the plasmid pT796HLCDR described in Example 2 and capable of expressing human CDR-transplanted anti-GM.sub.2 antibody were used for transient human CDR-transplanted anti-GM.sub.2 antibody expression and for culture supernatant human CDR-transplanted anti-GM.sub.2 antibody activity evaluation by the procedures described in Paragraph 3 (2) and (3) of Example 3, respectively. After introduction of each plasmid, the culture supernatant was recovered at 72 hours, and the GM.sub.2 -binding activity and antibody concentration in the culture supernatant were determined by ELISA and the relative activity was calculated with the activity of the positive control chimera antibody taken as 100%. The results are shown in FIG. 106.
The results revealed that the amino acid mutations alone in mutant versions 1, 2, 3, 4 and 8 have little influence on the restoration of the antigen-binding activity of the human CDR-transplanted anti-GM.sub.2 antibody but that the amino acid mutations in mutant versions Lm-2 and Lm-8 contributes to the restoration of the antigen-binding activity. Furthermore, version Lm-28 having both the amino acid mutations of Lm-2 and Lm-8 showed a high level of antigen-biding activity almost comparable to that of the chimera antibody, revealing that those amino acids mutated in producing Lm-28 were very important from the antigen-binding activity viewpoint.
In view of the above results, the version Lm-28 human CDR-transplanted anti-GM.sub.2 antibody L chain variable region shown in SEQ ID NO:83 was selected as a first novel human CDR-transplanted anti-GM.sub.2 antibody L chain variable region.
It was further revealed that the antigen-binding activity can be restored when the pBSHSGL-derived human CDR-transplanted anti-GM.sub.2 antibody L chain variable region, namely the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region constructed based on the known human antibody L chain variable region common sequence, is used.
In view of the above result, the human CDR-transplanted anti-GM.sub.2 antibody L chain variable region constructed based on the known human antibody L chain variable region common sequence as set forth in SEQ ID NO:90 was selected as a second novel human CDR-transplanted anti-GM.sub.2 antibody L chain variable region.
It is to be noted that in those human CDR-transplanted anti-GM.sub.2 antibody L chain variable regions that showed high binding activity against GM.sub.2, certain amino acid residues which cannot be specified by deduction from known human CDR-transplanted antibody production examples have been replaced with amino acids found in the mouse L chain variable region. Thus, obviously, it was very important, in human CDR-transplanted anti-GM.sub.2 antibody production, to identify these amino acid residues.
Furthermore, the fact that the human CDR-transplanted anti-GM.sub.2 antibodies having those human CDR-transplanted anti-GM.sub.2 antibody H chain and L chain variable regions based on the known human antibody variable region common sequences showed high antigen binding activity is proof of the usefulness of the present process in human CDR-transplanted antibody production.
(6) Acquisition of cell lines for stable production of human CDR-transplanted anti-GM.sub.2 antibodies
Based on the results of Paragraph 4 (5) of Example 3, two cell lines, KM8966 and KM8967, capable of stably expressing KM8966, which has the amino acid sequence set forth in SEQ ID NO:60 as the H chain variable region and the amino acid sequence set forth in SEQ ID NO:83 as the L chain variable region, and KM8967, which has the amino acid sequence set forth in SEQ ID NO:60 as the H chain variable region and the amino acid sequence set forth in SEQ ID NO:90 as the L chain variable region, respectively as human CDR-transplanted anti-GM.sub.2 antibodies having higher antigen-binding activity than the human CDR-transplanted anti-GM.sub.2 antibody described in Example 2 were obtained in the following manner.
Three .mu.g each of the plasmids pT796HLCDRLm-28 and pT796HLCDRHSGL obtained in Paragraph 4 (5) of Example 3 were respectively added to 10 .mu.l of 20 mM Tris-hydrochloride buffer (pH 8.5) containing 100 mM potassium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme BamHI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. Each reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme XhoI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. Each reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of a BamHI-XhoI fragment about 4.93 kb in size was recovered.
Then, 3 .mu.g of the plasmid pKANTEX93 obtained in Paragraph 1 of Example 3 was added to 10 .mu.l of 20 mM Tris-hydrochloride buffer (pH 8.5) containing 100 mM potassium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme BamHI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was subjected to ethanol precipitation, the precipitate was added to 10 .mu.l of 50 mM Tris-hydrochloride buffer (pH 7.5) containing 100 mM sodium chloride, 10 mM magnesium chloride and 1 mM DTT, 10 units of the restriction enzyme XhoI (Takara Shuzo) was further added, and the reaction was allowed to proceed at 37.degree. C. for 1 hour. The reaction mixture was fractionated by agarose gel electrophoresis, and about 1 .mu.g of a BamHI-XhoI fragment about 8.68 kb in size was recovered.
Then, 0.1 .mu.g of the BamHI-XhoI fragment of pT796HLCDRLm-28 or pT796HLCDRHSGL and 0.1 .mu.g of the BamHI-XhoI fragment of pKANTEX93, each obtained as mentioned above, were added to a total of 20 .mu.l of sterilized water and ligated to each other using Ready-To-Go T4 DNA Ligase (Pharmacia Biotech). Each recombinant plasmid DNA solution thus obtained was used to transform Escherichia coli HB101. In this way, the plasmids pKANTEX796HLCDRLm-28 and pKANTEX796HLCDRHSGL shown in FIG. 107 were obtained.
Then, 4 .mu.g each of the above plasmids pKANTEX796HLCDRLm-28 and pKANTEX796HLCDRHSGL were respectively used to transform YB2/0 (ATCC CRL 1581) cells according to the procedure described in Paragraph 11 of Example 1 and, after final selection using G418 (0.5 mg/ml) and MTX (200 nM), a transformant cell line, KM8966, capable of producing about 40 .mu.g/ml of KM8966, i.e. the pKANTEX796HLCDRLm-28-derived human CDR-transplanted anti-GM.sub.2 antibody, and a transformant cell line, KM8967, capable of producing about 30 .mu.g/ml of KM8966, i.e. the pKANTEX796HLCDRHSGL-derived human CDR-transplanted anti-GM.sub.2 antibody, were obtained.
(7) Purification of human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967
The transformant cell lines KM8966 and 8967 obtained in Paragraph 4 (6) of Example 3 were respectively suspended in GIT medium (Nippon Pharmaceutical) containing 0.5 mg/ml G418 and 200 nM MTX and, according to the procedure of Paragraph 11 of Example 1, 18 mg of purified human CDR-transplanted anti-GM.sub.2 antibody KM8966 and 12 mg of purified KM8967 were obtained each from about 0.5 liter of culture fluid. Three .mu.g each of the purified human CDR-transplanted anti-GM.sub.2 antibodies obtained and the human anti-GM.sub.2 chimera antibody KM966 were subjected to electrophoresis by the known method �Laemli, Nature, 227, 680 (1979)! for molecular weight determination. The results are shown in FIG. 108. As shown, under reducing conditions, both antibody H chains showed a molecular weight of about 50 kilodaltons and both antibody L chains showed a molecular weight of about 25 kilodaltons. Expression of H and L chains of correct molecular weights was thus confirmed. Under non-reducing conditions, both human CDR-transplanted anti-GM.sub.2 antibodies showed a molecular weight of about 150 kilodaltons and it was thus confirmed that antibodies each composed of two H chains and two L chains and having a correct size had been expressed. Furthermore, the H and L chains of each human CDR-transplanted anti-GM.sub.2 antibody were analyzed for N-terminal amino acid sequence by automatic Edman degradation using a protein sequencer (Applied Biosystems model 470A), whereby an amino acid sequence deducible from the base sequence of the variable region DNA constructed was revealed.
5. In vitro reactivity of human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967 against GM.sub.2
The human anti-GM.sub.2 chimera antibody KM966 and the purified human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967 were tested for reactivity against GM.sub.2 by ELISA as described in Paragraph 11 of Example 1. The results are shown in FIG. 109. GM.sub.2 (N-acetyl-GM.sub.2) used was purified from cultured cell line HPB-ALL �Oboshi et al., Tanpakushitsu, Kakusan & Koso (Protein, Nucleic acid & Enzyme), 23, 697 (1978) ! in accordance with the known method �J. Biol. Chem., 263, 10915 (1988)!. As shown, it was found that the purified human CDR-transplanted anti-GM.sub.2 antibody KM8966 exerted the binding activity comparable to that of the human anti-GM.sub.2 chimera antibody KM966. On the other hand, the binding activity of purified human CDR-transplanted anti-GM.sub.2 antibody KM8967 was about 1/4 to 1/5 of that of the human anti-GM.sub.2 chimera antibody KM966.
6. Reaction specificity of human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967
The human anti-GM.sub.2 chimera antibody KM966 and the human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967 were tested for reactivity against the gangliosides GM.sub.1, N-acetyl-GM.sub.2, N-glycolyl-GM.sub.2, N-acetyl-GM.sub.3, N-glycolyl-GM.sub.3, GD.sub.1a, GD.sub.1b (Iatron), GD.sub.2, GD.sub.3 (Iatron) and GQ.sub.1b (Iatron) by ELISA as described in Paragraph 11 of Example 1. The results are shown in FIG. 110. GM.sub.1 and GD.sub.1a were purified from bovine brain, N-acetyl-GM.sub.2 from cultured cell line HPB-ALL �Oboshi et al., Tanpakushitsu, Kakusan & Koso (Protein, Nucleic acid & Enzyme), 23, 697 (1978)!, N-glycolyl-GM.sub.2 and N-glycolyl-GM.sub.3 from mouse liver, N-acetyl-GM.sub.3 canine erythrocytes, and GD.sub.2 from cultured cell line IMR32 (ATCC CCL127), respectively by the per se known method �J. Biol. Chem., 263, 10915 (1988)!. Each antibody was used in a concentration of 10 .mu.g/ml.
As shown in FIG. 110, it was confirmed that the human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967 react specifically with GM.sub.2 (N-acetyl-GM.sub.2 and N-glycolyl-GM.sub.2) like the human anti-GM.sub.2 chimera antibody KM966.
7. Reactivity of human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967 against cancer cells
The human lung small cell carcinoma culture cell line SBC-3 (JCRB 0818) (1.times.10.sup.6 cells) was suspended in PBS, the suspension was placed in a microtube (TREF) and centrifuged (1200 rpm, 2 minutes). To the thus-washed cells was added 50 .mu.l (50 .mu.g/ml) of the human anti-GM.sub.2 chimera antibody KM966 or the purified human CDR-transplanted anti-GM.sub.2 antibody KM8966 or KM8967, followed by stirring and 1 hour of standing at 4.degree. C. After the above reaction step, the cells were washed three times with PBS, each time followed by centrifugation. Then, 20 .mu.l of fluorescein isocyanate-labeled protein A (30-fold dilution, Boehringer Mannheim) was added and, after stirring, the reaction was allowed to proceed at 4.degree. C. for 1 hour. Thereafter, the cells were washed three times with PBS, each time followed by centrifugation, then further suspended in PBS and subjected to analysis using a flow cytometer, EPICS Elite (Coulter). In a control run, the above procedure was followed without addition of the human CDR-transplanted anti-GM.sub.2 antibody and analyzed. The results are shown in FIG. 111. It was found that the purified human CDR-transplanted anti-GM.sub.2 antibodies KM8966 and KM8967 strongly reacted with the human lung small cell carcinoma culture cell line SBC-3 like the human anti-GM.sub.2 chimera antibody KM966.
The results shown indicate that, like the human chimera antibodies, the human CDR-transplanted anti-GM.sub.2 antibodies are useful in the diagnosis and treatment of human cancer, among others.
While the invention has been described in detail and with reference to specific examples thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.
__________________________________________________________________________# SEQUENCE LISTING- (1) GENERAL INFORMATION:- (iii) NUMBER OF SEQUENCES: 103- (2) INFORMATION FOR SEQ ID NO:1:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 449 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide19..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: BY SIMILA - #RITY WITH KNOWN SEQUENCE OR TO AN#CONSENSUS ESTABLISHED- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 31..35 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 1"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 50..66 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 2"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 99..109 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 3"- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:- CTCCACAGTC CCTGAAGACA CTGACTCTAA CC ATG GGA TGG AGC - # TGG ATC TTT 53#Met Gly Trp Ser Trp Ile Phe15- CTC TTC CTC CTG TCA GGA ACT GCA GGT GTC CT - #C TCT GAG GTC CAG CTG 101Leu Phe Leu Leu Ser Gly Thr Ala Gly Val Le - #u Ser Glu Val Gln Leu# 1- CAG CAG TCT GGA CCT GAG CTG GTG AAG CCT GG - #G GCT TCA GTG AAG ATA 149Gln Gln Ser Gly Pro Glu Leu Val Lys Pro Gl - #y Ala Ser Val Lys Ile# 20- TCC TGC AAG GCT TCT GGA TAC ACA TTC ACT GA - #C TAC AAC ATG GAC TGG 197Ser Cys Lys Ala Ser Gly Tyr Thr Phe Thr As - #p Tyr Asn Met Asp Trp# 35- GTG AAG CAG AGC CAT GGA AAG AGC CTT GAG TG - #G ATT GGA TAT ATT TAT 245Val Lys Gln Ser His Gly Lys Ser Leu Glu Tr - #p Ile Gly Tyr Ile Tyr# 50- CCT AAC AAT GGT GGT ACT GGC TAC AAC CAG AA - #G TTC AAG AGC AAG GCC 293Pro Asn Asn Gly Gly Thr Gly Tyr Asn Gln Ly - #s Phe Lys Ser Lys Ala# 65- ACA TTG ACT GTA GAC AAG TCC TCC AGC ACA GC - #C TAC ATG GAG CTC CAC 341Thr Leu Thr Val Asp Lys Ser Ser Ser Thr Al - #a Tyr Met Glu Leu His# 80- AGC CTG ACA TCT GAG GAC TCT GCA GTC TAT TA - #C TGT GCA ACC TAC GGT 389Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr Ty - #r Cys Ala Thr Tyr Gly#100- CAT TAC TAC GGC TAC ATG TTT GCT TAC TGG GG - #C CAA GGG ACT CTG GTC 437His Tyr Tyr Gly Tyr Met Phe Ala Tyr Trp Gl - #y Gln Gly Thr Leu Val# 115# 449Thr Val Ser Ala 120- (2) INFORMATION FOR SEQ ID NO:2:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 393 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: BY SIMILA - #RITY WITH KNOWN SEQUENCE TO TO AN#CONSENSUS ESTABLISHED- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 1"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 2"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 3"- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:#TTC CTG CTA ATC AGT 48AG ATT TTC AGC Met His Phe Gln Val Gln Il - #e Phe Ser Phe Leu Leu Ile Ser10- GCC TCA GTC ATA ATG TCC AGA GGA CAA ATT GT - #T CTC ACC CAG TCT CCA 96Ala Ser Val Ile Met Ser Arg Gly Gln Ile Va - #l Leu Thr Gln Ser Pro# 5 1- GCA ATC ATG TCT GCA TCT CCA GGG GAG AAG GT - #C ACC ATA ACC TGC AGT 144Ala Ile Met Ser Ala Ser Pro Gly Glu Lys Va - #l Thr Ile Thr Cys Ser# 20- GCC AGC TCA AGT GTA AGT TAC ATG CAC TGG TT - #C CAG CAG AAG CCA GGC 192Ala Ser Ser Ser Val Ser Tyr Met His Trp Ph - #e Gln Gln Lys Pro Gly# 40- ACT TCT CCC AAA CTC TGG ATT TAT AGC ACA TC - #C AAC CTG GCT TCT GGA 240Thr Ser Pro Lys Leu Trp Ile Tyr Ser Thr Se - #r Asn Leu Ala Ser Gly# 55- GTC CCT GCT CGC TTC AGT GGC AGT GGA TCT GG - #G ACC TCT TAC TCT CTC 288Val Pro Ala Arg Phe Ser Gly Ser Gly Ser Gl - #y Thr Ser Tyr Ser Leu# 70- ACA ATC AGC CGA ATG GAG GCT GAA GAT GCT GC - #C ACT TAT TAC TGC CAG 336Thr Ile Ser Arg Met Glu Ala Glu Asp Ala Al - #a Thr Tyr Tyr Cys Gln# 85- CAA AGG AGT AGT TAC CCG TAC ACG TTC GGA GG - #G GGG ACC AAG CTG GAA 384Gln Arg Ser Ser Tyr Pro Tyr Thr Phe Gly Gl - #y Gly Thr Lys Leu Glu# 100# 393Ile Lys Arg105- (2) INFORMATION FOR SEQ ID NO:3:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 443 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide19..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: BY SIMILA - #RITY WITH KNOWN SEQUENCE OR TO AN#CONSENSUS ESTABLISHED- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 31..35 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 1"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 55..66 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 2"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 99..107 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISEHD CONSENSUS#/product= "HYPERVARIABLE REGION 3"- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:- CTCCACAGTC CCTGAAGACA CTGACTCTAA CC ATG GGA TGG AGC - # TGG ATC TTT 53#Met Gly Trp Ser Trp Ile Phe15- CTC TTC CTC CTG TCA GGA ACT GCA GGT GTC CT - #C TCT GAG GTC CAG CTG 101Leu Phe Leu Leu Ser Gly Thr Ala Gly Val Le - #u Ser Glu Val Gln Leu# 1- CAG CAG TCT GGA CCT GAG CTG GTG AAG CCT GG - #G GCT TCA GTG AAG ATA 149Gln Gln Ser Gly Pro Glu Leu Val Lys Pro Gl - #y Ala Ser Val Lys Ile# 20- TCC TGC AAG GCT TCT GGA TAC ACA TTC ACT GA - #C TAC AAC ATG GAC TGG 197Ser Cys Lys Ala Ser Gly Tyr Thr Phe Thr As - #p Tyr Asn Met Asp Trp# 35- GTG AAG CAG AGC CAT GGA AAG AGC CTT GAG TG - #G ATT GGA TAT ATT TAT 245Val Lys Gln Ser His Gly Lys Ser Leu Glu Tr - #p Ile Gly Tyr Ile Tyr# 50- CCT AAC AAT GGT GGT ACT GGC TAC AAC CAG AA - #G TTC AAG AGC AAG GCC 293Pro Asn Asn Gly Gly Thr Gly Tyr Asn Gln Ly - #s Phe Lys Ser Lys Ala# 65- ACA TTG ACT GTA GAC AAG TCC TCC AGC ACA GC - #C TAC ATG GAG CTC CAC 341Thr Leu Thr Val Asp Lys Ser Ser Ser Thr Al - #a Tyr Met Glu Leu His# 80- AGC CTG ACA TCT GAG GAC TCT GCA GTC TAT TA - #C TGT GCA AGA GCG GGG 389Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr Ty - #r Cys Ala Arg Ala Gly#100- AGG TAT TAC TAC GCC TGG GAC TGG GGC CAA GG - #G ACT CTG GTC ACT GTC 437Arg Tyr Tyr Tyr Ala Trp Asp Trp Gly Gln Gl - #y Thr Leu Val Thr Val# 115# 443Ser Ala- (2) INFORMATION FOR SEQ ID NO:4:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 405 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA to mRNA- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide (B) LOCATION: 10..66 (C) IDENTIFICATION METHOD: BY SIMILA - #RITY WITH KNOWN SEQUENCE OR TO AN#CONSENSUS ESTABLISHED- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 157..171 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 1"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 214..261 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 2"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 358..369 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 3"- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:- CATCACAGC ATG GCT GTC CTG GTG CTG TTG CTC TGC - # CTG GTG ACA TTT 48#Leu Leu Leu Cys Leu Val Thr Phe10- CCA AGC TGT GTC CTG TCC CAA GTG CAG CTG AA - #G GAG TCA GGA CCT GGT 96Pro Ser Cys Val Leu Ser Gln Val Gln Leu Ly - #s Glu Ser Gly Pro Gly# 10- CTG GTG CAG CCC TCA CAG ACC CTG TCC CTC AC - #C TGC ACT GTC TCT GGG 144Leu Val Gln Pro Ser Gln Thr Leu Ser Leu Th - #r Cys Thr Val Ser Gly# 25- TTC TCA TTA ACC AGC TAT ACT GTA AGC TGG GT - #T CGC CAG CCT CCA GGA 192Phe Ser Leu Thr Ser Tyr Thr Val Ser Trp Va - #l Arg Gln Pro Pro Gly# 40- AAG GGT CTG GAG TGG ATT GCA GCA ATA TCA AG - #T GGT GGA AGC ACA TAT 240Lys Gly Leu Glu Trp Ile Ala Ala Ile Ser Se - #r Gly Gly Ser Thr Tyr# 55- TAT AAT TCA GCT CTC AAA TCA CGA CTG AGC AT - #C AGC AGG GAC ACC TCC 288Tyr Asn Ser Ala Leu Lys Ser Arg Leu Ser Il - #e Ser Arg Asp Thr Ser# 70- AAG AGC CAA GTT TTC TTA AAA ATG AAC AGT CT - #G CAA ACT GAA GAC ACA 336Lys Ser Gln Val Phe Leu Lys Met Asn Ser Le - #u Gln Thr Glu Asp Thr# 90- GCC ATG TAC TTC TGT GCC CCT TCT GAG GGG GC - #C TGG GGC CAA GGA GTC 384Ala Met Tyr Phe Cys Ala Pro Ser Glu Gly Al - #a Trp Gly Gln Gly Val# 105# 405 TCA GAGMet Val Thr Val Ser Ser Glu 110- (2) INFORMATION FOR SEQ ID NO:5:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 402 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA to mRNA- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide (B) LOCATION: 19..78 (C) IDENTIFICATION METHOD: BY SIMILA - #RITY WITH KNOWN SEQUENCE OR TO AN#CONSENSUS ESTABLISHED- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 148..180 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABILSHED CONSENSUS#/product= "HYPERVARIABLE REGION 1"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 226..246 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 2"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 343..369 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 3"- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:#TTA GGG CTG CTG 51 ATG GCT CCA GTC CAG CTC#Leu Leuet Ala Pro Val Gln Leu Leu Gly10- CTG ATT TGG CTC CCA GCC ATG AGA TGT GAC AT - #C CAG ATG ACC CAG TCT 99Leu Ile Trp Leu Pro Ala Met Arg Cys Asp Il - #e Gln Met Thr Gln Ser#1 5- CCT TCA TTC CTG TCT GCA TCT GTG GGA GAC AG - #A GTC ACT ATC AAC TGC 147Pro Ser Phe Leu Ser Ala Ser Val Gly Asp Ar - #g Val Thr Ile Asn Cys# 20- AAA GCA AGT CAG AAT ATT AAC AAG TAC TTA AA - #C TGG TAT CAG CAA AAG 195Lys Ala Ser Gln Asn Ile Asn Lys Tyr Leu As - #n Trp Tyr Gln Gln Lys# 35- CTT GGA GAA GCT CCC AAA CGC CTG ATA TAT AA - #T ACA AAC AAT TTG CAA 243Leu Gly Glu Ala Pro Lys Arg Leu Ile Tyr As - #n Thr Asn Asn Leu Gln# 55- ACG GGC ATT CCA TCA AGG TTC AGT GGC AGT GG - #A TCT GGT ACA GAT TAC 291Thr Gly Ile Pro Ser Arg Phe Ser Gly Ser Gl - #y Ser Gly Thr Asp Tyr# 70- ACA CTC ACC ATC AGC AGC CTG CAG CCT GAA GA - #T TTT GCC ACA TAT TTC 339Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu As - #p Phe Ala Thr Tyr Phe# 85- TGC TTG CAG CAT AAT AGT TTT CCG AAC ACG TT - #T GGA GCT GGG ACC AAG 387Cys Leu Gln His Asn Ser Phe Pro Asn Thr Ph - #e Gly Ala Gly Thr Lys# 100# 402 GGLeu Glu Leu Lys Arg 105- (2) INFORMATION FOR SEQ ID NO:6:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 15 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:# 15 ACAsp Tyr Asn Met Asp 1 5- (2) INFORMATION FOR SEQ ID NO:7:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 51 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:- TAT ATT TAT CCT AAC AAT GGT GGT ACT GGC TA - #C AAC CAG AAG TTC AAG 48Tyr Ile Tyr Pro Asn Asn Gly Gly Thr Gly Ty - #r Asn Gln Lys Phe Lys# 15# 51Ser- (2) INFORMATION FOR SEQ ID NO:8:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 33 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:# 33T TAC TAC GGC TAC ATG TTT GCT TA - #CTyr Gly His Tyr Tyr Gly Tyr Met Phe Ala Ty - #r# 10- (2) INFORMATION FOR SEQ ID NO:9:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 30 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA(genomic)- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9:# 30 GT GTA AGT TAC ATG CACSer Ala Ser Ser Ser Val Ser Tyr Met His# 10- (2) INFORMATION FOR SEQ ID NO:10:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 21 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:10:#21 TG GCT TCTSer Thr Ser Asn Leu Ala Ser 1 5- (2) INFORMATION FOR SEQ ID NO:11:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 27 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11:# 27 GT TAC CCG TAC ACGGln Gln Arg Ser Ser Tyr Pro Tyr Thr 1 5- (2) INFORMATION FOR SEQ ID NO:12:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 31 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12:# 31 CA GCC TCC ACC AAG GGC CVal Thr Val Ser Ala Ala Ser Thr Lys Gly# 10- (2) INFORMATION FOR SEQ ID NO:13:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 51 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13:#AAA CGA ACT GTG GCT 46 CTG GAA ATA Thr Phe Gly Gly Gly Thr Lys Leu Glu I - #le Lys Arg Thr Val Ala# 15# 51Ala- (2) INFORMATION FOR SEQ ID NO:14:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 43 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14:- CAA GGA GTC ATG GTC ACA GTC TCG AGC GCC TC - #C ACC AAG GGC# 42Gln Gly Val Met Val Thr Val Ser Ser Ala Se - #r Thr Lys Gly# 10# 43- (2) INFORMATION FOR SEQ ID NO:15:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 51 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:15:#AAA CGA ACT GTG GCT 46 CTT GAG CTC Thr Phe Gly Ala Gly Thr Lys Leu Glu L - #eu Lys Arg Thr Val Ala# 15# 51Ala- (2) INFORMATION FOR SEQ ID NO:16:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 812 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (vi) ORIGINAL SOURCE: (B) STRAIN: HYBRIDOMA K - #M50- (ix) FEATURE: (A) NAME/KEY: TATA.sub.-- - #signal (B) LOCATION: 261..267- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:16:- AAAGTCAGAC AACTTTGTAG AGTAGGTTCT ATCAATCCTA CTGCAATCCA AC - #ATCACTGA 60- GGACAAATGT TTATACTGAG GAACCTGGTC TTGTGTGATA CGTACTTTCT GT - #GGGAAGCA 120- GATACGCACT CTCATGTGGC TCCTGAATTT CCCATCACAG AATGATACAT CT - #TGAGTCCT 180- AAAATTTAAG TACACCATCA GTGTCAGCAC CTGGTGAGGA AATGCAAATC TC - #TCCTGGAT 240- CCACCCAACC TTGGGTTGAA AAGCCAAAGC TGGGCCTGGG TACTCACTGG TG - #TGCAGCC 299- ATG GAC AGG CTT ACT TCC TCA TTC CTA CTG CT - #G ATG GTC CCT GCA 34 - #4Met Asp Arg Leu Thr Ser Ser Phe Leu Leu Le - #u Met Val Pro Ala- TGTGAGTACC AAAGCTTCCT AAGTGATGAA CTGTTCTATC CTCACCTGTT CA - #AACCTGAC 404- CTCCTCCCCT TTGATTTCTC CACAG AT GTC CTG TCT CAG G - #TT ACT CTG AAA 455#Val Thr Leu Lysl Leu Ser Gln# 5 1- GAA TCT GGC CCT GGG ATA TTG CAG CCC TCC CA - #G ACC CTC AGT CTG ACT 503Glu Ser Gly Pro Gly Ile Leu Gln Pro Ser Gl - #n Thr Leu Ser Leu Thr# 20- TGC TCT TTC TCT GGG TTT TCA CTG AGC ACT TA - #T GGT ATG TGT GTG GGC 551Cys Ser Phe Ser Gly Phe Ser Leu Ser Thr Ty - #r Gly Met Cys Val Gly# 35- TGG ATT CGT CAG TCT TCA GGG AAG GGT CTG GA - #G TGG CTG GCA AAC GTT 599Trp Ile Arg Gln Ser Ser Gly Lys Gly Leu Gl - #u Trp Leu Ala Asn Val# 50- TGG TGG AGT GAT GCT AAG TAC TAC AAT CCA TC - #T CTG AAA AAC CGG CTC 647Trp Trp Ser Asp Ala Lys Tyr Tyr Asn Pro Se - #r Leu Lys Asn Arg Leu# 65- ACA ATC TCC AAG GAC ACC TCC AAC AAC CAA GC - #A TTC CTC AAG ATC ACC 695Thr Ile Ser Lys Asp Thr Ser Asn Asn Gln Al - #a Phe Leu Lys Ile Thr# 85- AAT ATG GAC ACT GCA GAT ACT GCC ATA TAC TA - #C TGT GCT GGG AGA GGG 743Asn Met Asp Thr Ala Asp Thr Ala Ile Tyr Ty - #r Cys Ala Gly Arg Gly# 100- GCT ACG GAG GGT ATA GTG AGC TTT GAT TAC TG - #G GGC CAC GGA GTC ATG 791Ala Thr Glu Gly Ile Val Ser Phe Asp Tyr Tr - #p Gly His Gly Val Met# 115# 812 GGTAAGVal Thr Val Ser Ser 120- (2) INFORMATION FOR SEQ ID NO:17:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 46 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:17:# 46ATA TCAAGCTTGT CGACTCTAGA GGTACC- (2) INFORMATION FOR SEQ ID NO:18:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 29 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:18:# 29 GCAG CCACAGTTC- (2) INFORMATION FOR SEQ ID NO:19:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 408 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA to mRNA- (vi) ORIGINAL SOURCE: (B) STRAIN: HYBRIDOMA K - #M-641- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide (B) LOCATION: 25..84 (C) IDENTIFICATION METHOD: BY SIMILA - #RITY WITH KNOWN SEQUENCE OR TO AN#CONSENSUS ESTABLISHED- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:19:- AATTCGGCAC GAGTCAGCCT GGAC ATG ATG TCC TCT GCT C - #AG TTC CTT GGT 51#Gln Phe Leu Glyt Ser Ser Ala15- CTC CTG TTG CTC TGT TTT CAA GGT ACC AGA TG - #T GAT ATC CAG ATG ACA 99Leu Leu Leu Leu Cys Phe Gln Gly Thr Arg Cy - #s Asp Ile Gln Met Thr# 5 1- CAG ACT GCA TCC TCC CTG CCT GCC TCT CTG GG - #A GAC AGA GTC ACC ATC 147Gln Thr Ala Ser Ser Leu Pro Ala Ser Leu Gl - #y Asp Arg Val Thr Ile# 20- AGT TGC AGT GCA AGT CAG GAC ATT AGT AAT TA - #T TTA AAC TGG TAT CAA 195Ser Cys Ser Ala Ser Gln Asp Ile Ser Asn Ty - #r Leu Asn Trp Tyr Gln# 35- CAG AAA CCA GAT GGA ACT GTT AAA CTC CTG AT - #C TTT TAC TCA TCA AAT 243Gln Lys Pro Asp Gly Thr Val Lys Leu Leu Il - #e Phe Tyr Ser Ser Asn# 50- TTA CAC TCG GGA GTC CCA TCA AGG TTC AGT GG - #C GGT GGG TCC GGG ACA 291Leu His Ser Gly Val Pro Ser Arg Phe Ser Gl - #y Gly Gly Ser Gly Thr# 65- GAT TAT TCT CTC ACC ATC AGC AAC CTG GAG CC - #T GAA GAT ATT GCC ACT 339Asp Tyr Ser Leu Thr Ile Ser Asn Leu Glu Pr - #o Glu Asp Ile Ala Thr# 85- TAC TTT TGT CAT CAG TAT AGT AAG CTT CCG TG - #G ACG TCC GGT GGA GGC 387Tyr Phe Cys His Gln Tyr Ser Lys Leu Pro Tr - #p Thr Ser Gly Gly Gly# 100# 408 AAA CGGThr Lys Leu Glu Ile Lys Arg 105- (2) INFORMATION FOR SEQ ID NO:20:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 403 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA to mRNA- (vi) ORIGINAL SOURCE: (B) STRAIN: HYBRIDOMA K - #M-641- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide (B) LOCATION: 14..43 (C) IDENTIFICATION METHOD: BY SIMILA - #RITY WITH KNOWN SEQUENCE OR TO AN#CONSENSUS ESTABLISHED- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:20:- AATTCGGCAC GAG CTT GTC CTT GTT TTC AAA GGT GT - #T CAG TGT GAA GTG 49#Leu Val Phe Lys Gly Val Gln Cys Glu Val# 1- ACG CTG GTG GAG TCT GGG GGA GAC TTT GTG AA - #A CCT GGA GGG TCC CTG 97Thr Leu Val Glu Ser Gly Gly Asp Phe Val Ly - #s Pro Gly Gly Ser Leu# 15- AAA GTC TCC TGT GCA GCC TCT GGA TTC GCT TT - #C AGT CAT TAT GCC ATG 145Lys Val Ser Cys Ala Ala Ser Gly Phe Ala Ph - #e Ser His Tyr Ala Met# 30- TCT TGG GTT CGC CAG ACT CCG GCG AAG AGG CT - #G GAA TGG GTC GCA TAT 193Ser Trp Val Arg Gln Thr Pro Ala Lys Arg Le - #u Glu Trp Val Ala Tyr# 50- ATT AGT AGT GGT GGT AGT GGC ACC TAC TAT TC - #A GAC AGT GTA AAG GGC 241Ile Ser Ser Gly Gly Ser Gly Thr Tyr Tyr Se - #r Asp Ser Val Lys Gly# 65- CGA TTC ACC ATT TCC AGA GAC AAT GCC AAG AA - #C ACC CTG TAC CTG CAA 289Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys As - #n Thr Leu Tyr Leu Gln# 80- ATG CGC AGT CTG AGG TCT GAG GAC TCG GCC AT - #G TAT TTC TGT ACA AGA 337Met Arg Ser Leu Arg Ser Glu Asp Ser Ala Me - #t Tyr Phe Cys Thr Arg# 95- GTT AAA CTG GGA ACC TAC TAC TTT GAC TCC TG - #G GGC CAA GGC ACC ACT 385Val Lys Leu Gly Thr Tyr Tyr Phe Asp Ser Tr - #p Gly Gln Gly Thr Thr# 110# 403 CA GCTLeu Thr Val Ser Ser Ala115 1 - #20- (2) INFORMATION FOR SEQ ID NO:21:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 35 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:21:# 35 TTT GGG CTC AGC TGG CTT TTT Met Glu Phe Gly Leu S - #er Trp Leu Phe# 5 1- (2) INFORMATION FOR SEQ ID NO:22:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 43 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:22:- CAA GGT ACC ACG TTA ACT GTC TCC TCA GCC TC - #C ACC AAG GGC# 42Gln Gly Thr Thr Leu Thr Val Ser Ser Ala Se - #r Thr Lys Gly# 10# 43- (2) INFORMATION FOR SEQ ID NO:23:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 80 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:23:- GGCCGCACCA TGGGATGGAG CTGGATCTTT CTCTTCCTCC TGTCAGGAAC TG - #CTGGTGTC 60# 80 TGCA- (2) INFORMATION FOR SEQ ID NO:24:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 59 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:24:- GGAGAGCGGT CCAGGTCTTG TGAGGCCTAG CCAGACCCTG AGCCTGACCT GC - #ACCGTGT 59- (2) INFORMATION FOR SEQ ID NO:25:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 60 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:25:- CCGGATTCAC CTTCAGCGAC TACAACATGG ACTGGGTGAG ACAGCCACCT GG - #ACGAGGTC 60- (2) INFORMATION FOR SEQ ID NO:26:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 81 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:26:- TCGAGTGGAT TGGATATATT TATCCTAACA ATGGTGGTAC TGGCTACAAC CA - #GAAGTTCA 60#81 GCTG G- (2) INFORMATION FOR SEQ ID NO:27:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 61 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:27:- TCGACACCAG CAAGAACCAG TTCAGCCTGA GACTCAGCAG CGTGACAGCC GC - #CGACACCG 60# 61- (2) INFORMATION FOR SEQ ID NO:28:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 66 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:28:- GGTCTATTAT TGTGCGCGCT ACGGTCATTA CTACGGCTAC ATGTTTGCTT AC - #TGGGGTCA 60# 66- (2) INFORMATION FOR SEQ ID NO:29:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 35 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:29:# 35 TCAG CCTCCACCAA GGGCC- (2) INFORMATION FOR SEQ ID NO:30:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 77 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:30:- AATTCACCAT GCATTTTCAA GTGCAGATTT TCAGCTTCCT GCTAATCAGT GC - #CTCAGTCA 60# 77 T- (2) INFORMATION FOR SEQ ID NO:31:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 62 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:31:- ATCCAGCTGA CCCAGAGCCC AAGCAGCCTG AGCGCTAGCG TGGGTGACAG AG - #TGACCATG 60# 62- (2) INFORMATION FOR SEQ ID NO:32:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 65 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:32:- GTGCAGTGCC AGCTCAAGTG TAAGTTACAT GCACTGGTAT CAGCAGAAGC CA - #GGTAAGGC 60# 65- (2) INFORMATION FOR SEQ ID NO:33:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 45 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:33:#45 CACA TCCAACCTGG CTTCTGGTGT GCCAT- (2) INFORMATION FOR SEQ ID NO:34:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 76 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:34:- CTAGATTCAG CGGTAGCGGT AGCGGTACAG ACTTCACCTT CACCATCAGC AG - #CCTCCAGC 60# 76- (2) INFORMATION FOR SEQ ID NO:35:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 84 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear#synthetic DNAECULE TYPE: other nucleic acid,- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:35:- GTACTACTGC CAGCAAAGGA GTAGTTACCC GTACACGTTC GGCGGGGGGA CC - #AAGGTGGA 60# 84GCTG CACC- (2) INFORMATION FOR SEQ ID NO:36:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 442 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:36:- GGCCGCACC ATG GGA TGG AGC TGG ATC TTT CTC TTC - # CTC CTG TCA GGA 48#Ile Phe Leu Phe Leu Leu Ser Gly10- ACT GCT GGT GTC CTC TCT CAG GTC CAA CTG CA - #G GAG AGC GGT CCA GGT 96Thr Ala Gly Val Leu Ser Gln Val Gln Leu Gl - #n Glu Ser Gly Pro Gly# 10- CTT GTG AGG CCT AGC CAG ACC CTG AGC CTG AC - #C TGC ACC GTG TCC GGA 144Leu Val Arg Pro Ser Gln Thr Leu Ser Leu Th - #r Cys Thr Val Ser Gly# 25- TTC ACC TTC AGC GAC TAC AAC ATG GAC TGG GT - #G AGA CAG CCA CCT GGA 192Phe Thr Phe Ser Asp Tyr Asn Met Asp Trp Va - #l Arg Gln Pro Pro Gly# 40- CGA GGT CTC GAG TGG ATT GGA TAT ATT TAT CC - #T AAC AAT GGT GGT ACT 240Arg Gly Leu Glu Trp Ile Gly Tyr Ile Tyr Pr - #o Asn Asn Gly Gly Thr# 55- GGC TAC AAC CAG AAG TTC AAG AGC AGA GTG AC - #A ATG CTG GTC GAC ACC 288Gly Tyr Asn Gln Lys Phe Lys Ser Arg Val Th - #r Met Leu Val Asp Thr# 70- AGC AAG AAC CAG TTC AGC CTG AGA CTC AGC AG - #C GTG ACA GCC GCC GAC 336Ser Lys Asn Gln Phe Ser Leu Arg Leu Ser Se - #r Val Thr Ala Ala Asp# 90- ACC GCG GTC TAT TAT TGT GCG CGC TAC GGT CA - #T TAC TAC GGC TAC ATG 384Thr Ala Val Tyr Tyr Cys Ala Arg Tyr Gly Hi - #s Tyr Tyr Gly Tyr Met# 105- TTT GCT TAC TGG GGT CAA GGT ACC ACC GTC AC - #A GTC TCC TCA GCC TCC 432Phe Ala Tyr Trp Gly Gln Gly Thr Thr Val Th - #r Val Ser Ser Ala Ser# 120# 442Thr Lys Gly 125- (2) INFORMATION FOR SEQ ID NO:37:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 409 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:37:#TTC CTG CTA ATC AGT 50TG CAG ATT TTC AGC Met His Phe Gln Val G - #ln Ile Phe Ser Phe Leu Leu Ile Ser10- GCC TCA GTC ATA ATG TCC AGA GGA GAT ATC CA - #G CTG ACC CAG AGC CCA 98Ala Ser Val Ile Met Ser Arg Gly Asp Ile Gl - #n Leu Thr Gln Ser Pro# 5 1- AGC AGC CTG AGC GCT AGC GTG GGT GAC AGA GT - #G ACC ATC ACG TGC AGT 146Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Va - #l Thr Ile Thr Cys Ser# 20- GCC AGC TCA AGT GTA AGT TAC ATG CAC TGG TA - #T CAG CAG AAG CCA GGT 194Ala Ser Ser Ser Val Ser Tyr Met His Trp Ty - #r Gln Gln Lys Pro Gly# 40- AAG GCT CCA AAG CTT CTG ATC TAC AGC ACA TC - #C AAC CTG GCT TCT GGT 242Lys Ala Pro Lys Leu Leu Ile Tyr Ser Thr Se - #r Asn Leu Ala Ser Gly# 55- GTG CCA TCT AGA TTC AGC GGT AGC GGT AGC GG - #T ACA GAC TTC ACC TTC 290Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gl - #y Thr Asp Phe Thr Phe# 70- ACC ATC AGC AGC CTC CAG CCA GAG GAC ATC GC - #T ACG TAC TAC TGC CAG 338Thr Ile Ser Ser Leu Gln Pro Glu Asp Ile Al - #a Thr Tyr Tyr Cys Gln# 85- CAA AGG AGT AGT TAC CCG TAC ACG TTC GGC GG - #G GGG ACC AAG GTG GAA 386Gln Arg Ser Ser Tyr Pro Tyr Thr Phe Gly Gl - #y Gly Thr Lys Val Glu# 100# 409TG GCT GCA CCIle Lys Arg Thr Val Ala Ala105 1 - #10- (2) INFORMATION FOR SEQ ID NO:38:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:38:# 32 AGGA GCAGGTGAAT TC- (2) INFORMATION FOR SEQ ID NO:39:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 40 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:39:# 40 TCCT CAGTTAACAC TGAGTGGTAC- (2) INFORMATION FOR SEQ ID NO:40:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 21 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:40:#21 GCAC C- (2) INFORMATION FOR SEQ ID NO:41:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 17 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:41:# 17 G- (2) INFORMATION FOR SEQ ID NO:42:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 26 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:42:# 26 CCGC GGCCGC- (2) INFORMATION FOR SEQ ID NO:43:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 34 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:43:# 34 CCAC TAGTCGCGAG GTAC- (2) INFORMATION FOR SEQ ID NO:44:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 20 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:44:# 20 CCCG- (2) INFORMATION FOR SEQ ID NO:45:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 20 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:45:# 20 CCAC- (2) INFORMATION FOR SEQ ID NO:46:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:46:# 36 GGTT CGATAAATCG ATACCG- (2) INFORMATION FOR SEQ ID NO:47:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 40 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:47:# 40 AACC GTACGAAGAA TTCATGAGCT- (2) INFORMATION FOR SEQ ID NO:48:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 35 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:48:# 35 ACCA AGCTGGAAAT AAAAC- (2) INFORMATION FOR SEQ ID NO:49:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 35 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:49:# 35 GCTT GGTCCCCCCT CCGAA- (2) INFORMATION FOR SEQ ID NO:50:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 61 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:50:- TCGACACCAG CAAGAACACA GCCTACCTGA GACTCAGCAG CGTGACAGCC GC - #CGACACCG 60# 61- (2) INFORMATION FOR SEQ ID NO:51:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 59 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:51:- CCGGATACAC ATTCACTGAC TACAACATGG ACTGGGTGAG ACAGAGCCAT GA - #CGAGGTC 59- (2) INFORMATION FOR SEQ ID NO:52:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 442 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide19..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 31..35 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 50..66 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 99..109 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:52:- GGCCGCACC ATG GGA TGG AGC TGG ATC TTT CTC TTC - # CTC CTG TCA GGA 48#Ile Phe Leu Phe Leu Leu Ser Gly10- ACT GCT GGT GTC CTC TCT CAG GTC CAA CTG CA - #G GAG AGC GGT CCA GGT 96Thr Ala Gly Val Leu Ser Gln Val Gln Leu Gl - #n Glu Ser Gly Pro Gly# 10- CTT GTG AGG CCT AGC CAG ACC CTG AGC CTG AC - #C TGC ACC GTG TCC GGA 144Leu Val Arg Pro Ser Gln Thr Leu Ser Leu Th - #r Cys Thr Val Ser Gly# 25- TTC ACC TTC AGC GAC TAC AAC ATG GAC TGG GT - #G AGA CAG CCA CCT GGA 192Phe Thr Phe Ser Asp Tyr Asn Met Asp Trp Va - #l Arg Gln Pro Pro Gly# 40- CGA GGT CTC GAG TGG ATT GGA TAT ATT TAT CC - #T AAC AAT GGT GGT ACT 240Arg Gly Leu Glu Trp Ile Gly Tyr Ile Tyr Pr - #o Asn Asn Gly Gly Thr# 55- GGC TAC AAC CAG AAG TTC AAG AGC AGA GTG AC - #A ATG CTG GTC GAC ACC 288Gly Tyr Asn Gln Lys Phe Lys Ser Arg Val Th - #r Met Leu Val Asp Thr# 70- AGC AAG AAC ACA GCC TAC CTG AGA CTC AGC AG - #C GTG ACA GCC GCC GAC 336Ser Lys Asn Thr Ala Tyr Leu Arg Leu Ser Se - #r Val Thr Ala Ala Asp# 90- ACC GCG GTC TAT TAT TGT GCA ACC TAC GGT CA - #T TAC TAC GGC TAC ATG 384Thr Ala Val Tyr Tyr Cys Ala Thr Tyr Gly Hi - #s Tyr Tyr Gly Tyr Met# 105- TTT GCT TAC TGG GGT CAA GGT ACC ACC GTC AC - #A GTC TCC TCA GCC TCC 432Phe Ala Tyr Trp Gly Gln Gly Thr Thr Val Th - #r Val Ser Ser Ala Ser# 120# 442Thr Lys Gly 125- (2) INFORMATION FOR SEQ ID NO:53:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 442 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide19..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 31..35 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 50..66 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 99..109 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:53:- GGCCGCACC ATG GGA TGG AGC TGG ATC TTT CTC TTC - # CTC CTG TCA GGA 48#Ile Phe Leu Phe Leu Leu Ser Gly10- ACT GCT GGT GTC CTC TCT CAG GTC CAA CTG CA - #G GAG AGC GGT CCA GGT 96Thr Ala Gly Val Leu Ser Gln Val Gln Leu Gl - #n Glu Ser Gly Pro Gly# 10- CTT GTG AGG CCT AGC CAG ACC CTG AGC CTG AC - #C TGC ACC GTG TCC GGA 144Leu Val Arg Pro Ser Gln Thr Leu Ser Leu Th - #r Cys Thr Val Ser Gly# 25- TAC ACA TTC ACT GAC TAC AAC ATG GAC TGG GT - #G AGA CAG AGC CAT GGA 192Tyr Thr Phe Thr Asp Tyr Asn Met Asp Trp Va - #l Arg Gln Ser His Gly# 40- CGA GGT CTC GAG TGG ATT GGA TAT ATT TAT CC - #T AAC AAT GGT GGT ACT 240Arg Gly Leu Glu Trp Ile Gly Tyr Ile Tyr Pr - #o Asn Asn Gly Gly Thr# 55- GGC TAC AAC CAG AAG TTC AAG AGC AGA GTG AC - #A ATG CTG GTC GAC ACC 288Gly Tyr Asn Gln Lys Phe Lys Ser Arg Val Th - #r Met Leu Val Asp Thr# 70- AGC AAG AAC CAG TTC AGC CTG AGA CTC AGC AG - #C GTG ACA GCC GCC GAC 336Ser Lys Asn Gln Phe Ser Leu Arg Leu Ser Se - #r Val Thr Ala Ala Asp# 90- ACC GCG GTC TAT TAT TGT GCA ACC TAC GGT CA - #T TAC TAC GGC TAC ATG 384Thr Ala Val Tyr Tyr Cys Ala Thr Tyr Gly Hi - #s Tyr Tyr Gly Tyr Met# 105- TTT GCT TAC TGG GGT CAA GGT ACC ACC GTC AC - #A GTC TCC TCA GCC TCC 432Phe Ala Tyr Trp Gly Gln Gly Thr Thr Val Th - #r Val Ser Ser Ala Ser# 120# 442Thr Lys Gly 125- (2) INFORMATION FOR SEQ ID NO:54:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 100 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:54:- CAGGAAACAG CTATGACGCG GCCGCCACCA TGGGATGGAG CTGGATCTTT CT - #CTTCCTCC 60# 100 TGTC CTCTCTGAGG TGCAGCTGGT- (2) INFORMATION FOR SEQ ID NO:55:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 100 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:55:- AGTCAGTGAA GGTGTATCCG GAAGCCTTGC AGGAGACCTT CACTGAGGCC CC - #AGGCTTCT 60# 100 CTGC ACCAGCTGCA CCTCAGAGAG- (2) INFORMATION FOR SEQ ID NO:56:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 100 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:56:- CGGATACACC TTCACTGACT ACAACATGGA CTGGGTGCGA CAGGCCCCTG GA - #CAAGGGCT 60# 100 ATTT ATCCTAACAA TGGTGGTACT- (2) INFORMATION FOR SEQ ID NO:57:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 94 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:57:- AGCTCCATGT AGGCTGTGCT CGTGGATGTG TCTACGGTAA TGGTGACCTT GC - #TCTTGAAC 60# 94 TACC ACCATTGTTA GGAT- (2) INFORMATION FOR SEQ ID NO:58:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 96 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:58:- AGCACAGCCT ACATGGAGCT GCACAGCCTG AGATCTGAGG ACACGGCCGT GT - #ATTACTGT 60# 96 ACTA CGGCTACATG TTTGCT- (2) INFORMATION FOR SEQ ID NO:59:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 90 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:59:- GTTTTCCCAG TCACGACGGG CCCTTGGTGG AGGCTGAGGA GACGGTGACC AG - #GGTTCCCT 60# 90 CATG TAGCCGTAGT- (2) INFORMATION FOR SEQ ID NO:60:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 432 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide19..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 31..35 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#an established consensu#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 50..66 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 99..109 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:60:- ATG GGA TGG AGC TGG ATC TTT CTC TTC CTC CT - #G TCA GGA ACT GCA GGT 48Met Gly Trp Ser Trp Ile Phe Leu Phe Leu Le - #u Ser Gly Thr Ala Gly5- GTC CTC TCT GAG GTG CAG CTG GTG CAG TCT GG - #A GCA GAG GTG AAG AAG 96Val Leu Ser Glu Val Gln Leu Val Gln Ser Gl - #y Ala Glu Val Lys Lys# 10- CCT GGG GCC TCA GTG AAG GTC TCC TGC AAG GC - #T TCC GGA TAC ACC TTC 144Pro Gly Ala Ser Val Lys Val Ser Cys Lys Al - #a Ser Gly Tyr Thr Phe# 25- ACT GAC TAC AAC ATG GAC TGG GTG CGA CAG GC - #C CCT GGA CAA GGG CTC 192Thr Asp Tyr Asn Met Asp Trp Val Arg Gln Al - #a Pro Gly Gln Gly Leu# 45- GAG TGG ATG GGA TAT ATT TAT CCT AAC AAT GG - #T GGT ACT GGC TAC AAC 240Glu Trp Met Gly Tyr Ile Tyr Pro Asn Asn Gl - #y Gly Thr Gly Tyr Asn# 60- CAG AAG TTC AAG AGC AAG GTC ACC ATT ACC GT - #A GAC ACA TCC ACG AGC 288Gln Lys Phe Lys Ser Lys Val Thr Ile Thr Va - #l Asp Thr Ser Thr Ser# 75- ACA GCC TAC ATG GAG CTG CAC AGC CTG AGA TC - #T GAG GAC ACG GCC GTG 336Thr Ala Tyr Met Glu Leu His Ser Leu Arg Se - #r Glu Asp Thr Ala Val# 90- TAT TAC TGT GCG ACC TAC GGT CAT TAC TAC GG - #C TAC ATG TTT GCT TAC 384Tyr Tyr Cys Ala Thr Tyr Gly His Tyr Tyr Gl - #y Tyr Met Phe Ala Tyr# 105- TGG GGC CAG GGA ACC CTG GTC ACC GTC TCC TC - #A GCC TCC ACC AAG GGC 432Trp Gly Gln Gly Thr Leu Val Thr Val Ser Se - #r Ala Ser Thr Lys Gly110 1 - #15 1 - #20 1 -#25- (2) INFORMATION FOR SEQ ID NO:61:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 68 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:61:- GTACTACTGC CAGCAAAGGA GTAGTTACCC GTACACGTTC GGCGGGGGGA CC - #AAGGTGGA 60# 68- (2) INFORMATION FOR SEQ ID NO:62:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 25 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:62:# 25 TAGC GCTCA- (2) INFORMATION FOR SEQ ID NO:63:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 25 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:63:# 25 TGAC AGAGT- (2) INFORMATION FOR SEQ ID NO:64:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 390 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:64:- ATG CAT TTT CAA GTG CAG ATT TTC AGC TTC CT - #G CTA ATC AGT GCC TCA 48Met His Phe Gln Val Gln Ile Phe Ser Phe Le - #u Leu Ile Ser Ala Ser10- GTC ATA ATG TCC AGA GGA GAT ATC CAG CTG AC - #C CAG AGC CCA AGC AGC 96Val Ile Met Ser Arg Gly Asp Ile Gln Leu Th - #r Gln Ser Pro Ser Ser# 10- CTG AGC GCT AGC CCA GGT GAC AGA GTG ACC AT - #C ACG TGC AGT GCC AGC 144Leu Ser Ala Ser Pro Gly Asp Arg Val Thr Il - #e Thr Cys Ser Ala Ser# 25- TCA AGT GTA AGT TAC ATG CAC TGG TAT CAG CA - #G AAG CCA GGT AAG GCT 192Ser Ser Val Ser Tyr Met His Trp Tyr Gln Gl - #n Lys Pro Gly Lys Ala# 40- CCA AAG CTT CTG ATC TAC AGC ACA TCC AAC CT - #G GCT TCT GGT GTG CCA 240Pro Lys Leu Leu Ile Tyr Ser Thr Ser Asn Le - #u Ala Ser Gly Val Pro# 55- TCT AGA TTC AGC GGT AGC GGT AGC GGT ACA GA - #C TTC ACC TTC ACC ATC 288Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr As - #p Phe Thr Phe Thr Ile# 70- AGC AGC CTC CAG CCA GAG GAC ATC GCT ACG TA - #C TAC TGC CAG CAA AGG 336Ser Ser Leu Gln Pro Glu Asp Ile Ala Thr Ty - #r Tyr Cys Gln Gln Arg# 90- AGT AGT TAC CCG TAC ACG TTC GGC GGG GGG AC - #C AAG GTG GAA ATC AAA 384Ser Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Th - #r Lys Val Glu Ile Lys# 105# 390Arg Thr- (2) INFORMATION FOR SEQ ID NO:65:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 25 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:65:# 25 GCTT TGGAG- (2) INFORMATION FOR SEQ ID NO:66:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 25 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:66:# 25 CTAC AGCAC- (2) INFORMATION FOR SEQ ID NO:67:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 390 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:67:- ATG CAT TTT CAA GTG CAG ATT TTC AGC TTC CT - #G CTA ATC AGT GCC TCA 48Met His Phe Gln Val Gln Ile Phe Ser Phe Le - #u Leu Ile Ser Ala Ser10- GTC ATA ATG TCC AGA GGA GAT ATC CAG CTG AC - #C CAG AGC CCA AGC AGC 96Val Ile Met Ser Arg Gly Asp Ile Gln Leu Th - #r Gln Ser Pro Ser Ser# 10- CTG AGC GCT AGC GTG GGT GAC AGA GTG ACC AT - #C ACG TGC AGT GCC AGC 144Leu Ser Ala Ser Val Gly Asp Arg Val Thr Il - #e Thr Cys Ser Ala Ser# 25- TCA AGT GTA AGT TAC ATG CAC TGG TAT CAG CA - #G AAG CCA GGT AAG GCT 192Ser Ser Val Ser Tyr Met His Trp Tyr Gln Gl - #n Lys Pro Gly Lys Ala# 40- CCA AAG CTT TGG ATC TAC AGC ACA TCC AAC CT - #G GCT TCT GGT GTG CCA 240Pro Lys Leu Trp Ile Tyr Ser Thr Ser Asn Le - #u Ala Ser Gly Val Pro# 55- TCT AGA TTC AGC GGT AGC GGT AGC GGT ACA GA - #C TTC ACC TTC ACC ATC 288Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr As - #p Phe Thr Phe Thr Ile# 70- AGC AGC CTC CAG CCA GAG GAC ATC GCT ACG TA - #C TAC TGC CAG CAA AGG 336Ser Ser Leu Gln Pro Glu Asp Ile Ala Thr Ty - #r Tyr Cys Gln Gln Arg# 90- AGT AGT TAC CCG TAC ACG TTC GGC GGG GGG AC - #C AAG GTG GAA ATC AAA 384Ser Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Th - #r Lys Val Glu Ile Lys# 105# 390Arg Thr- (2) INFORMATION FOR SEQ ID NO:68:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 25 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:68:# 25 AGCC TGGAG- (2) INFORMATION FOR SEQ ID NO:69:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 25 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:69:# 25 CTGC TACGT- (2) INFORMATION FOR SEQ ID NO:70:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 390 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:70:- ATG CAT TTT CAA GTG CAG ATT TTC AGC TTC CT - #G CTA ATC AGT GCC TCA 48Met His Phe Gln Val Gln Ile Phe Ser Phe Le - #u Leu Ile Ser Ala Ser10- GTC ATA ATG TCC AGA GGA GAT ATC CAG CTG AC - #C CAG AGC CCA AGC AGC 96Val Ile Met Ser Arg Gly Asp Ile Gln Leu Th - #r Gln Ser Pro Ser Ser# 10- CTG AGC GCT AGC GTG GGT GAC AGA GTG ACC AT - #C ACG TGC AGT GCC AGC 144Leu Ser Ala Ser Val Gly Asp Arg Val Thr Il - #e Thr Cys Ser Ala Ser# 25- TCA AGT GTA AGT TAC ATG CAC TGG TAT CAG CA - #G AAG CCA GGT AAG GCT 192Ser Ser Val Ser Tyr Met His Trp Tyr Gln Gl - #n Lys Pro Gly Lys Ala# 40- CCA AAG CTT CTG ATC TAC AGC ACA TCC AAC CT - #G GCT TCT GGT GTG CCA 240Pro Lys Leu Leu Ile Tyr Ser Thr Ser Asn Le - #u Ala Ser Gly Val Pro# 55- TCT AGA TTC AGC GGT AGC GGT AGC GGT ACA GA - #C TTC ACC TTC ACC ATC 288Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr As - #p Phe Thr Phe Thr Ile# 70- AGC AGC CTC CAG GCT GAA GAT GCT GCT ACG TA - #C TAC TGC CAG CAA AGG 336Ser Ser Leu Gln Ala Glu Asp Ala Ala Thr Ty - #r Tyr Cys Gln Gln Arg# 90- AGT AGT TAC CCG TAC ACG TTC GGC GGG GGG AC - #C AAG GTG GAA ATC AAA 384Ser Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Th - #r Lys Val Glu Ile Lys# 105# 390Arg Thr- (2) INFORMATION FOR SEQ ID NO:71:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 25 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:71:# 25 ATGT ACCGC- (2) INFORMATION FOR SEQ ID NO:72:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 25 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:72:# 25 TTTC ACCAT- (2) INFORMATION FOR SEQ ID NO:73:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 390 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:73:- ATG CAT TTT CAA GTG CAG ATT TTC AGC TTC CT - #G CTA ATC AGT GCC TCA 48Met His Phe Gln Val Gln Ile Phe Ser Phe Le - #u Leu Ile Ser Ala Ser10- GTC ATA ATG TCC AGA GGA GAT ATC CAG CTG AC - #C CAG AGC CCA AGC AGC 96Val Ile Met Ser Arg Gly Asp Ile Gln Leu Th - #r Gln Ser Pro Ser Ser# 10- CTG AGC GCT AGC CCA GGT GAC AGA GTG ACC AT - #C ACG TGC AGT GCC AGC 144Leu Ser Ala Ser Pro Gly Asp Arg Val Thr Il - #e Thr Cys Ser Ala Ser# 25- TCA AGT GTA AGT TAC ATG CAC TGG TAT CAG CA - #G AAG CCA GGT AAG GCT 192Ser Ser Val Ser Tyr Met His Trp Tyr Gln Gl - #n Lys Pro Gly Lys Ala# 40- CCA AAG CTT TGG ATC TAC AGC ACA TCC AAC CT - #G GCT TCT GGT GTG CCA 240Pro Lys Leu Trp Ile Tyr Ser Thr Ser Asn Le - #u Ala Ser Gly Val Pro# 55- TCT AGA TTC AGC GGT AGC GGT AGC GGT ACA TC - #T TAC TCT TTC ACC ATC 288Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Se - #r Tyr Ser Phe Thr Ile# 70- AGC AGC CTC CAG CCA GAG GAC ATC GCT ACG TA - #C TAC TGC CAG CAA AGG 336Ser Ser Leu Gln Pro Glu Asp Ile Ala Thr Ty - #r Tyr Cys Gln Gln Arg# 90- AGT AGT TAC CCG TAC ACG TTC GGC GGG GGG AC - #C AAG GTG GAA ATC AAA 384Ser Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Th - #r Lys Val Glu Ile Lys# 105# 390Arg Thr- (2) INFORMATION FOR SEQ ID NO:74:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 40 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:74:# 40 TGAT GGTGAAAGAG TAAGATGTAC- (2) INFORMATION FOR SEQ ID NO:75:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 40 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:75:# 40 CACC ATCAGCCGAA TGGAGCCAGA- (2) INFORMATION FOR SEQ ID NO:76:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 390 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:76:- ATG CAT TTT CAA GTG CAG ATT TTC AGC TTC CT - #G CTA ATC AGT GCC TCA 48Met His Phe Gln Val Gln Ile Phe Ser Phe Le - #u Leu Ile Ser Ala Ser10- GTC ATA ATG TCC AGA GGA GAT ATC CAG CTG AC - #C CAG AGC CCA AGC AGC 96Val Ile Met Ser Arg Gly Asp Ile Gln Leu Th - #r Gln Ser Pro Ser Ser# 10- CTG AGC GCT AGC CCA GGT GAC AGA GTG ACC AT - #C ACG TGC AGT GCC AGC 144Leu Ser Ala Ser Pro Gly Asp Arg Val Thr Il - #e Thr Cys Ser Ala Ser# 25- TCA AGT GTA AGT TAC ATG CAC TGG TAT CAG CA - #G AAG CCA GGT AAG GCT 192Ser Ser Val Ser Tyr Met His Trp Tyr Gln Gl - #n Lys Pro Gly Lys Ala# 40- CCA AAG CTT TGG ATC TAC AGC ACA TCC AAC CT - #G GCT TCT GGT GTG CCA 240Pro Lys Leu Trp Ile Tyr Ser Thr Ser Asn Le - #u Ala Ser Gly Val Pro# 55- TCT AGA TTC AGC GGT AGC GGT AGC GGT ACA TC - #T TAC TCT TTC ACC ATC 288Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Se - #r Tyr Ser Phe Thr Ile# 70- AGC CGA ATG GAG CCA GAG GAC ATC GCT ACG TA - #C TAC TGC CAG CAA AGG 336Ser Arg Met Glu Pro Glu Asp Ile Ala Thr Ty - #r Tyr Cys Gln Gln Arg# 90- AGT AGT TAC CCG TAC ACG TTC GGC GGG GGG AC - #C AAG GTG GAA ATC AAA 384Ser Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Th - #r Lys Val Glu Ile Lys# 105# 390Arg Thr- (2) INFORMATION FOR SEQ ID NO:77:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 20 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:77:# 20 GCAT- (2) INFORMATION FOR SEQ ID NO:78:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 20 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:78:# 20 AGAA- (2) INFORMATION FOR SEQ ID NO:79:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 390 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:79:- ATG CAT TTT CAA GTG CAG ATT TTC AGC TTC CT - #G CTA ATC AGT GCC TCA 48Met His Phe Gln Val Gln Ile Phe Ser Phe Le - #u Leu Ile Ser Ala Ser10- GTC ATA ATG TCC AGA GGA GAT ATC CAG CTG AC - #C CAG AGC CCA AGC AGC 96Val Ile Met Ser Arg Gly Asp Ile Gln Leu Th - #r Gln Ser Pro Ser Ser# 10- CTG AGC GCT AGC CCA GGT GAC AGA GTG ACC AT - #C ACG TGC AGT GCC AGC 144Leu Ser Ala Ser Pro Gly Asp Arg Val Thr Il - #e Thr Cys Ser Ala Ser# 25- TCA AGT GTA AGT TAC ATG CAC TGG TTC CAG CA - #G AAG CCA GGT AAG GCT 192Ser Ser Val Ser Tyr Met His Trp Phe Gln Gl - #n Lys Pro Gly Lys Ala# 40- CCA AAG CTT TGG ATC TAC AGC ACA TCC AAC CT - #G GCT TCT GGT GTG CCA 240Pro Lys Leu Trp Ile Tyr Ser Thr Ser Asn Le - #u Ala Ser Gly Val Pro# 55- TCT AGA TTC AGC GGT AGC GGT AGC GGT ACA TC - #T TAC TCT TTC ACC ATC 288Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Se - #r Tyr Ser Phe Thr Ile# 70- AGC AGC CTC CAG CCA GAG GAC ATC GCT ACG TA - #C TAC TGC CAG CAA AGG 336Ser Ser Leu Gln Pro Glu Asp Ile Ala Thr Ty - #r Tyr Cys Gln Gln Arg# 90- AGT AGT TAC CCG TAC ACG TTC GGC GGG GGG AC - #C AAG GTG GAA ATC AAA 384Ser Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Th - #r Lys Val Glu Ile Lys# 105# 390Arg Thr- (2) INFORMATION FOR SEQ ID NO:80:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 25 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:80:# 25 TGAG AGAGT- (2) INFORMATION FOR SEQ ID NO:81:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 25 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:81:# 25 CCGA CTCCA- (2) INFORMATION FOR SEQ ID NO:82:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 390 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:82:- ATG CAT TTT CAA GTG CAG ATT TTC AGC TTC CT - #G CTA ATC AGT GCC TCA 48Met His Phe Gln Val Gln Ile Phe Ser Phe Le - #u Leu Ile Ser Ala Ser10- GTC ATA ATG TCC AGA GGA GAT ATC CAG CTG AC - #C CAG AGC CCA AGC AGC 96Val Ile Met Ser Arg Gly Asp Ile Gln Leu Th - #r Gln Ser Pro Ser Ser# 10- CTG AGC GCT AGC CCA GGT GAC AGA GTG ACC AT - #C ACG TGC AGT GCC AGC 144Leu Ser Ala Ser Pro Gly Asp Arg Val Thr Il - #e Thr Cys Ser Ala Ser# 25- TCA AGT GTA AGT TAC ATG CAC TGG TAT CAG CA - #G AAG CCA GGT AAG GCT 192Ser Ser Val Ser Tyr Met His Trp Tyr Gln Gl - #n Lys Pro Gly Lys Ala# 40- CCA AAG CTT TGG ATC TAC AGC ACA TCC AAC CT - #G GCT TCT GGT GTG CCA 240Pro Lys Leu Trp Ile Tyr Ser Thr Ser Asn Le - #u Ala Ser Gly Val Pro# 55- TCT AGA TTC AGC GGT AGC GGT AGC GGT ACA TC - #T TAC TCT CTC ACC ATC 288Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Se - #r Tyr Ser Leu Thr Ile# 70- AGC CGA CTC CAG CCA GAG GAC ATC GCT ACG TA - #C TAC TGC CAG CAA AGG 336Ser Arg Leu Gln Pro Glu Asp Ile Ala Thr Ty - #r Tyr Cys Gln Gln Arg# 90- AGT AGT TAC CCG TAC ACG TTC GGC GGG GGG AC - #C AAG GTG GAA ATC AAA 384Ser Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Th - #r Lys Val Glu Ile Lys# 105# 390Arg Thr- (2) INFORMATION FOR SEQ ID NO:83:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 390 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:83:- ATG CAT TTT CAA GTG CAG ATT TTC AGC TTC CT - #G CTA ATC AGT GCC TCA 48Met His Phe Gln Val Gln Ile Phe Ser Phe Le - #u Leu Ile Ser Ala Ser10- GTC ATA ATG TCC AGA GGA GAT ATC CAG CTG AC - #C CAG AGC CCA AGC AGC 96Val Ile Met Ser Arg Gly Asp Ile Gln Leu Th - #r Gln Ser Pro Ser Ser# 10- CTG AGC GCT AGC CCA GGT GAC AGA GTG ACC AT - #C ACG TGC AGT GCC AGC 144Leu Ser Ala Ser Pro Gly Asp Arg Val Thr Il - #e Thr Cys Ser Ala Ser# 25- TCA AGT GTA AGT TAC ATG CAC TGG TTC CAG CA - #G AAG CCA GGT AAG GCT 192Ser Ser Val Ser Tyr Met His Trp Phe Gln Gl - #n Lys Pro Gly Lys Ala# 40- CCA AAG CTT TGG ATC TAC AGC ACA TCC AAC CT - #G GCT TCT GGT GTG CCA 240Pro Lys Leu Trp Ile Tyr Ser Thr Ser Asn Le - #u Ala Ser Gly Val Pro# 55- TCT AGA TTC AGC GGT AGC GGT AGC GGT ACA TC - #T TAC TCT CTC ACC ATC 288Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Se - #r Tyr Ser Leu Thr Ile# 70- AGC CGA CTC CAG CCA GAG GAC ATC GCT ACG TA - #C TAC TGC CAG CAA AGG 336Ser Arg Leu Gln Pro Glu Asp Ile Ala Thr Ty - #r Tyr Cys Gln Gln Arg# 90- AGT AGT TAC CCG TAC ACG TTC GGC GGG GGG AC - #C AAG GTG GAA ATC AAA 384Ser Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Th - #r Lys Val Glu Ile Lys# 105# 390Arg Thr- (2) INFORMATION FOR SEQ ID NO:84:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 94 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:84:- CAGGAAACAG CTATGACGAA TTCCACCATG CATTTTCAAG TGCAGATTTT CA - #GCTTCCTG 60# 94 TCAT AATGTCCAGA GGAG- (2) INFORMATION FOR SEQ ID NO:85:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 88 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:85:- ACAAGTGATG GTGACTCTGT CTCCTGGAGA TGCAGACATG GAGGATGGAG AC - #TGGGTCAG 60# 88 GACA TTATGACT- (2) INFORMATION FOR SEQ ID NO:86:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 92 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:86:- ACAGAGTCAC CATCACTTGT AGTGCAAGTT CAAGTGTAAG TTACATGCAC TG - #GTTTCAGC 60# 92 ACCT AAGCTCTGGA TC- (2) INFORMATION FOR SEQ ID NO:87:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 87 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:87:- AAGATGTACC GCTACCGCTA CCGCTGAATC TAGATGGCAC ACCAGAAGCT AA - #ATTTGAAG 60# 87 CTTA GGTGATT- (2) INFORMATION FOR SEQ ID NO:88:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 89 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:88:- TAGCGGTAGC GGTACATCTT ACTCTCTCAC CATCAGCAGC ATGCAGCCTG AA - #GATTTTGC 60# 89 CAAA GGAGTAGTT- (2) INFORMATION FOR SEQ ID NO:89:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 84 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:89:- GTTTTCCCAG TCACGACCGT ACGTTTGATT TCCAGCTTGG TCCCCTGGCC GA - #ACGTGTAC 60# 84GCTG ACAG- (2) INFORMATION FOR SEQ ID NO:90:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 390 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (vi) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens and mouse- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR1"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR2"ER INFORMATION:- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # by similarity with knownsequence#established consensun#/product= "CDR3"ER INFORMATION:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:90:- ATG CAT TTT CAA GTG CAG ATT TTC AGC TTC CT - #G CTA ATC AGT GCC TCA 48Met His Phe Gln Val Gln Ile Phe Ser Phe Le - #u Leu Ile Ser Ala Ser10- GTC ATA ATG TCC AGA GGA GAC ATC CAG CTG AC - #C CAG TCT CCA TCC TCC 96Val Ile Met Ser Arg Gly Asp Ile Gln Leu Th - #r Gln Ser Pro Ser Ser# 10- ATG TCT GCA TCT CCA GGA GAC AGA GTC ACC AT - #C ACT TGT AGT GCA AGT 144Met Ser Ala Ser Pro Gly Asp Arg Val Thr Il - #e Thr Cys Ser Ala Ser# 25- TCA AGT GTA AGT TAC ATG CAC TGG TTT CAG CA - #G AAA CCA GGG AAA TCA 192Ser Ser Val Ser Tyr Met His Trp Phe Gln Gl - #n Lys Pro Gly Lys Ser# 40- CCT AAG CTC TGG ATC TAC TCA ACT TCA AAT TT - #A GCT TCT GGT GTG CCA 240Pro Lys Leu Trp Ile Tyr Ser Thr Ser Asn Le - #u Ala Ser Gly Val Pro# 55- TCT AGA TTC AGC GGT AGC GGT AGC GGT ACA TC - #T TAC TCT CTC ACC ATC 288Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Se - #r Tyr Ser Leu Thr Ile# 70- AGC AGC ATG CAG CCT GAA GAT TTT GCA ACT TA - #T TAC TGT CAG CAA AGG 336Ser Ser Met Gln Pro Glu Asp Phe Ala Thr Ty - #r Tyr Cys Gln Gln Arg# 90- AGT AGT TAC CCG TAC ACG TTC GGC CAG GGG AC - #C AAG CTG GAA ATC AAA 384Ser Ser Tyr Pro Tyr Thr Phe Gly Gln Gly Th - #r Lys Leu Glu Ile Lys# 105# 390Arg Thr- (2) INFORMATION FOR SEQ ID NO:91:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 139 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide19..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: BY SIMILA - #RITY WITH KNOWN SEQUENCE OR TO AN#CONSENSUS ESTABLISHED- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 31..35 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 1"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 50..66 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 2"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 99..109 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 3"- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:91:#Met Gly Trp Ser Trp Ile Phe15- Leu Phe Leu Leu Ser Gly Thr Ala Gly Val Le - #u Ser Glu Val Gln Leu# 1- Gln Gln Ser Gly Pro Glu Leu Val Lys Pro Gl - #y Ala Ser Val Lys Ile# 20- Ser Cys Lys Ala Ser Gly Tyr Thr Phe Thr As - #p Tyr Asn Met Asp Trp# 35- Val Lys Gln Ser His Gly Lys Ser Leu Glu Tr - #p Ile Gly Tyr Ile Tyr# 50- Pro Asn Asn Gly Gly Thr Gly Tyr Asn Gln Ly - #s Phe Lys Ser Lys Ala# 65- Thr Leu Thr Val Asp Lys Ser Ser Ser Thr Al - #a Tyr Met Glu Leu His# 80- Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr Ty - #r Cys Ala Thr Tyr Gly#100- His Tyr Tyr Gly Tyr Met Phe Ala Tyr Trp Gl - #y Gln Gly Thr Leu Val# 115- Thr Val Ser Ala 120- (2) INFORMATION FOR SEQ ID NO:92:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 129 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide22..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: BY SIMILA - #RITY WITH KNOWN SEQUENCE TO TO AN#CONSENSUS ESTABLISHED- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 24..33 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 1"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 49..55 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 2"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 88..96 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 3"- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:92:- Met His Phe Gln Val Gln Il - #e Phe Ser Phe Leu Leu Ile Ser10- Ala Ser Val Ile Met Ser Arg Gly Gln Ile Va - #l Leu Thr Gln Ser Pro# 5 1- Ala Ile Met Ser Ala Ser Pro Gly Glu Lys Va - #l Thr Ile Thr Cys Ser# 20- Ala Ser Ser Ser Val Ser Tyr Met His Trp Ph - #e Gln Gln Lys Pro Gly# 40- Thr Ser Pro Lys Leu Trp Ile Tyr Ser Thr Se - #r Asn Leu Ala Ser Gly# 55- Val Pro Ala Arg Phe Ser Gly Ser Gly Ser Gl - #y Thr Ser Tyr Ser Leu# 70- Thr Ile Ser Arg Met Glu Ala Glu Asp Ala Al - #a Thr Tyr Tyr Cys Gln# 85- Gln Arg Ser Ser Tyr Pro Tyr Thr Phe Gly Gl - #y Gly Thr Lys Leu Glu# 100- Ile Lys Arg105- (2) INFORMATION FOR SEQ ID NO:93:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 137 amino (B) TYPE: amino acids (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide19..-1 (B) LOCATION: (C) IDENTIFICATION METHOD: BY SIMILA - #RITY WITH KNOWN SEQUENCE OR TO AN#CONSENSUS ESTABLISHED- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 31..35 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 1"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 55..66 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISHED CONSENSUS#/product= "HYPERVARIABLE REGION 2"- (ix) FEATURE: (A) NAME/KEY: domain (B) LOCATION: 99..107 (C) IDENTIFICATION METHOD: - # BY SIMILARITY WITH KNOW - #N SEQUENCE OR TO AN ESTABLISEHD CONSENSUS#/product= "HYPERVARIABLE REGION 3"- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:93:#Met Gly Trp Ser Trp Ile Phe15- Leu Phe Leu Leu Ser Gly Thr Ala Gly Val Le - #u Ser Glu Val Gln Leu# 1- Gln Gln Ser Gly Pro Glu Leu Val Lys Pro Gl - #y Ala Ser Val Lys Ile# 20- Ser Cys Lys Ala Ser Gly Tyr Thr Phe Thr As - #p Tyr Asn Met Asp Trp# 35- Val Lys Gln Ser His Gly Lys Ser Leu Glu Tr - #p Ile Gly Tyr Ile Tyr# 50- Pro Asn Asn Gly Gly Thr Gly Tyr Asn Gln Ly - #s Phe Lys Ser Lys Ala# 65- Thr Leu Thr Val Asp Lys Ser Ser Ser Thr Al - #a Tyr Met Glu Leu His# 80- Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr Ty - #r Cys Ala Arg Ala Gly#100- Arg Tyr Tyr Tyr Ala Trp Asp Trp Gly Gln Gl - #y Thr Leu Val Thr Val# 115- Ser Ala- (2) INFORMATION FOR SEQ ID NO:94:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 5 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:94:- Asp Tyr Asn Met Asp 1 5- (2) INFORMATION FOR SEQ ID NO:95:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 17 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:95:- Tyr Ile Tyr Pro Asn Asn Gly Gly Thr Gly Ty - #r Asn Gln Lys Phe Lys# 15- Ser- (2) INFORMATION FOR SEQ ID NO:96:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 11 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:96:- Tyr Gly His Tyr Tyr Gly Tyr Met Phe Ala Ty - #r# 10- (2) INFORMATION FOR SEQ ID NO:97:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 10 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:97:- Ser Ala Ser Ser Ser Val Ser Tyr Met His# 10- (2) INFORMATION FOR SEQ ID NO:98:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 7 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:98:- Ser Thr Ser Asn Leu Ala Ser 1 5- (2) INFORMATION FOR SEQ ID NO:99:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 9 amino (B) TYPE: amino acids (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:99:- Gln Gln Arg Ser Ser Tyr Pro Tyr Thr 1 5- (2) INFORMATION FOR SEQ ID NO:100:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 144 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:100:#Ile Phe Leu Phe Leu Leu Ser Gly10- Thr Ala Gly Val Leu Ser Gln Val Gln Leu Gl - #n Glu Ser Gly Pro Gly# 10- Leu Val Arg Pro Ser Gln Thr Leu Ser Leu Th - #r Cys Thr Val Ser Gly# 25- Phe Thr Phe Ser Asp Tyr Asn Met Asp Trp Va - #l Arg Gln Pro Pro Gly# 40- Arg Gly Leu Glu Trp Ile Gly Tyr Ile Tyr Pr - #o Asn Asn Gly Gly Thr# 55- Gly Tyr Asn Gln Lys Phe Lys Ser Arg Val Th - #r Met Leu Val Asp Thr# 70- Ser Lys Asn Gln Phe Ser Leu Arg Leu Ser Se - #r Val Thr Ala Ala Asp# 90- Thr Ala Val Tyr Tyr Cys Ala Arg Tyr Gly Hi - #s Tyr Tyr Gly Tyr Met# 105- Phe Ala Tyr Trp Gly Gln Gly Thr Thr Val Th - #r Val Ser Ser Ala Ser# 120- Thr Lys Gly 125- (2) INFORMATION FOR SEQ ID NO:101:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 133 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:101:- Met His Phe Gln Val G - #ln Ile Phe Ser Phe Leu Leu Ile Ser10- Ala Ser Val Ile Met Ser Arg Gly Asp Ile Gl - #n Leu Thr Gln Ser Pro# 5 1- Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Va - #l Thr Ile Thr Cys Ser# 20- Ala Ser Ser Ser Val Ser Tyr Met His Trp Ty - #r Gln Gln Lys Pro Gly# 40- Lys Ala Pro Lys Leu Leu Ile Tyr Ser Thr Se - #r Asn Leu Ala Ser Gly# 55- Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gl - #y Thr Asp Phe Thr Phe# 70- Thr Ile Ser Ser Leu Gln Pro Glu Asp Ile Al - #a Thr Tyr Tyr Cys Gln# 85- Gln Arg Ser Ser Tyr Pro Tyr Thr Phe Gly Gl - #y Gly Thr Lys Val Glu# 100- Ile Lys Arg Thr Val Ala Ala105 1 - #10- (2) INFORMATION FOR SEQ ID NO:102:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 27 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:102:# 27 CACC ATCTGTC- (2) INFORMATION FOR SEQ ID NO:103:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 27 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic DNA"RIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:103:# 27 CACC ATCTGTC__________________________________________________________________________

Number	Date	Country
314 161	May 1989	EPX
533 199	Mar 1993	EPX

Humanized antibodies to ganglioside GM.sub.2

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Foreign Referenced Citations (2)

Non-Patent Literature Citations (29)

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Entry
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