ELISA for Determination of the Haptoglobin Pheno - type , Nina

The haptoglobin genetic locus at 16q22 is polymorphic with two known classes of alleles, denoted 1 and 2 (1 ). The polymorphism is extremely common, with worldwide frequencies of the two alleles being approximately equal. However, there is considerable geographic and ethnic variation in the distribution of haptoglobin phenotypes (1 ). Over the past 3–4 years our laboratory has demonstrated that haptoglobin is a major susceptibility gene for the development of diabetic vascular complications in multiple longitudinal and cross-sectional population studies (2–13). Diabetic individuals homozygous for the haptoglobin 2 allele were shown to be at five times greater risk of developing cardiovascular disease compared with diabetic individuals homozygous for the haptoglobin 1 allele, with an intermediate risk for the heterozygote (8 ). The increased susceptibility to vascular complications conferred by the Hp 2 allele has recently been recapitulated in a transgenic animal model, which showed direct linkage of the polymorphism with disease susceptibility (R. Lotan et al., manuscript submitted). Mechanistic studies using the purified protein products of the Hp 1 and Hp 2 alleles have identified profound differences in antioxidant and immunomodulatory activity (14, 15). Functional as well as structural differences exist between the various haptoglobin allelic protein products (1 ). The Hp 2 allele appears to have arisen by an intragenic duplication event of exons 3 and 4 of the Hp 1 allele, which leads to the duplication of a multimerization domain in exon 3. Consequently, the Hp 1 allele protein product forms dimers only. The Hp 2 allele has two copies of exon 3; therefore, Hp 2 allele protein products combine to form cyclic polymers three monomers and larger in size. In heterozygotes, linear polymers containing both allelic protein products have been observed. A variety of techniques have been developed to type individuals for the haptoglobin polymorphism. HPLC and starch, polyacrylamide, and agarose gel electrophoresis methods rely on differences in the molecular sizes of the haptoglobin protein products (1-1, 2-1, or 2-2) for typing (1, 16). Recently, a PCR-based approach has been described for haptoglobin typing with complete correspondence between the DNAand protein-based methods (17 ). The development of an antibody-based ELISA test to type haptoglobin has been hampered by the apparent lack of antigenic determinants unique to either allelic protein product. Apart from a single junction at the site of duplication of exon 3, there exist no differences in primary amino acid sequence between the haptoglobin alleles. However, because of the unique polymeric differences among the protein types (dimers vs linear polymers vs cyclic polymers), we proposed that it would be feasible to develop a single-chain antibody that could be used in an ELISA to reliably differentiate among haptoglobin phenotypes. We constructed a single-chain Fv (scFv) library from spleen mRNA isolated from C57Bl/6 mice immunized with human Hp 2-2 protein. (Mice have only one allele for haptoglobin, corresponding to the Hp 1 allele). Briefly, the scFv repertoire was prepared from mRNA by reverse transcription-PCR (18, 19). The reverse transcription-PCR product was cloned as a SfiI-Not1 fragment into the pCANTAB6 phagemid vector, which produced a myc tag fused to the COOH terminus of the scFv gene. The complexity of the library was 1.5 10 independent clones. Clones specific for Hp 2-2 were selected by incubating 10 colony-forming units of the library in immunotubes (Nunc) coated with Hp 2-2. After extensive washing, bound phages were eluted with triethylamine and expanded in Escherichia coli TG1 cells subsequently superinfected with M13KO7 helper phage (19 ). Panning was repeated six times, with excess Hp 1-1 present in the final three rounds to select for phage clones specific for Hp 2-2. After the panning process, individual phage clones were screened by ELISA. Phage clone E3 bound immobilized Hp 2-2 substantially better than Hp 1-1. Purified single-chain E3-myc antibody, when tested in an ELISA against immobilized Hp 1-1 or Hp 2-2 and developed with horseradish peroxidase-conjugated anti-myc secondary antibody, gave a fourfold greater signal with Hp 2-2 than with Hp 1-1. This difference between Hp 1-1 and Hp 2-2 was amplified by use of E3 in a sandwich format because of the different polymeric structures of the haptoglobin proteins. Hp 1-1 dimers have only two antigenic sites recognized by E3, whereas Hp 2-2 polymers have three or more antigenic sites. Binding of both sites of a dimer to E3 immobilized to the microwell will prevent binding of the second E3 antibody used to generate the ELISA signal. Such a blocking event by the first capture antibody is less likely to occur as the number of polymeric units in the Hp protein increases, thus giving rise to a greater signal when Hp 2-1 or Hp 2-2 is present. For the sandwich ELISA we generated an E3 capture antibody without the myc tag. For reasons of convenience, the phagemid insert encoding E3 was subcloned into the pCANTAB5E vector, which led to E3 coupled to an E protein tag. However, the capture antibody need not have any tag at all. The protocol for the developed sandwich ELISA for haptoglobin phenotype determination is as follows. Microtiter plates (Maxisorb; Nunc) are coated with 100 L/well of E3 Etag antibody (10 mg/L in coating buffer) overnight at 4 °C. The wells are washed with Tris-buffered saline containing 0.5 mL/L Tween and then incubated with 150 L/well blocking buffer (Tris-buffered saline containing 10 g/L bovine serum albumin and 1 mL/L Tween) for 1–2 h at 37 °C. Serum samples diluted 1:100 in blocking buffer were added to the wells (100 L) and incubated for 1 h at room temperature. After washTechnical Briefs