Fig. 5.
Fig. 5. Schematic map of the different shapes of the haptoglobin polymers as determined by phenotype. / These shapes have been confirmed by electron microscopic analysis of haptoglobin purified from patients with haptoglobin 1-1, 2-1, or 2-2.20 Critical disulfide linkages necessary for covalent cross-linking of haptoglobin monomers (circles) to form polymers are found on exons 3 and 4 (α-chain of haptoglobin). The haptoglobin 2 allele has a duplication of exons 3 and 4. The haptoglobin 1 monomer is monovalent (note single arrow) and thus can only associate with one other haptoglobin molecule to create dimers. The haptoglobin 2 monomer is bivalent (note 2 arrows) and can associate with 2 different haptoglobin monomers. Consequently, the haptoglobin in persons homozygous for the 2 allele will be cyclic polymers.

Schematic map of the different shapes of the haptoglobin polymers as determined by phenotype.

These shapes have been confirmed by electron microscopic analysis of haptoglobin purified from patients with haptoglobin 1-1, 2-1, or 2-2.20 Critical disulfide linkages necessary for covalent cross-linking of haptoglobin monomers (circles) to form polymers are found on exons 3 and 4 (α-chain of haptoglobin). The haptoglobin 2 allele has a duplication of exons 3 and 4. The haptoglobin 1 monomer is monovalent (note single arrow) and thus can only associate with one other haptoglobin molecule to create dimers. The haptoglobin 2 monomer is bivalent (note 2 arrows) and can associate with 2 different haptoglobin monomers. Consequently, the haptoglobin in persons homozygous for the 2 allele will be cyclic polymers.

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