Probing the Importance of the Amino-Terminal Sequence of the β- and γ-Chains to the Properties of Normal Adult and Fetal Hemoglobins

• Published in: Biochemistry (Easton) Vol. 40; no. 40; pp. 12169 - 12177
• Main Authors: Tsai, Ching-Hsuan, Larson, Sandra C, Shen, Tong-Jian, Ho, Nancy T, Fisher, Gregory W, Tam, Ming F, Ho, Chien
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 09-10-2001
• Subjects: Adult; Base Sequence; DNA Primers; Hemoglobins - chemistry; Hemoglobins - genetics; Hemoglobins - metabolism; Humans; Molecular Probes; Mutation; Nuclear Magnetic Resonance, Biomolecular; Protein Denaturation; Recombinant Proteins - chemistry; Recombinant Proteins - genetics; Recombinant Proteins - metabolism
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi0111045

A recombinant mutant of human fetal hemoglobin (Hb F), named rHb Oscar, has been constructed to explore the importance of the sequence of the amino-terminal region of the γ-chain to the structural and functional properties of Hb F as compared to human normal adult hemoglobin (Hb A). Substitutions in the N-terminal region of Hb A have shown this region to be important to its structural and functional properties. Recent studies of recombinant mutants of Hb A with γ-chain mutations have been used to probe the significance of the N-terminal sequence to the properties of Hb F. One of these mutants of Hb A, called rHb Felix, contains eight substitutions in the N-terminal region of the β-chain corresponding to the sequence of the γ-chain in that region [Dumoulin et al. (1998) J. Biol. Chem. 273, 35032−35038]. rHb Felix exhibits a 2,3-bisphosphoglycerate (2,3-BPG) response like that of Hb A, but its tetramer−dimer dissociation constant is similar to that of Hb F. In contrast, rHb Oscar contains a γ-chain with eight mutations at the N-terminal end corresponding to the sequence of the β-chain of Hb A in that region. 1H NMR studies of rHb Oscar indicate a global structure like that of Hb F. rHb Oscar is not as stable against alkaline denaturation as Hb F but is more stable than Hb A, and it exhibits a stronger response to 2,3-BPG and inositol hexaphosphate as compared to Hb F. The 2,3-BPG effect in rHb Oscar also appears to be slightly enhanced compared to that in Hb A. Subzero isoelectric focusing experiments suggest that rHb Oscar does not have dissociation properties like those of Hb A. These results along with those of rHb Felix illustrate that the effects of the N-terminal region on structure and function of the Hb molecule are complicated by interactions with the rest of the molecule that are not yet well defined. However, studies of complementary mutations of Hb A and Hb F may eventually help to define such interactions and lead to a better understanding of the relationship between the amino acid sequence and the properties of the Hb molecule.