Human haptoglobin structure and function - A molecular modelling study

F. Polticelli, A. Bocedi, G. Minervini, P. Ascenzi

Research output: Contribution to journalArticle

49 Citations (Scopus)

Abstract

Hemoglobin is the most prominent protein in blood, transporting O 2 and facilitating reactive oxygen and nitrogen species detoxification. Hemoglobin metabolism leads to the release of extra-erythrocytic hemoglobin, with potentially severe consequences for health. Extra-erythrocytic hemoglobin is complexed to haptoglobin for clearance by tissue macrophages. The human gene for haptoglobin consists of three structural alleles: Hp1F, Hp1S and Hp2. The products of the Hp1F and Hp1S alleles differ by only one amino acid, whereas the Hp2 allele is the result of a fusion of the Hp1F and Hp1S alleles, is present only in humans and gives rise to a longer α-chain. Haptoglobin consists of a dimer of αβ-chains covalently linked by a disulphide bond between the Cys15 residue of each α-chain. However, the presence of the Hp1 and Hp2 alleles in humans gives rise to HPT1-1 dimers (covalently linked by Cys15 residues), HPT1-2 hetero-oligomers and HPT2-2 oligomers. In fact, the HPT2 variant displays two free Cys residues (Cys15 and Cys74) whose participation in intermolecular disulphide bonds gives rise to higher-order covalent multimers. Here, the complete modelling of both haptoglobin variants, together with their basic quaternary structure arrangements (i.e. HPT1 dimer and HPT2 trimer), is reported. The structural details of the models, which represent the first complete view of the molecular details of human haptoglobin variants, are discussed in relation to the known haptoglobin function(s).

Original languageEnglish
Pages (from-to)5648-5656
Number of pages9
JournalFEBS Journal
Volume275
Issue number22
DOIs
Publication statusPublished - Nov 2008

Fingerprint

Haptoglobins
Molecular modeling
Alleles
Hemoglobins
Dimers
Oligomers
Disulfides
Reactive Nitrogen Species
Detoxification
Macrophages
Structural Models
Metabolism
Blood Proteins
Reactive Oxygen Species
Blood
Fusion reactions
Genes
human HP protein
Health
Tissue

Keywords

  • Chaperone-like activity
  • Covalent multimers
  • Haemoglobin
  • Haptoglobin
  • Homology modelling

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology

Cite this

Polticelli, F., Bocedi, A., Minervini, G., & Ascenzi, P. (2008). Human haptoglobin structure and function - A molecular modelling study. FEBS Journal, 275(22), 5648-5656. https://doi.org/10.1111/j.1742-4658.2008.06690.x

Human haptoglobin structure and function - A molecular modelling study. / Polticelli, F.; Bocedi, A.; Minervini, G.; Ascenzi, P.

In: FEBS Journal, Vol. 275, No. 22, 11.2008, p. 5648-5656.

Research output: Contribution to journalArticle

Polticelli, F, Bocedi, A, Minervini, G & Ascenzi, P 2008, 'Human haptoglobin structure and function - A molecular modelling study', FEBS Journal, vol. 275, no. 22, pp. 5648-5656. https://doi.org/10.1111/j.1742-4658.2008.06690.x
Polticelli, F. ; Bocedi, A. ; Minervini, G. ; Ascenzi, P. / Human haptoglobin structure and function - A molecular modelling study. In: FEBS Journal. 2008 ; Vol. 275, No. 22. pp. 5648-5656.
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