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Blood, 15 December 2005, Vol. 106, No. 13, pp. 4359-4366.
Prepublished online as a Blood First Edition Paper on August 23, 2005August 25, 2005; DOI 10.1182/blood-2005-07-2806.


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Submitted July 14, 2005
Accepted August 12, 2005

The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function

Silverio Perrotta*, Adriana Borriello, Andrea Scaloni, Lucia De Franceschi, Anna Maria Brunati, Francesco Turrini, Vincenzo Nigro, Emanuele Miraglia del Giudice, Bruno Nobili, Maria Luisa Conte, Francesca Rossi, Achille Iolascon, Arianna Donella-Deana, Vincenzo Zappia, Vincenzo Poggi, William Anong, Philip Low, Narla Mohandas, and Fulvio Della Ragione

Department of Pediatrics, Second University of Naples, Naples, Italy
Department of Biochemistry and Biophysics "F. Cedrangolo", Second University of Naples, Naples, Italy
Proteomics and Mass Spectrometry Laboratory, I.S.P.A.A.M., National Research Council, Naples, Italy
Clinical and Experimental Medicine, University of Verona, Verona, Italy
Department of Biochemistry, University of Padova, Padova, Italy
Biology, Genetics and Medicinal Chemistry, University of Torino, Torino, Italy
Dipartimento di Patologia Generale, Second University of Naples and TIGEM, Naples, Italy
Medical Genetics, University Federico II, CEINGE, Naples, Italy
Pediatric Hematology-Oncology, Pausillipon Hospital, Naples, Italy
Department of Chemistry, Purdue University, West Lafayette, IN, USA
New York Blood Center, New York, NY, USA

* Corresponding author; email: silverio.perrotta{at}unina2.it.

The 911 amino acid band 3 (SLC4A1) is the major intrinsic membrane protein of red cells and is the principal Cl-/HCO3- exchanger. The N-terminal cytoplasmic domain of band 3 anchors the spectrin-based membrane skeleton to the lipid bilayer through its interaction with ankyrin and also binds glycolytic enzymes and hemoglobin. We identified a son of consanguineous marriage with severe anemia in association with marked deficiency of band 3 (12±4% of normal). Direct nucleotide sequencing of SLC4A1 gene demonstrated a single base substitution (T->C) at position +2 in the donor splice site of intron 2 resulting in the generation of a novel mutant protein. Biochemical characterization of the mutant protein showed that it lacked the first 11 N-terminal amino acids (Band 3 "Neapolis"). The expression of the mutant protein resulted in the complete absence of membrane bound aldolase and the mutant band 3 could not be tyrosine phosphorylated. The ability of the malarial parasite, P. falciparum, to invade these red cells was significantly decreased. The identification of a novel band 3 mutant and its structural and functional characterization enabled us to identify pivotal roles for the 11 N-terminal amino acids in several protein functions and, in turn, in red cell physiology.


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