19 research outputs found
Interaction of the human erythrocyte Band 3 anion exchanger 1 (AE1, SLC4A1) with lipids and glycophorin A: Molecular organization of the Wright (Wr) blood group antigen
The Band 3 (AE1, SLC4A1) membrane protein is found in red blood cells and in kidney where it functions as an electro-neutral chloride/bicarbonate exchanger. In this study, we have used molecular dynamics simulations to provide the first realistic model of the dimeric membrane domain of human Band 3 in an asymmetric lipid bilayer containing a full complement of phospholipids, including phosphatidylinositol 4,5–bisphosphate (PIP2) and cholesterol, and its partner membrane protein Glycophorin A (GPA). The simulations show that the annular layer in the inner leaflet surrounding Band 3 was enriched in phosphatidylserine and PIP2 molecules. Cholesterol was also enriched around Band 3 but also at the dimer interface. The interaction of these lipids with specific sites on Band 3 may play a role in the folding and function of this anion transport membrane protein. GPA associates with Band 3 to form the Wright (Wr) blood group antigen, an interaction that involves an ionic bond between Glu658 in Band 3 and Arg61 in GPA. We were able to recreate this complex by performing simulations to allow the dimeric transmembrane portion of GPA to interact with Band 3 in a model membrane. Large-scale simulations showed that the GPA dimer can bridge Band 3 dimers resulting in the dynamic formation of long strands of alternating Band 3 and GPA dimers
Organization and dynamics of the red blood cell Band 3 anion exchanger SLC4A1: Insights from molecular dynamic simulations
Effect of the Southeast Asian ovalocytosis deletion on the conformational dynamics of the signal- anchor transmembrane segment 1 of the red cell anion exchanger 1 (AE1, Band 3, SLC4A1)
The first transmembrane (TM1) helix in the red cell anion exchanger (AE1, Band 3, SLC4A1) acts as an internal signal anchor that binds the signal recognition particle and directs the nascent polypeptide chain to the endoplasmic reticulum (ER) membrane where it moves from the translocon laterally into the lipid bilayer. The sequence N-terminal to TM1 forms an amphipathic helix that lies at the membrane interface connected to TM1 by a bend at Pro403. Southeast Asian Ovalocytosis (SAO) is a red cell abnormality caused by a nine-amino acid deletion (Ala400-Ala408) at the N-terminus of TM1. Here we demonstrate, by extensive (~4.5 μs) of molecular dynamics simulations of TM1 in a model 1-palmitoyl-2-oleoyl-sn-glycero-3- phosphocholine (POPC) membrane, that the isolated TM1 peptide is highly dynamic and samples the structure of TM1 seen in the crystal structure of the membrane domain of AE1. The SAO deletion not only removes the proline-induced bend but also causes a “pulling in” of the part of the amphipathic helix into the hydrophobic phase of the bilayer, as well as the C-terminal of the peptide. The dynamics of the SAO peptide very infrequently resembles the structure of TM1 in AE1, demonstrating the disruptive effect the SAO deletion has on AE1 folding. These results provide a precise molecular view of the disposition and dynamics of the wild-type and SAO TM1 in a lipid bilayer, an important early biosynthetic intermediate in the insertion of AE1 into the ER membrane that extend earlier results of cell-free translation experiments
Effect of the Southeast Asian ovalocytosis deletion on the conformational dynamics of the signal- anchor transmembrane segment 1 of the red cell anion exchanger 1 (AE1, Band 3, SLC4A1)
The first transmembrane (TM1) helix in the red cell anion exchanger (AE1, Band 3, SLC4A1)
acts as an internal signal anchor that binds the signal recognition particle and directs the nascent
polypeptide chain to the endoplasmic reticulum (ER) membrane where it moves from the
translocon laterally into the lipid bilayer. The sequence N-terminal to TM1 forms an
amphipathic helix that lies at the membrane interface connected to TM1 by a bend at Pro403.
Southeast Asian Ovalocytosis (SAO) is a red cell abnormality caused by a nine-amino acid
deletion (Ala400-Ala408) at the N-terminus of TM1. Here we demonstrate, by extensive (~4.5
μs) of molecular dynamics simulations of TM1 in a model 1-palmitoyl-2-oleoyl-sn-glycero-3-
phosphocholine (POPC) membrane, that the isolated TM1 peptide is highly dynamic and
samples the structure of TM1 seen in the crystal structure of the membrane domain of AE1. The
SAO deletion not only removes the proline-induced bend but also causes a “pulling in” of the
part of the amphipathic helix into the hydrophobic phase of the bilayer, as well as the C-terminal
of the peptide. The dynamics of the SAO peptide very infrequently resembles the structure of
TM1 in AE1, demonstrating the disruptive effect the SAO deletion has on AE1 folding. These
results provide a precise molecular view of the disposition and dynamics of the wild-type and
SAO TM1 in a lipid bilayer, an important early biosynthetic intermediate in the insertion of AE1
into the ER membrane that extend earlier results of cell-free translation experiments
Molecular Simulations of Intact Anion Exchanger 1 Reveal Specific Domain and Lipid Interactions
Anion exchanger 1 (AE1) is responsible for the exchange of bicarbonate and chloride across the erythrocyte plasma membrane. Human AE1 consists of a cytoplasmic and a membrane domain joined by a 33-residue flexible linker. Crystal structures of the individual domains have been determined, but the intact AE1 structure remains elusive. In this study, we use molecular dynamics simulations and modeling to build intact AE1 structures in a complex lipid bilayer that resembles the native erythrocyte plasma membrane. AE1 models were evaluated using available experimental data to provide an atomistic view of the interaction and dynamics of the cytoplasmic domain, the membrane domain, and the connecting linker in a complete model of AE1 in a lipid bilayer. Anionic lipids were found to interact strongly with AE1 at specific amino acid residues that are linked to diseases and blood group antigens. Cholesterol was found in the dimeric interface of AE1, suggesting that it may regulate subunit interactions and anion transport
Band 3, the human red cell chloride/bicarbonate anion exchanger (AE1, SLC4A1), in a structural context
The crystal structure of the dimeric membrane domain of human Band 31, the red cell chloride/bicarbonate anion exchanger 1 (AE1, SLC4A1), provides a structural context for over four decades of studies into this historic and important membrane glycoprotein. In this review, we highlight the key structural features responsible for anion binding and translocation and have integrated the following topological markers within the Band 3 structure: blood group antigens, N-glycosylation site, protease cleavage sites, inhibitor and chemical labeling sites, and the results of scanning cysteine and N-glycosylation mutagenesis. Locations of mutations linked to human disease, including those responsible for Southeast Asian ovalocytosis, hereditary stomatocytosis, hereditary spherocytosis, and distal renal tubular acidosis, provide molecular insights into their effect on Band 3 folding. Finally, molecular dynamics simulations of phosphatidylcholine self-assembled around Band 3 provide a view of this membrane protein within a lipid bilayer