TY - JOUR
T1 - Structure of the liposome composed of lipid-heme and phospholipids
AU - Yuasa, Makoto
AU - Aiba, Kazukiyo
AU - Ogata, Yoshitaka
AU - Nishide, Hiroyuki
AU - Tsuchida, Eishun
PY - 1986/9/11
Y1 - 1986/9/11
N2 - The amphiphilic heme derivative, 5,10,15,20-tetra(α,α,α,α-o-(2′,2′-dimethyl-20′-(2′-trimethylammonioethyl) phosphonatoxyicosanamido)pheny)phorphinatoiron(II) (lipid-heme), formed a stable liposome (Φ ≈ 400 Å) with phospholipids. Differential scanning calorimetry showed that incorporation of the lipid-heme in the liposome bilayer (lipid/lipid-heme > 25) causes no disordering of the bilayer structure. Ligation of a bulky ligand to the lipid-heme liposome indicated that the lipid-heme situates facing predominantly outwards in the liposome. The closed vesicle structure and the stability of the lipid-heme liposome were also confirmed by the encapsulating capability of the fluorescence compound.
AB - The amphiphilic heme derivative, 5,10,15,20-tetra(α,α,α,α-o-(2′,2′-dimethyl-20′-(2′-trimethylammonioethyl) phosphonatoxyicosanamido)pheny)phorphinatoiron(II) (lipid-heme), formed a stable liposome (Φ ≈ 400 Å) with phospholipids. Differential scanning calorimetry showed that incorporation of the lipid-heme in the liposome bilayer (lipid/lipid-heme > 25) causes no disordering of the bilayer structure. Ligation of a bulky ligand to the lipid-heme liposome indicated that the lipid-heme situates facing predominantly outwards in the liposome. The closed vesicle structure and the stability of the lipid-heme liposome were also confirmed by the encapsulating capability of the fluorescence compound.
KW - Heme
KW - Hemoglobin model
KW - Lipid-heme
KW - Liposome
KW - Oxygen carrier
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U2 - 10.1016/0005-2736(86)90553-5
DO - 10.1016/0005-2736(86)90553-5
M3 - Article
AN - SCOPUS:0022553764
SN - 0005-2736
VL - 860
SP - 558
EP - 565
JO - Biochimica et Biophysica Acta - Biomembranes
JF - Biochimica et Biophysica Acta - Biomembranes
IS - 3
ER -