Tagawa K, Sendai N, Ohno K, Kawaguchi T, Kitano H, Matsunaga T
Department of Chemical and Biochemical Engineering, Toyama Univesity, Japan.
Bioconjug Chem. 1999 May-Jun;10(3):354-60. doi: 10.1021/bc980083x.
Novel amphiphiles which carry many mannose residues as side chains were prepared by telomerization of N-methacryloylaminopropyl D-mannopyranoside (alpha:beta = 20:1), N-methacryloylaminohexyl D-mannopyranoside (alpha:beta = 20:1), or 3-(2-methacryloylaminoethylthio)propyl D-mannopyranoside (alpha:beta = 4:1) using a lipophilic radical initiator. The mannose-carrying amphiphiles incorporated in liposomes were recognized by a lectin from Canavalia ensiformis (Con A), which was proven by the increase in turbidity of the liposome suspension after mixing with Con A. The interaction between sugar residues on the liposome surface and the lectin was largely affected by the degree of polymerization (DP) and the surface density of the amphiphile in the liposomes. The distance between the sugar residues and the polymer main chain did not affect the specific recognition by the lectin significantly in the liposome system, whereas it appreciably affected the recognition in the water-soluble polymer system. The association constants (Ka) of the amphiphiles (DP approximately 18) with Con A (0.3-2.2 x 10(6) M-1 at 25 degrees C) were much larger than that of alpha-methyl D-mannopyranoside (8.2 x 10(3) M-1) due to the "cluster effect ". The positive entropy change (20-52 J/mol K) for the binding of Con A to mannose residues on the liposome surface showed that the recognition in the liposome system was largely promoted by the release of water molecules from both the sugar residues on the liposome surface and the binding site of Con A.
通过使用亲脂性自由基引发剂对N-甲基丙烯酰氨基丙基D-甘露吡喃糖苷(α:β = 20:1)、N-甲基丙烯酰氨基己基D-甘露吡喃糖苷(α:β = 20:1)或3-(2-甲基丙烯酰氨基乙硫基)丙基D-甘露吡喃糖苷(α:β = 4:1)进行端粒化反应,制备了带有许多甘露糖残基作为侧链的新型两亲分子。包封在脂质体中的携带甘露糖的两亲分子可被来自刀豆(Con A)的凝集素识别,这通过与Con A混合后脂质体悬浮液浊度的增加得到证实。脂质体表面糖残基与凝集素之间的相互作用在很大程度上受聚合度(DP)和脂质体中两亲分子的表面密度影响。在脂质体体系中,糖残基与聚合物主链之间的距离对凝集素的特异性识别影响不大,而在水溶性聚合物体系中则有明显影响。由于“簇效应”,两亲分子(DP约为18)与Con A在25℃时的缔合常数(Ka)(0.3 - 2.2×10⁶ M⁻¹)远大于α-甲基D-甘露吡喃糖苷(8.2×10³ M⁻¹)。Con A与脂质体表面甘露糖残基结合的正熵变(20 - 52 J/mol K)表明,脂质体体系中的识别很大程度上是由脂质体表面糖残基和Con A结合位点释放水分子所促进的。