Institut des Biomolécules Max Mousseron, CNRS, Université Montpellier 1, Université Montpellier 2, DSBC, C.C. 1706, place Eugène Bataillon, 34095 Montpellier cedex 5, France.
Chemistry. 2010 Feb 15;16(7):2309-16. doi: 10.1002/chem.200901734.
The synthesis and characterisation of new arborescent architectures of poly(L-lysine), called lysine dendrigraft (DGL) polymers, are described. DGL polymers were prepared through a multiple-generation scheme (up to generation 5) in a weakly acidic aqueous medium by polycondensing N(epsilon)-trifluoroacetyl-L-lysine-N-carboxyanhydride (Lys(Tfa)-NCA) onto the previous generation G(n-1) of DGL, which was used as a macroinitiator. The first generation employed spontaneous NCA polycondensation in water without a macroinitiator; this afforded low-molecular-weight, linear poly(L-lysine) G1 with a polymerisation degree of 8 and a polydispersity index of 1.2. The spontaneous precipitation of the growing N(epsilon)-Tfa-protected polymer (GnP) ensures moderate control of the molecular weight (with unimodal distribution) and easy work-up. The subsequent alkaline removal of Tfa protecting groups afforded generation Gn of DGL as a free form (with 35-60% overall yield from NCA precursor, depending on the DGL generation) that was either used directly in the synthesis of the next generation (G(n+1)) or collected for other uses. Unprotected forms of DGL G1-G5 were characterised by size-exclusion chromatography, capillary electrophoresis and (1)H NMR spectroscopy. The latter technique allowed us to assess the branching density of DGL, the degree of which (ca. 25%) turned out to be intermediate between previously described dendritic graft poly(L-lysines) and lysine dendrimers. An optimised monomer (NCA) versus macroinitiator (DGL G(n-1)) ratio allowed us to obtain unimodal molecular weight distributions with polydispersity indexes ranging from 1.3 to 1.5. Together with the possibility of reaching high molecular weights (with a polymerisation degree of ca. 1000 for G5) within a few synthetic steps, this synthetic route to DGL provides an easy, cost-efficient, multigram-scale access to dendritic polylysines with various potential applications in biology and in other domains.
描述了一种新的树枝状聚(L-赖氨酸)结构,称为赖氨酸树枝状聚合物(DGL)的合成和表征。DGL 聚合物是通过在弱酸性水介质中通过多代方案(最多至第 5 代)制备的,通过将 N(epsilon)-三氟乙酰基-L-赖氨酸-N-羧酸酐(Lys(Tfa)-NCA)缩聚到前一代 DGL 的 G(n-1)上,前一代 DGL 用作大分子引发剂。第一代在没有大分子引发剂的情况下在水中自发进行 NCA 缩聚,得到低分子量、线性聚(L-赖氨酸)G1,聚合度为 8,多分散指数为 1.2。生长的 N(epsilon)-Tfa 保护聚合物(GnP)的自发沉淀确保了分子量的适度控制(具有单峰分布)和易于处理。随后用碱去除 Tfa 保护基团,得到 DGL 的 Gn 代作为游离形式(NCA 前体的总收率为 35-60%,具体取决于 DGL 代),可直接用于下一代(G(n+1))的合成,或收集用于其他用途。通过尺寸排阻色谱、毛细管电泳和(1)H NMR 光谱对未保护形式的 DGL G1-G5 进行了表征。后者技术使我们能够评估 DGL 的支化密度,其程度(约 25%)介于先前描述的树枝状接枝聚(L-赖氨酸)和赖氨酸树枝状聚合物之间。优化的单体(NCA)与大分子引发剂(DGL G(n-1))的比例允许我们获得单峰分子量分布,多分散指数范围从 1.3 到 1.5。与在几个合成步骤内达到高分子量(G5 的聚合度约为 1000)的可能性相结合,这种 DGL 的合成途径为具有各种生物学和其他领域潜在应用的各种树枝状聚赖氨酸提供了一种简单、经济高效、多克规模的方法。