Department of Chemistry, University of California, Irvine, California 92697, USA.
J Am Chem Soc. 2009 Nov 18;131(45):16454-60. doi: 10.1021/ja9050873.
M13 phage have provided scaffolds for nanostructure synthesis based upon self-assembled inorganic and hard materials interacting with phage-displayed peptides. Additionally, phage display has been used to identify binders to plastic, TiO(2), and other surfaces. However, synthesis of phage-based materials through the hybridization of soft materials with the phage surface remains unexplored. Here, we present an efficient "phage wrapping" strategy for the facile synthesis of phage coated with soluble, cationic polymers. Polymers bearing high positive charge densities demonstrated the most effective phage wrapping, as shown by assays for blocking nonspecific binding of the anionic phage coat to a high pI target protein. The results establish the functional group requirements for hybridizing phage with soft materials and solve a major problem in phage display-nonspecific binding by the phage to high pI target proteins.
M13 噬菌体为基于自组装无机和硬材料与噬菌体展示肽相互作用的纳米结构合成提供了支架。此外,噬菌体展示已被用于鉴定与塑料、TiO2 和其他表面的结合物。然而,通过将软材料与噬菌体表面杂交来合成基于噬菌体的材料仍然未被探索。在这里,我们提出了一种有效的“噬菌体包裹”策略,用于简便地合成带有可溶性阳离子聚合物的噬菌体。具有高正电荷密度的聚合物表现出最有效的噬菌体包裹,这可以通过测定噬菌体的阴离子外壳与高 pI 靶蛋白的非特异性结合来证明。结果确定了将噬菌体与软材料杂交的功能基团要求,并解决了噬菌体展示中的一个主要问题,即噬菌体与高 pI 靶蛋白的非特异性结合。