Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1600, United States.
Biomacromolecules. 2010 Dec 13;11(12):3668-72. doi: 10.1021/bm101123k. Epub 2010 Nov 3.
We describe the application of flash column chromatography on silica gel as a rapid and general method to obtain pure α-amino acid-N-carboxyanhydride (NCA) monomers, the widely used precursors for the synthesis of polypeptides, without the need for recrystallization. This technique was effective at removing all common impurities from NCAs and was found to work for a variety of NCAs, including those synthesized using different routes, as well as those bearing either hydrophilic or hydrophobic side chains. All chromatographed NCAs required no further purification and could be used directly to form high molecular weight polypeptides. This procedure is especially useful for the preparation of highly functional and low melting NCAs that are difficult to crystallize and, consequently, to polymerize. This method solves many long-standing problems in NCA purification and provides rapid access to NCAs that were previously inaccessible in satisfactory quality for controlled polymerization. This method is also practical in that it requires less time than recrystallization and often gives NCAs in improved yields.
我们描述了一种在硅胶上进行快速柱层析的方法,该方法可用于快速且普遍地获得纯净的α-氨基酸-N-羧酸酐(NCA)单体,这是合成多肽的常用前体,而无需进行重结晶。该技术可有效去除 NCA 中的所有常见杂质,并且适用于多种 NCA,包括使用不同路线合成的 NCA 以及具有亲水或疏水侧链的 NCA。所有经层析分离的 NCA 无需进一步纯化,可直接用于形成高分子量多肽。对于制备难以结晶且难以聚合的高功能低熔点 NCA 而言,该方法尤其有用。该方法解决了 NCA 纯化方面的许多长期存在的问题,为以前无法以令人满意的质量获得的用于可控聚合的 NCA 提供了快速途径。该方法在时间上也比重结晶更短,并且通常可以提高 NCA 的产率。