Department of Chemical and Environmental Engineering, The University of Arizona, Tucson, AZ 85721,USA.
J Chromatogr A. 2012 Mar 2;1227:115-25. doi: 10.1016/j.chroma.2011.12.091. Epub 2012 Jan 8.
Despite the many efforts to develop efficient protein purification techniques, the isolation of peptides and small proteins on a larger than analytical scale remains a significant challenge. Recovery of small biomolecules from diluted complex biological mixtures, such as human serum, employing porous adsorbents is a difficult task mainly due to the presence of concentrated large biomolecules that can add undesired effects in the system such as blocking of adsorbent pores, impairing diffusion of small molecules, or competition for adsorption sites. Adsorption and size exclusion chromatography (AdSEC) controlled access media, using polyethylene glycol (PEG) as a semi-permeable barrier on a polysaccharide matrix, have been developed and explored in this work to overcome such effects and to preferentially adsorb small molecules while rejecting large ones. In the first part of this work, adsorption studies were performed with small peptides and proteins from synthetic mixtures using controlled access polymer permeation adsorption (CAPPA) media created by effectively grafting PEG on an immobilized metal affinity chromatography (IMAC) agarose resin, where chelating agents and immobilized metal ions were used as the primary affinity binding sites. Synthetic mixtures consisted of bovine serum albumin (BSA) with small proteins, peptides, amino acids (such as histidine or Val⁴-Angiotensin III), and small molecules-spiked human serum. The synthesized hybrid adsorbent consisted of agarose beads modified with iminodiacetic (IDA) groups, loaded with immobilized Cu(II) ions, and PEG. These CAPPA media with grafted PEG on the interior and exterior surfaces of the agarose matrix were effective in rejecting high molecular weight proteins. Different PEG grafting densities and PEG of different molecular weight were tested to determine their effect in rejecting and controlling adsorbent permeation properties. Low grafting density of high molecular weight PEG was found to be as effective as high grafting density of low molecular weight PEG in the rejecting properties of the semi-permeable synthesized media.
尽管已经做出了许多努力来开发高效的蛋白质纯化技术,但在大于分析规模上分离肽和小蛋白质仍然是一个重大挑战。使用多孔吸附剂从小分子生物混合物(如人血清)中回收小生物分子是一项艰巨的任务,主要是由于存在浓缩的大生物分子,它们会在系统中产生不良影响,例如堵塞吸附剂孔、阻碍小分子扩散或与吸附位点竞争。本工作中开发并探索了使用聚乙二醇(PEG)作为多糖基质上的半渗透屏障的吸附和尺寸排阻色谱(AdSEC)控制访问介质,以克服这些影响并优先吸附小分子,同时排斥大分子。在这项工作的第一部分中,使用来自合成混合物的小肽和蛋白质进行了吸附研究,该合成混合物使用通过有效接枝聚乙二醇(PEG)在固定化金属亲和色谱(IMAC)琼脂糖树脂上创建的受控访问聚合物渗透吸附(CAPPA)介质进行,其中螯合剂和固定化金属离子被用作主要亲和结合位点。合成混合物由牛血清白蛋白(BSA)与小蛋白质、肽、氨基酸(如组氨酸或 Val⁴-血管紧张素 III)和小分子-缀合人血清组成。合成的混合吸附剂由琼脂糖珠组成,该琼脂糖珠用亚氨基二乙酸(IDA)基团改性,负载固定化的 Cu(II)离子和 PEG。这些在琼脂糖基质的内外表面接枝 PEG 的 CAPPA 介质有效地排斥高分子量蛋白质。测试了不同的 PEG 接枝密度和不同分子量的 PEG,以确定它们在排斥和控制吸附剂渗透性能方面的效果。发现高分子量 PEG 的低接枝密度与低分子量 PEG 的高接枝密度在半渗透合成介质的排斥性能方面同样有效。