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基于亲和力的聚异氰肽生物共轭物纯化

Affinity-Based Purification of Polyisocyanopeptide Bioconjugates.

作者信息

Hammink Roel, Eggermont Loek J, Zisis Themistoklis, Tel Jurjen, Figdor Carl G, Rowan Alan E, Blank Kerstin G

机构信息

Department of Molecular Materials, Institute for Molecules and Materials, Radboud University , Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands.

Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center , Geert Grooteplein 26, 6525 GA Nijmegen, The Netherlands.

出版信息

Bioconjug Chem. 2017 Oct 18;28(10):2560-2568. doi: 10.1021/acs.bioconjchem.7b00398. Epub 2017 Sep 15.

Abstract

Water-soluble polyisocyanopeptides (PICs) are a new class of synthetic polymers that mimic natural protein-based filaments. Their unique semiflexible properties combined with a length of several hundred nanometers have recently enabled a number of biomedical applications ranging from tissue engineering to cancer immunotherapy. One crucial step toward the further development of PICs for these applications is the efficient and controlled synthesis and purification of PIC-biomolecule conjugates. Considering the large size of PICs and the biomolecules to be conjugated, conjugation reactions do usually not proceed to completion due to steric effects. As a consequence, purification of the reaction mixture is necessary to separate the obtained bioconjugates from unreacted biomolecules. As a direct result of the semiflexible nature of PICs, standard polymer and protein purification methods based on molecular weight have not been successful. Here, we introduce a new affinity-based purification method utilizing biotin as an affinity tag. PICs decorated with a controlled and tunable density of biotin molecules (biotinPICs) were efficiently bound to and eluted from a monoavidin resin in buffered aqueous solution. Using these biotinPICs, two different protein conjugates were synthesized, one carrying the enzyme alkaline phosphatase (PhoA) and the other T-cell activating anti-CD3 antibodies. The resulting biotinPIC-protein conjugates were successfully obtained in high purity (>90%) and without any loss of protein activity. The high purity greatly simplifies the analysis of biotinPIC bioconjugates, such as the determination of the average number of biomolecules conjugated per biotinPIC chain. Most importantly, it allows for the direct and straightforward application of the obtained bioconjugates in the desired applications. The new method developed may further be adapted for the purification of other advanced bioconjugates that are difficult to obtain in high purity with the available standard methods.

摘要

水溶性聚异氰酸肽(PICs)是一类新型合成聚合物,可模拟天然蛋白质基细丝。其独特的半柔性特性与数百纳米的长度相结合,最近已实现了从组织工程到癌症免疫疗法等多种生物医学应用。对于这些应用而言,PICs进一步发展的关键一步是高效且可控地合成和纯化PIC-生物分子缀合物。考虑到PICs和待缀合生物分子的尺寸较大,由于空间效应,缀合反应通常无法进行到底。因此,需要对反应混合物进行纯化,以从未反应的生物分子中分离出所得的生物缀合物。由于PICs具有半柔性的本质,基于分子量的标准聚合物和蛋白质纯化方法并不成功。在此,我们引入一种新的基于亲和作用的纯化方法,利用生物素作为亲和标签。用可控且可调密度的生物素分子修饰的PICs(生物素化PICs)在缓冲水溶液中能有效地与单抗生物素蛋白树脂结合并从其上洗脱。使用这些生物素化PICs,合成了两种不同的蛋白质缀合物,一种携带碱性磷酸酶(PhoA),另一种携带激活T细胞的抗CD3抗体。所得的生物素化PIC-蛋白质缀合物成功以高纯度(>90%)获得,且蛋白质活性无任何损失。高纯度极大地简化了生物素化PIC生物缀合物的分析,例如测定每个生物素化PIC链缀合的生物分子平均数。最重要的是,它允许将所得的生物缀合物直接且简便地应用于所需应用中。所开发的新方法可能进一步适用于纯化其他难以用现有标准方法获得高纯度的先进生物缀合物。

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