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蛋白质-聚合物在可逆固定化载体上的固相合成。

Solid-phase synthesis of protein-polymers on reversible immobilization supports.

机构信息

Center for Polymer-Based Protein Engineering, Carnegie Mellon University, 5000 Forbes Avenue, Pittsburgh, PA, 15213, USA.

Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, PA, 15213, USA.

出版信息

Nat Commun. 2018 Feb 27;9(1):845. doi: 10.1038/s41467-018-03153-8.

Abstract

Facile automated biomacromolecule synthesis is at the heart of blending synthetic and biologic worlds. Full access to abiotic/biotic synthetic diversity first occurred when chemistry was developed to grow nucleic acids and peptides from reversibly immobilized precursors. Protein-polymer conjugates, however, have always been synthesized in solution in multi-step, multi-day processes that couple innovative chemistry with challenging purification. Here we report the generation of protein-polymer hybrids synthesized by protein-ATRP on reversible immobilization supports (PARIS). We utilized modified agarose beads to covalently and reversibly couple to proteins in amino-specific reactions. We then modified reversibly immobilized proteins with protein-reactive ATRP initiators and, after ATRP, we released and analyzed the protein polymers. The activity and stability of PARIS-synthesized and solution-synthesized conjugates demonstrated that PARIS was an effective, rapid, and simple method to generate protein-polymer conjugates. Automation of PARIS significantly reduced synthesis/purification timelines, thereby opening a path to changing how to generate protein-polymer conjugates.

摘要

将生物大分子进行自动化合成是融合合成生物学和生物技术的核心。当化学发展到可以从可反复固定的前体中合成核酸和肽时,我们才第一次完全获得了非生物/生物合成的多样性。然而,蛋白质-聚合物缀合物的合成一直以来都是在溶液中进行的,需要多步、多天的反应,这些反应将创新的化学与具有挑战性的纯化技术相结合。在这里,我们报告了在可逆固定化载体(PARIS)上通过蛋白质原子转移自由基聚合(protein-ATRP)生成蛋白质-聚合物杂化物的方法。我们利用修饰后的琼脂糖珠在氨基特异性反应中与蛋白质进行共价且可反复的连接。然后,我们用蛋白质反应性 ATRP 引发剂修饰可逆固定化的蛋白质,ATRP 之后,我们释放并分析了蛋白质聚合物。PARIS 合成和溶液合成的缀合物的活性和稳定性表明,PARIS 是一种有效、快速和简单的生成蛋白质-聚合物缀合物的方法。PARIS 的自动化大大缩短了合成/纯化的时间线,从而为改变如何生成蛋白质-聚合物缀合物开辟了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2540/5829226/96d4e27f27e1/41467_2018_3153_Fig1_HTML.jpg

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