Bai Haihong, Fan Chao, Zhang Wanjun, Pan Yiting, Ma Lin, Ying Wantao, Wang Jianhua, Deng Yulin, Qian Xiaohong, Qin Weijie
National Center for Protein Sciences Beijing , State Key Laboratory of Proteomics , Beijing Proteome Research Center , Tianjin Baodi Hospital , Beijing Institute of Radiation Medicine , China . Email:
School of Life Science and Technology , Beijing Institute of Technology , Beijing , China.
Chem Sci. 2015 Jul 1;6(7):4234-4241. doi: 10.1039/c5sc00396b. Epub 2015 May 26.
Liquid phase homogeneous reactions using soluble polymer supports have found numerous applications in homogeneous catalysis and organic synthesis because of their advantages of no interface mass transfer limitation and a high conversion rate. However, their application in analytical separation is limited by the inefficient/inconvenient recovery of the target molecules from the extremely complex biological samples. Here, we report a stimuli-responsive polymer system for facile and efficient enrichment of trace amounts of biomolecules from complex biological samples. The soluble polymer supports provide a homogeneous reaction system with fast mass transfer and facilitate interactions between the supports and the target molecules. More importantly, the stimuli-responsive polymers exhibit reversible self-assembly and phase separation under pH variations, which leads to facial sample recovery with a high yield of the target biomolecules. The stimuli-responsive polymer is successfully applied to the enrichment of low abundant -glycoproteins/glycopeptides, which play crucial roles in various key biological processes in mammals and are closely correlated with the occurrence, progression and metastasis of cancer. -Glycoprotein is coupled to the stimuli-responsive polymer using the reported hydrazide chemistry with pre-oxidation of the oligosaccharide structure. Highly efficient enrichment of -glycoproteins/-glycopeptides with >95% conversion rate is achieved within 1 h, which is eight times faster than using solid/insoluble hydrazide enrichment materials. Mass spectrometry analysis achieves low femtomolar identification sensitivity and obtained 1317 -glycopeptides corresponding to 458 -glycoproteins in mouse brain, which is more than twice the amount obtained after enrichment using commercial solid/insoluble materials. These results demonstrate the capability of this "smart" polymer system to combine stimuli-responsive and target-enrichment moieties to achieve improved identification of key biological and disease related biomolecules.
由于不存在界面传质限制和高转化率的优点,使用可溶性聚合物载体的液相机均相反应在均相催化和有机合成中已得到广泛应用。然而,它们在分析分离中的应用受到从极其复杂的生物样品中回收目标分子效率低下/不便的限制。在此,我们报道了一种刺激响应聚合物体系,用于从复杂生物样品中简便高效地富集痕量生物分子。可溶性聚合物载体提供了一个传质快速的均相反应体系,并促进了载体与目标分子之间的相互作用。更重要的是,刺激响应聚合物在pH变化下表现出可逆的自组装和相分离,这使得能够简便地回收样品,且目标生物分子的产率很高。该刺激响应聚合物已成功应用于低丰度糖蛋白/糖肽的富集,这些糖蛋白/糖肽在哺乳动物的各种关键生物过程中起着至关重要的作用,并且与癌症的发生、发展和转移密切相关。利用报道的酰肼化学方法并对寡糖结构进行预氧化,将糖蛋白偶联到刺激响应聚合物上。在1小时内实现了转化率>95%的高效糖蛋白/糖肽富集,这比使用固体/不溶性酰肼富集材料快八倍。质谱分析实现了低飞摩尔级别的鉴定灵敏度,并在小鼠脑中获得了对应于458种糖蛋白的1317种糖肽,这比使用商业固体/不溶性材料富集后获得的数量多两倍以上。这些结果证明了这种“智能”聚合物体系能够结合刺激响应和目标富集部分,以实现对关键生物和疾病相关生物分子的改进鉴定。