Wibowo Arif, Peters Eric C, Hsieh-Wilson Linda C
Division of Chemistry and Chemical Engineering, California Institute of Technology and Howard Hughes Medical Institute , 1200 East California Boulevard, Pasadena, California 91125, United States.
J Am Chem Soc. 2014 Jul 9;136(27):9528-31. doi: 10.1021/ja502482a. Epub 2014 Jun 25.
Although fucose-α(1-2)-galactose (Fucα(1-2)Gal)-containing glycans have been implicated in cognitive processes such as learning and memory, their precise molecular mechanisms are poorly understood. Here we employed the use of multivalent glycopolymers to enable the first proteome-wide identification of weak affinity, low abundance Fucα(1-2)Gal glycan-binding proteins (GBPs). Biotin-terminated glycopolymers containing photoactivatable cross-linking groups were designed to capture and enrich GBPs from rat brain lysates. Candidate proteins were tested for their ability to bind Fucα(1-2)Gal, and the functional significance of the interaction was investigated for the synaptic vesicle protein SV2a using a knockout mouse system. The results suggest a role for SV2a-Fucα(1-2)Gal interactions in SV2a trafficking and synaptic vesicle recycling. More broadly, our studies outline a general chemical approach for the systems-level discovery of novel GBPs.
尽管含有岩藻糖-α(1-2)-半乳糖(Fucα(1-2)Gal)的聚糖已被认为与学习和记忆等认知过程有关,但其确切的分子机制仍知之甚少。在这里,我们使用多价糖聚合物首次在全蛋白质组范围内鉴定出具有弱亲和力、低丰度的Fucα(1-2)Gal聚糖结合蛋白(GBP)。设计了含有光活化交联基团的生物素末端糖聚合物,用于从大鼠脑裂解物中捕获和富集GBP。测试候选蛋白结合Fucα(1-2)Gal的能力,并使用基因敲除小鼠系统研究了与突触小泡蛋白SV2a相互作用的功能意义。结果表明,SV2a-Fucα(1-2)Gal相互作用在SV2a运输和突触小泡循环中发挥作用。更广泛地说,我们的研究概述了一种用于系统水平发现新型GBP的通用化学方法。