Houseman Benjamin T, Mrksich Milan
Department of Chemistry and The Institute for Biophysical Dynamics, The University of Chicago, Chicago, IL 60637, USA.
Chem Biol. 2002 Apr;9(4):443-54. doi: 10.1016/s1074-5521(02)00124-2.
This paper reports a chemical strategy for preparing carbohydrate arrays and utilizes these arrays for the characterization of carbohydrate-protein interactions. Carbohydrate chips were prepared by the Diels-Alder-mediated immobilization of carbohydrate-cyclopentadiene conjugates to self-assembled monolayers that present benzoquinone and penta(ethylene glycol) groups. Surface plasmon resonance spectroscopy showed that lectins bound specifically to immobilized carbohydrates and that the glycol groups prevented nonspecific protein adsorption. Carbohydrate arrays presenting ten monosaccharides were then evaluated by profiling the binding specificities of several lectins. These arrays were also used to determine the inhibitory concentrations of soluble carbohydrates for lectins and to characterize the substrate specificity of beta-1,4-galactosyltransferase. Finally, a strategy for preparing arrays with carbohydrates generated on solid phase is shown. This surface engineering strategy will permit the preparation and evaluation of carbohydrate arrays that present diverse and complex structures.
本文报道了一种制备碳水化合物阵列的化学策略,并利用这些阵列对碳水化合物 - 蛋白质相互作用进行表征。通过狄尔斯 - 阿尔德介导的碳水化合物 - 环戊二烯共轭物固定到呈现苯醌和五(乙二醇)基团的自组装单分子层上来制备碳水化合物芯片。表面等离子体共振光谱表明凝集素与固定化的碳水化合物特异性结合,并且二醇基团可防止非特异性蛋白质吸附。然后通过分析几种凝集素的结合特异性来评估呈现十种单糖的碳水化合物阵列。这些阵列还用于确定可溶性碳水化合物对凝集素的抑制浓度,并表征β-1,4-半乳糖基转移酶的底物特异性。最后,展示了一种制备在固相上生成碳水化合物的阵列的策略。这种表面工程策略将允许制备和评估呈现多样且复杂结构的碳水化合物阵列。