Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA 20110, USA.
Curr Mol Med. 2010 Mar;10(2):133-41. doi: 10.2174/156652410790963268.
Clinically relevant biomarkers exist in blood and body fluids in extremely low concentrations, are masked by high abundance high molecular weight proteins, and often undergo degradation during collection and transport due to endogenous and exogenous proteinases. Nanoparticles composed of a N-isopropylacrylamide hydrogel core shell functionalized with internal affinity baits are a new technology that can address all of these critical analytical challenges for disease biomarker discovery and measurement. Core-shell, bait containing, nanoparticles can perform four functions in one step, in solution, in complex biologic fluids (e.g. blood or urine): a) molecular size sieving, b) complete exclusion of high abundance unwanted proteins, c) target analyte affinity sequestration, and d) complete protection of captured analytes from degradation. Targeted classes of protein analytes sequestered by the particles can be concentrated in small volumes to effectively amplify (up to 100 fold or greater depending on the starting sample volume) the sensitivity of mass spectrometry, western blotting, and immunoassays. The materials utilized for the manufacture of the particles are economical, stable overtime, and remain fully soluble in body fluids to achieve virtually 100 percent capture of all solution phase target proteins within a few minutes.
临床上相关的生物标志物存在于血液和体液中,浓度极低,被高丰度的高分子量蛋白质所掩盖,并且由于内源性和外源性蛋白酶,在采集和运输过程中经常发生降解。由 N-异丙基丙烯酰胺水凝胶核壳组成的纳米粒子,其表面功能化有内部亲和诱饵,是一种新技术,可以解决疾病生物标志物发现和测量中所有这些关键分析挑战。核壳型、含有诱饵的纳米粒子可以在一个步骤中完成四个功能,在溶液中,在复杂的生物流体(例如血液或尿液)中:a)分子大小筛分,b)完全排除高丰度不需要的蛋白质,c)目标分析物的亲和捕获,以及 d)完全保护捕获的分析物免受降解。通过粒子捕获的目标蛋白分析物类别可以在小体积中浓缩,以有效地放大(根据起始样品体积,最大可达 100 倍或更高)质谱、western blot 和免疫分析的灵敏度。用于制造粒子的材料经济实惠,随着时间的推移稳定,并且在体液中完全溶解,可在几分钟内几乎 100%捕获所有溶液相靶蛋白。