Kilian Kristopher A, Lai Leo M H, Magenau Astrid, Cartland Siân, Böcking Till, Di Girolamo Nick, Gal Michael, Gaus Katharina, Gooding J Justin
School of Chemistry, University of New South Wales, Sydney, New South Wales 2052, Australia.
Nano Lett. 2009 May;9(5):2021-5. doi: 10.1021/nl900283j.
Monitoring enzyme secretion in tissue culture has proved challenging because to date the activity cannot be continuously measured in situ. In this Letter, we present a solution using biopolymer loaded photonic crystals of anodized silicon. Shifts in the optical response by proteolytic degradation of the biopolymer provide label-free sensing with unprecedented low detection limits (1 pg) and calculation of kinetic parameters. The enhancement in sensitivity relative to previous photonic crystal sensors constitutes a change in the sensing paradigm because here the entire pore space is responsive to the secreted enzyme rather than just the pore walls. In situ monitoring is demonstrated by detecting secretion of matrix metalloprotease 9 from stimulated human macrophages.
在组织培养中监测酶分泌已被证明具有挑战性,因为迄今为止,无法在原位连续测量其活性。在本信函中,我们提出了一种使用负载生物聚合物的阳极氧化硅光子晶体的解决方案。生物聚合物的蛋白水解降解引起的光学响应变化提供了具有前所未有的低检测限(1皮克)的无标记传感以及动力学参数的计算。相对于以前的光子晶体传感器,灵敏度的提高构成了传感范式的转变,因为在这里,整个孔隙空间对分泌的酶有反应,而不仅仅是孔壁。通过检测受刺激的人类巨噬细胞分泌的基质金属蛋白酶9,证明了原位监测。