School of Chemistry, Australian Centre for NanoMedicine and the ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, The University of New South Wales, Sydney 2052, Australia; School of Physics, The University of New South Wales, Sydney 2052, Australia.
School of Chemistry, Australian Centre for NanoMedicine and the ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, The University of New South Wales, Sydney 2052, Australia.
Biosens Bioelectron. 2019 Feb 15;127:229-235. doi: 10.1016/j.bios.2018.12.001. Epub 2018 Dec 7.
The work presented here describes the development of an optical label-free biosensor based on a porous silicon (PSi) Bragg reflector to study heterogeneity in single cells. Photolithographic patterning of a poly(ethylene glycol) (PEG) hydrogel with a photoinitiator was employed on RGD peptide-modified PSi to create micropatterns with cell adhesive and cell repellent areas. Macrophage J774 cells were incubated to form cell microarrays and single cell arrays. Moreover, cells on the microarrays were lysed osmotically with Milli-Q™ water and the infiltration of cell lysate into the porous matrix was monitored by measuring the red shift in the reflectivity. On average, the magnitude of red shift increased with the increase in the number of cells on the micropatterns. The red shift from the spots with single cells varied from spot to spot emphasizing the heterogeneous nature of the individual cells.
本文介绍了一种基于多孔硅(PSi)布拉格反射器的无标记光学生物传感器的开发,用于研究单细胞异质性。在 RGD 肽修饰的 PSi 上使用带有光引发剂的聚(乙二醇)(PEG)水凝胶进行光光刻图案化,以创建具有细胞黏附区和细胞排斥区的微图案。孵育巨噬细胞 J774 细胞以形成细胞微阵列和单细胞阵列。此外,用 Milli-Q™水对微阵列上的细胞进行渗透压裂解,并通过测量反射率的红移来监测细胞裂解物渗透到多孔基质中。平均而言,红移的幅度随微图案上细胞数量的增加而增加。来自单细胞点的红移值因点而异,强调了单个细胞的异质性。