Graduate School of Environmental Studies, Tohoku University, 6-6-11, Aramaki, Aoba, Sendai 980-8579, Japan.
Biotechnol Bioeng. 2012 Aug;109(8):2163-7. doi: 10.1002/bit.24461. Epub 2012 Feb 22.
A new electrochemical assay for the detection of secreted alkaline phosphatase (SEAP) from transfectant HeLa cells is proposed using a microarray device and scanning electrochemical microscopy (SECM). The assay consists of two steps: the first is the incubation of a transfected cell in a microarray culture device covered with a substrate modified with anti-SEAP under physiological conditions without any additives. The array device consists of a 4 × 4 array of microwells having a size of 100 µm × 100 µm (diameter × depth). The second step is SECM measurement of secreted SEAP at the antibody-immobilized substrate. This assay ensures accuracy and intactness because the undesired influence of endogeneous ALP is eliminated and the transfected cells are incubated in a culture device under suitable conditions. We successfully detected the expression of SEAP from intact cells at the single-cell level using this assay. The system is useful as a cell-based gene-expression assay.
提出了一种使用微阵列装置和扫描电化学显微镜(SECM)检测转染 HeLa 细胞分泌碱性磷酸酶(SEAP)的新电化学分析方法。该测定法包括两个步骤:第一步是在微阵列培养装置中在没有任何添加剂的情况下在覆盖有经抗-SEAP 修饰的底物的条件下孵育转染细胞。阵列装置由具有 100 µm×100 µm(直径×深度)尺寸的 4×4 个微孔阵列组成。第二步是在抗体固定化的基质上进行 SECM 测量分泌的 SEAP。由于消除了内源性 ALP 的不良影响,并且转染细胞在合适的条件下在培养装置中孵育,因此该测定法确保了准确性和完整性。我们使用该测定法成功地在单细胞水平上检测到完整细胞中 SEAP 的表达。该系统可用作基于细胞的基因表达测定法。