Department of Chemical Engineering and Biotechnology Process Engineering Center, Massachusetts Institute of Technology, Room 56-469, Cambridge, MA, USA.
Cytotechnology. 2000 Nov;34(3):237-42. doi: 10.1023/A:1008170023099.
A flow injection analysis (FIA) system is presented for a twostep immunoassay-based determination of the total humanprolactin (hPRL) concentration along with its degree ofglycosylation. Separate measurement of total hPRL and nonglysosylated human prolactin (nG-hPRL) were made using twoflow-through cartridges each containing immobilized antibodiesof different specificity. The antibodies are immobilized on thesurface of a carrier. Glycosylated hPRL (G-hPRL) and, thus, thedegree of glycosylation were calculated by the differencebetween the two specific determinations. Enhanced specificityfor the determination of nG-hPRL was obtained using unfavorablebinding conditions through incorporation of alkaline pH andchaotropic agents into the carrier/dispersion buffer. The assayfor total hPRL and nG-hPRL were each found to be linear withinthe relevant concentration range. The results of the two-stepFIA method were found to agree with those obtained by thestandard methods of ELISA and western blotting while offeringthe advantage of minimal analysis time (10 min) and eliminationof manual manipulations.
一种基于流动注射分析(FIA)的两步免疫分析法系统,用于同时测定总人催乳素(hPRL)浓度及其糖基化程度。总 hPRL 和非糖基化人催乳素(nG-hPRL)的单独测定是使用两个包含不同特异性固定化抗体的流通式试剂盒完成的。抗体固定在载体的表面。通过在载体/分散缓冲液中加入碱性 pH 值和离液剂,使糖基化 hPRL(G-hPRL)和糖基化程度通过两种特异性测定的差异计算得出。通过采用不利的结合条件,将碱性 pH 值和离液剂纳入载体/分散缓冲液中,可获得对 nG-hPRL 测定的增强特异性。总 hPRL 和 nG-hPRL 的测定均在相关浓度范围内呈线性关系。两步 FIA 法的结果与 ELISA 和 Western blot 等标准方法的结果一致,同时具有分析时间最短(10 分钟)和消除手动操作的优点。