Strong R A, Cho B Y, Fisher D H, Nappier J, Krull I S
Department of Chemistry, Northeastern University, Boston, MA 02115, USA.
Biomed Chromatogr. 1996 Nov-Dec;10(6):337-45. doi: 10.1002/(SICI)1099-0801(199611)10:6<337::AID-BMC627>3.0.CO;2-O.
An indirect detection method using high-performance immunoaffinity chromatography (HPIAC) was used to measure low levels of an analogue of bovine Growth Hormone Releasing Factor (bGHRF). An antibody (Ab) labelled with alkaline phosphate (ALP) was incubated with the bGHRF analogue to perform a complex between the antigen (Ag) and the antibody-enzyme (Ab-En) conjugate. The complex was then injected onto a cartridge containing an immobilized Ag affinity support. Species which were not recognized by the affinity cartridge, i.e. eluted, were then directly combined, via a connecting tee, with a buffer containing a substrate. Incubation proceeded on-line, inside a knitted reactor coil, under conditions of constant flow. The subsequent generation of a fluorescently active substrate product was detected by conventional means. The assay described has a linear response region from 1.0 to 25 ng of the bGHRF analogue and a limit of detection of 0.60 ng (1.7 x 10(2) femtomole, 30 p.p.b.). This approach was compared against a method in the antigen/Ab-En complex was injected onto a immobilized Ab affinity cartridge to form an antibody-antigen conjugate sandwich and subsequent stop-flow incubation with substrate.
采用一种使用高效免疫亲和色谱法(HPIAC)的间接检测方法来测量低水平的牛生长激素释放因子类似物(bGHRF)。将用碱性磷酸酶(ALP)标记的抗体(Ab)与bGHRF类似物孵育,以形成抗原(Ag)与抗体 - 酶(Ab - En)缀合物之间的复合物。然后将该复合物注入装有固定化Ag亲和支持物的柱中。未被亲和柱识别的物质(即被洗脱)随后通过连接三通直接与含有底物的缓冲液混合。在编织的反应盘管内,在恒定流速条件下进行在线孵育。通过常规方法检测随后产生的具有荧光活性的底物产物。所述测定法对bGHRF类似物的线性响应范围为1.0至25 ng,检测限为0.60 ng(1.7×10²飞摩尔,30 ppb)。将该方法与另一种方法进行比较,在后一种方法中,将抗原/Ab - En复合物注入固定化Ab亲和柱中以形成抗体 - 抗原缀合物夹心,随后与底物进行停流孵育。