Pazhanisamy S, Stuver C M, Livingston D J
Vertex Pharmaceuticals Incorporated, Cambridge, Massachusetts 02139, USA.
Anal Biochem. 1995 Jul 20;229(1):48-53. doi: 10.1006/abio.1995.1377.
Enzyme-based assays are commonly employed in clinical and pharmaceutical laboratories to aid in quantitation of organic substances. Many enzyme assays are tedious, requiring the addition of reagents at multiple time intervals. The HPLC-based analysis of reaction products requires an additional step of vialing the samples and placing them in the autosampler. Such time-consuming, repetitive procedures are ideally suited for automation. We automated an HIV protease assay for the purposes of screening compounds as inhibitors of HIV protease and determining inhibition constants. Automation was accomplished by interfacing a robotic sample processor from a Gilson Model 232/401 biocompatible automatic sample processor and injector, with a Hewlett Packard HPLC. We used this configuration to automate the following steps: (a) preparation of serial dilutions of inhibitor, (b) enzyme assay setup, and (c) quantitation of products of enzyme assays. The resulting automated method produced inhibition constants that were of comparable accuracy and precision to those determined by manual methods.
基于酶的分析方法常用于临床和制药实验室,以辅助定量有机物质。许多酶分析很繁琐,需要在多个时间间隔添加试剂。基于高效液相色谱(HPLC)对反应产物的分析需要额外的步骤,即将样品装入小瓶并放入自动进样器中。这种耗时、重复的程序非常适合自动化操作。为了筛选作为HIV蛋白酶抑制剂的化合物并确定抑制常数,我们对HIV蛋白酶分析进行了自动化操作。通过将吉尔森232/401型生物相容性自动样品处理器和进样器中的机器人样品处理器与惠普HPLC连接来实现自动化。我们使用这种配置对以下步骤进行自动化:(a)抑制剂系列稀释液的制备,(b)酶分析设置,以及(c)酶分析产物的定量。由此产生的自动化方法所得到的抑制常数在准确性和精密度方面与手动方法测定的结果相当。