A NONISOTOPIC IMMUNOASSAY FOR GUANOSINE 3'5'-CYCLIC MONOPHOSPHATE USING A CYCLIC GMP-BIOTIN CONJUGATE AS TRACER

被引:10
作者
DRESSENDORFER, RA [1 ]
HEIM, JM [1 ]
GERZER, R [1 ]
STRASBURGER, CJ [1 ]
机构
[1] DEUTSCH FORSCH ANSTALT LUFT & RAUMFAHRT,INST AEROSP MED,D-51140 COLOGNE,GERMANY
来源
JOURNAL OF IMMUNOASSAY | 1995年 / 16卷 / 01期
关键词
CGMP; LABELING PROCEDURES; NON ISOTOPIC IMMUNOASSAYS;
D O I
10.1080/15321819508013548
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
2'-O-monosuccinylguanosine 3':5'-cyclic monophosphate was coupled to N-biotinyl-1,8-diamino-3,6-dioxaoctane after converting succinyl-cGMP into its N-hydroxysuccinimide active ester. Isolation and purification of the succinyl-cGMP-biotin conjugate was performed with FPLC(R) using reversed phase chromatography. The synthesis described yielded a conjugate suitable for use as tracer in immunoassays for the cGMP measurement in plasma and urine samples. Employing biotin as the primary probe in a competitive solid phase immunoassay allows for flexible end point determination by means of commercially available labeled streptavidin derivatives. Streptavidin-europium was used in conjunction with the DELFIA(R)-system for time-resolved fluorometric end point measurement (TR-FIA), streptavidin-horseradish peroxidase was used for colorimetric end point determination (EIA). Both non radioactive immunoassay systems showed excellent correlation with the reference radioimmunoassay, good sensitivity and reproducibility. The succinyl-cGMP-biotin conjugate was shown to be stable for more than two years without any apparent loss of chemical stability or immunological reactivity.
引用
收藏
页码:37 / 53
页数:17
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