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血管紧张素I的酶免疫测定

Enzyme immunoassay of angiotensin I.

作者信息

Aikawa T, Suzuki S, Murayama M, Hashiba K, Kitagawa T, Ishikawa E

出版信息

Endocrinology. 1979 Jul;105(1):1-6. doi: 10.1210/endo-105-1-1.

Abstract

A very sensitive and specific enzyme immunoassay has been developed for angiotensin I. Angiotensin I was coupled to beta-D-galactosidase by a novel cross-linking reagent, N-(meta-maleimidobenzoyloxy)succinimide. No decrease in the enzyme activity was observed during the coupling procedure. In the angiotensin I-beta-D-galactosidase conjugate, 0.39 mol immunoreactive angiotensin I/mol enzyme were present. A competitive assay with the enzyme-labeled angiotensin I was performed. Antibody-bound and free labeled antigen were separated from each other by the second antibody method, and the enzyme activity of the former was estimated. Using this assay, angiotensin I could be detected in the range of 1.2--50 pg. The sensitivity was 4.5-fold higher than that of the usual RIA. This assay distinguished clearly angiotensin I from angiotensin II, angiotensin III, and (Sar1, Ile8)-angiotensin II. The present method was applied to measure PRA in dogs; the results correlated fairly well with those obtained by the RIA (r = 0.94).

摘要

已开发出一种用于检测血管紧张素I的高灵敏度和特异性的酶免疫测定法。血管紧张素I通过一种新型交联试剂N-(间马来酰亚胺苯甲酰氧基)琥珀酰亚胺与β-D-半乳糖苷酶偶联。在偶联过程中未观察到酶活性降低。在血管紧张素I-β-D-半乳糖苷酶偶联物中,每摩尔酶含有0.39摩尔免疫反应性血管紧张素I。采用酶标记血管紧张素I进行竞争测定。通过第二抗体法将结合抗体的和游离的标记抗原彼此分离,并测定前者的酶活性。利用该测定法,可在1.2-50 pg范围内检测到血管紧张素I。其灵敏度比常规放射免疫测定法高4.5倍。该测定法能清晰地区分血管紧张素I与血管紧张素II、血管紧张素III以及(Sar1, Ile8)-血管紧张素II。本方法应用于测定犬的血浆肾素活性;结果与放射免疫测定法所得结果相当吻合(r = 0.94)。

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