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使用放射性抑制剂配体结合法测定人血清中的血管紧张素转换酶(ACE)

Angiotensin-converting enzyme (ACE) measurement in human serum using radioinhibitor ligand binding.

作者信息

Jackson B, Cubela R, Johnston C I

出版信息

Aust J Exp Biol Med Sci. 1986 Apr;64 ( Pt 2):149-55. doi: 10.1038/icb.1986.16.

Abstract

MK351A, a tyrosyl analogue of enalaprilic acid (MK422) is a potent inhibitor of angiotensin-converting enzyme (ACE). MK351A was radioiodinated with 125I and used to develop a radio inhibitor binding assay for human serum ACE. 125I MK351A associated rapidly and reversibly with human serum ACE (T 1/2 = 1/2 h). Bound 125I MK351A was displaced by an excess of cold MK351A, to give non-specific binding of less than 1%. Scatchard analysis of binding was linear (r = -0.99, n = 6, p less than 0.001), indicating a single class of binding site. ACE was estimated in serum from normal patients and patients with sarcoid by the radio inhibitor binding assay and by enzyme kinetic assay using Hip-His-Leu as substrate. The two methods for ACE estimation correlated closely (r = 0.87, n = 82, p less than 0.001). The radio inhibitor binding assay for human serum ACE is a simple, sensitive and specific assay which utilizes novel assay methodology.

摘要

MK351A是依那普利酸(MK422)的酪氨酸类似物,是一种有效的血管紧张素转换酶(ACE)抑制剂。MK351A用125I进行放射性碘化,并用于开发一种针对人血清ACE的放射性抑制剂结合测定法。125I MK351A与人血清ACE迅速且可逆地结合(半衰期=1/2小时)。过量的冷MK351A可取代结合的125I MK351A,使非特异性结合小于1%。结合的Scatchard分析呈线性(r=-0.99,n=6,p<0.001),表明存在单一类别的结合位点。通过放射性抑制剂结合测定法以及使用Hip-His-Leu作为底物的酶动力学测定法,对正常患者和结节病患者的血清中的ACE进行了估计。两种ACE估计方法密切相关(r=0.87,n=82,p<0.001)。用于人血清ACE的放射性抑制剂结合测定法是一种利用新型测定方法的简单、灵敏且特异的测定法。

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