1984
DOI: 10.1093/clinchem/30.6.901
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Automated kinetic determination of angiotensin-converting enzyme in serum.

Abstract: In this automated kinetic modification of a previous method (Anal Biochem 95: 540-548, 1979) for determining angiotensin-converting enzyme (EC 3.4.15.1), 3-(2- furylacryloyl )-L- phenylalanylglycylglycine is used as the substrate. The change in absorbance at 340 nm is used to monitor hydrolysis of the substrate. The rate of hydrolysis is roughly threefold greater than with previously reported substrates, so assay time and sensitivity are improved.

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Cited by 26 publications
(4 citation statements)
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“…ACE extract (10 μl) was added to the mixture and the absorbance at 340 nm was measured using an ELISA reader Expert 96 (ASYS Hi-tech, Eugendorf, Austria) over a period of 25 min at 37°C. For determination of the IC 50 value for ACE-inhibitory activity of each peptide fraction, the activity of ACE in units/l was calculated according to the following formula (Harjanne 1984):where V t is the final assay volume; V s is the volume of ACE present in the assay; d is the light path (cm); Δε is the absorbance change at 340 nm obtained by the complete hydrolysis of 1 m m of FAPGG to FAP and GG and ΔA/min is the decrease in absorbance at 340 nm per minute. The IC 50 value was determined from a plot of percentage of ACE inhibitory activity against the peptide concentration.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…ACE extract (10 μl) was added to the mixture and the absorbance at 340 nm was measured using an ELISA reader Expert 96 (ASYS Hi-tech, Eugendorf, Austria) over a period of 25 min at 37°C. For determination of the IC 50 value for ACE-inhibitory activity of each peptide fraction, the activity of ACE in units/l was calculated according to the following formula (Harjanne 1984):where V t is the final assay volume; V s is the volume of ACE present in the assay; d is the light path (cm); Δε is the absorbance change at 340 nm obtained by the complete hydrolysis of 1 m m of FAPGG to FAP and GG and ΔA/min is the decrease in absorbance at 340 nm per minute. The IC 50 value was determined from a plot of percentage of ACE inhibitory activity against the peptide concentration.…”
Section: Methodsmentioning
confidence: 99%
“…ACE extract (10 μl) was added to the mixture and the absorbance at 340 nm was measured using an ELISA reader Expert 96 (ASYS Hi-tech, Eugendorf, Austria) over a period of 25 min at 37°C. For determination of the IC 50 value for ACE-inhibitory activity of each peptide fraction, the activity of ACE in units/l was calculated according to the following formula (Harjanne 1984):…”
Section: Determination Of the Ace-inhibitory Activitymentioning
confidence: 99%
“…ACE activity assays were made at 340 nm and 37°C using a measuring time of 10 min. One unit (U) of ACE activity was expressed as the amount of the enzyme that will hydrolyze 1 µmol of the substrate FAPGG into FAP and glycyl-glycine in 1 min at 37°C ( 14 ). Normalized plasma ACE activity was determined at the end of the measurements, by dividing the ACE value to total plasma protein value for each animal.…”
Section: Methodsmentioning
confidence: 99%
“…(FAPGG) (Sigma Diagnostic-305, St Louis, MO, USA) was used as a substrate according to the method described by Harjanne (16). Three determinations were performed from each serum sample and the mean result was chosen as the final value.…”
Section: Furiulacr Yloil-l-phenyl-alanil-glicilglicinementioning
confidence: 99%