EC 3.4.15.1

Two isozymes of ACE are present in mammals: somatic ACE and testis ACE. Somatic ACE possesses two catalytic domains (N- and C-domains) and a C-terminal transmembrane segment (stalk). Both catalytic domains are zinc-metallopeptidase with the active motif HEMGH where the two histidine residues coordinate the zinc ion. The Km for Hip-His-Leu is 2.51mM. The stalk anchors the enzyme on the membrane and is suspectible to be cleaved by shedding enzymes, resulting in plasma ACE activity. ACE2 is a chimera protein with a single catalytic domain of ACE, and a C-terminal that highly resembles collectrin, which may act as a chaperone protein to deliver other proteins to the brush border membrane. Somatic and testis ACEs in humans contain 1306 and 665 aa residues, respectively. The testis ACE only possesses one catalytic domain.

The ACE and ACE2 genes are located at chromosomes 17q23 and Xp22 in humans, respectively. The testis ACE is transcribed from the same gene with an alternative transcription starting site on the 13th intron of ACE, resulting in only a C-domain and a stalk segment with a unique additional 67 aa N-terminal sequence in humans. The two catalytic domains are the result of gene/domain duplication. The duplication occurred multiple times in evolution as the cnidarians, crustaceans, insects, and vertebrates possess ACE-like enzymes with one or two catalytic domains. No expression studies so far have been performed for nonmammalian ACE and ACE2. 

The expression of ACE is affected by steroids and the thyroid hormone, but the details of the regulation are not clear. ACE is under promoter regulation by hypoxiainducing factor 1α (HIF-1α), which upregulates the ACE expression under hypoxic conditions, resulting in an increase in Ang II concentration. Under hypoxia, ACE2 will be downregulated; it was shown that it is indirectly controlled by Ang II, but not HIF-1α.  Testis ACE expression control is highly specific and regulated by a tissue-specific promoter located immediately -59 bp of the transcription start site, which is frequently used in testis-specific overexpression studies. Hypoxia induced by high temperature decreased the gill ACE activity but had no effect on the kidney in the carp. Promoters of ACE2 from mammals, amphibians, and teleosts drive specific expression in the heart. Cis-Element search results discovered WGATAR motifs in all putative ACE2 promoters from different vertebrates, suggesting a possible role of GATA family transcriptional factors in ACE2 expression regulation.

The first ACE inhibitor was a peptide antagonist called SQ 20,881 (GWPRPEIPP); it was discovered from snake venom but was not orally active. The snake venom peptides were further studied to produce the first orally active form, captopril, which lowers the blood pressure of essential hypertensive patients. The most common side effects of captopril are a cough, skin rash, and loss of taste. Therefore, derivatives such as enalapril, lisinopril, and ramipril were developed with fewer side effects. After the discovery of the N- and C-domains of ACE, specific domain inhibitors were developed to increase specificity. Ang I is mainly hydrolyzed by the C-domain in vivo, but BK is hydrolyzed by both domains. Developing a C-domain selective inhibitor (RXPA380) would permit some degradation of BK by the N-domain; this degradation could be enough to prevent the accumulation of excess BK causing angioedema.

The well-known function of ACE is the conversion of Ang I to Ang II and the degradation of BK, which plays an important role in controlling the blood pressure. ACE also acts on other natural substrates, including encephalin, neurotensin, and substance P. Besides being involved in blood pressure control, ACE possesses widespread functions including renal development, male fertility, hematopoiesis, erythropoiesis, myelopoiesis, and immune responses. ACE2 can convert Ang II to Ang1–7, thereby reducing the concentration of Ang II and increasing that of Ang1–7. ACE2 can also convert Ang I to Ang1–9, which is subsequently converted into Ang1–7 by ACE. The high expression of ACE2 favors the balance of Ang1–7 over Ang II, which accounts for the cardioprotective role of ACE2 via the Ang1–7/Mas signaling pathway.

The inclusion (II) or deletion (DD) of the 287 bp Alu repeat in the 16th intron affects the human plasma ACE levels. The DD genotype is more frequently found in patients with myocardial infarction but no convincing evidence is available on the association of the DD genotype with hypertension. ACE2 was identified as the receptor for the SARS (severe acute respiratory syndrome) coronavirus. The SARS virus binding downregulates the cellular expression of ACE2, and the binding induces the clathrin-dependent internalization of the virus/receptor (SARS/ACE2) complex. Not only has ACE2 facilitated the invasion of the SARS virus for rapid replication, but also ACE2 is depleted from the cell membrane. Therefore, the damaging effects of Ang II are enhanced, resulting in the acute deterioration of lung tissues.

ACE possesses dual actions to convert Ang I to Ang II, and degrade bradykinin. The development of an ACE inhibitor was the first effective drug for hypertension caused by high renin activity. ACE2 was identified as the receptor for the SARS (severe acute respiratory syndrome) coronavirus, which caused an epidemic in 2002–2003. ACE was discovered in the mid-1950s through the observation that the dialysis of plasma and kidney extract with water and saline before incubation produced two separate pressor substances, Ang I and Ang II, respectively. It was discovered for a second time in 1966 during the characterization of a bradykinin (BK)-degrading enzyme from the kidney. This was named kininase II, which later was found to be the same enzyme as ACE. ACE2 was discovered in 2000 when two independent research groups cloned homologous ACE that could convert Ang I to Ang1–9 and yet also be captopril-insensitive.

Angiotensin converting enzyme from rabbit lung has been used:

• for measuring inhibitory effect of egg white protein hydrolysates on ACE activity by high performance liquid chromatography (HPLC)
• to measure the ACE inhibition by litchi pericarp and cooked chicken breast using hippuryl-L-histidyl-L-leucine (HHL) as substrate by reverse phase-HPLC (RP-HPLC)3 and HPLC respectively
• in releasing GPI anchored protein in vitro in few cell lines like HeLa, HEK293 and in vivo in mice sperm.

The angiotensin-converting enzyme (ACE) is a dipeptidyl-carboxypeptidase which exists in somatic and testicular isoforms with zinc binding motif HEXXH in their active site. ACE regulates blood pressure through renin-angiotensin system. ACE elevates blood pressure by converting angiotensin I to a key vasoconstrictor angiotensin II and inhibiting a potent vasodilator bradykinin. Inhibition of ACE is a targeted therapeutic strategy for high blood pressure. Several ACE synthetic inhibitory peptides available for clinical use include captopril, enalapril and lisinopril. Currently, developing inhibitory peptides from natural food sources, or phenolic compounds from plant sources to inhibit ACE is underway. ACE plays a critical role in fertilization by releasing the proteins anchored to glycosylphosphatidylinositol (GPI) in sperm membrane.

Removes C-terminal dipeptides from susceptible substrates, e.g., angiotensin I and bradykinin.

ACE has been the target of hypertension control since the 1970s. ACE inhibitors are prescribed as the sole or combinational treatment for high blood pressure, for its dual effects of lowering Ang II and slowing down BK degradation. In human hypertensive patients, ACE2 levels are lower in both the kidney and heart compared to normotensive volunteers.

Purify ACE by fractionation on DEAE-cellulose, Ca phosphate gel chromatography, elution from Sephadex G-200 and lectin affinity chromatography. The MW varied with glycosidation and is higher by gel filtration. It contains one atom of Zn/mol and has Km values for hydrolysis of hippurylhistidinylleucine and angiotensin I of 2.3 and 0.07 mM, and turnover of 15,430 and 792 mol/min/mol at 37o, respectively. The activity is inhibited by EDTA and increased amounts of Ca ions but required Ca ions. [Das & Soffer J Biol Chem 250 6762 1975, Reviewed by Ehlers & Riordan Biochemistry 28 5311 1989.]