C1-inhibitor

Serpin peptidase inhibitor, clade G (C1 inhibitor), member 1
C1-inhibitor
Available structures PDB Ortholog search: PDBe, RCSB List of PDB id codes 1M6Q​, 2OAY​
Identifiers
Symbols	SERPING1 ; C1IN; C1INH; C1NH; HAE1; HAE2
External IDs	OMIM: 606860 MGI: 894696 HomoloGene: 44 GeneCards: SERPING1 Gene
Gene ontology Molecular function • serine-type endopeptidase inhibitor activity • protein binding Cellular component • extracellular region • extracellular space • platelet alpha granule lumen • extracellular exosome • blood microparticle Biological process • negative regulation of complement activation, lectin pathway • platelet degranulation • complement activation, classical pathway • aging • blood coagulation • blood coagulation, intrinsic pathway • blood circulation • negative regulation of endopeptidase activity • platelet activation • fibrinolysis • innate immune response Sources: Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	710	12258
Ensembl	ENSG00000149131	ENSMUSG00000023224
UniProt	P05155	P97290
RefSeq (mRNA)	NM_000062	NM_009776
RefSeq (protein)	NP_000053	NP_033906
Location (UCSC)	Chr 11: 57.6 – 57.61 Mb	Chr 2: 84.77 – 84.78 Mb
PubMed search

C1-inhibitor (C1-inh, C1 esterase inhibitor) is a protease inhibitor belonging to the serpin superfamily. Its main function is the inhibition of the complement system to prevent spontaneous activation.^[1][2] C1-inhibitor is an acute-phase protein that circulates in blood at levels of around 0.25 g/L. The levels rise ~2-fold during inflammation. C1-inhibitor irreversibly binds to and inactivates C1r and C1s proteases in the C1 complex of classical pathway of complement. MASP-1 and MASP-2 proteases in MBL complexes of the lectin pathway are also inactivated. This way, C1-inhibitor prevents the proteolytic cleavage of later complement components C4 and C2 by C1 and MBL. Although named after its complement inhibitory activity, C1-inhibitor also inhibits proteases of the fibrinolytic, clotting, and kinin pathways. Note that C1-inhibitor is the most important physiological inhibitor of plasma kallikrein, fXIa, and fXIIa.

Proteomics

C1-inhibitor is the largest member among the serpin superfamily of proteins. It can be noted that, unlike most family members, C1-inhibitor has a 2-domain structure. The C-terminal serpin domain is similar to other serpins, which is the part of C1-inhibitor that provides the inhibitory activity. The N-terminal domain (also some times referred to as the N-terminal tail) is not essential for C1-inhibitor to inhibit proteases. This domain has no similarity to other proteins. C1-inhibitor is highly glycosylated, bearing both N- and O-glycans. N-terminal domain is especially heavily glycosylated.^[2]

Genetics

The human C1-inhibitor gene (SERPING1) is located on the eleventh chromosome (11q11-q13.1).^[3][4]

Role in disease

Deficiency of this protein is associated with hereditary angioedema ("hereditary angioneurotic edema"), or swelling due to leakage of fluid from blood vessels into connective tissue.^[5] Deficiency of C1-inhibitor permits plasma kallikrein activation, which leads to the production of the vasoactive peptide bradykinin. Also, C4 and C2 cleavage goes unchecked, resulting in auto-activation of the complement system. In its most common form, it presents as marked swelling of the face, mouth and/or airway that occurs spontaneously or to minimal triggers (such as mild trauma), but such swelling can occur in any part of the body. In 85% of the cases, the levels of C1-inhibitor are low, while in 15% the protein circulates in normal amounts but it is dysfunctional. In addition to the episodes of facial swelling and/or abdominal pain, it also predisposes to autoimmune diseases, most markedly lupus erythematosus, due to its consumptive effect on complement factors 3 and 4. Mutations in the gene that codes for C1-inhibitor, SERPING1, may also play a role in the development of age related macular degeneration.^[6]

Despite uncontrolled auto-activation, it is important to note that levels of key complement components are low during an acute attack, because they are being consumed - indeed, low levels of C4 are a key diagnostic test for hereditary angioedema. This situation is analogous to the low levels of clotting factors found in disseminated intravascular coagulation (DIC).

Classification

There are three types of C1 inhibitor deficiency:^[7]

• Type I: Hereditary. Three of the four genes for C1 inhibitor are null genes, leading to low levels of C1 inhibitor.
• Type II: Hereditary. There are high levels of C1 inhibitor, but it is non-functional.
• Type III: Hereditary or acquired. Related to hormone levels in the body.

Therapeutic use

In hereditary angioedema

People with frequent attacks of angioedema are often treated using attenuated androgens, such as danazol and oxandrolone. Blood-derived C1-inhibitor may be more effective and does not carry the side-effects of danazol such as virilization and a risk of liver tumors, but does carry the risk associated with the use of any human blood product. Cinryze, a pharmaceutical-grade C1-inhibitor, was approved for the use of HAE in 2008. It was also the first C1-inhibitor approved for use in the United States.^[8] It is a highly purified, pasteurized and nanofiltered plasma-derived C1 esterase inhibitor product; it has been approved for routine prophylaxis against angioedema attacks in adolescent and adult patients with HAE.^[9]

A recombinant C1 inhibitor obtained from the milk of transgenic rabbits, conestat alfa (trade name Ruconest), is approved for the treatment of acute HAE attacks in adults.^[10][11]

While C1 inhibitor therapy has been used acutely for more than 35 years in Europe in patients with C1 inhibitor deficiency, new methods of treating acute attacks have emerged: a plasma kallikrein inhibitor and the bradykinin receptor antagonist icatibant.

For other conditions

The activation of the complement cascade can cause damage to cells, therefore the inhibition of the complement cascade can work as a medicine in certain conditions.^[12] When someone has a heart attack, for instance, the lack of oxygen in heart cells causes necrosis in heart cells: Dying heart cells spill their contents in the extracellular environment, which triggers the complement cascade. Activation of the complement cascade attracts phagocytes that leak peroxide and other reagents, which may increase the damage for the surviving heart cells. Inhibition of the complement cascade can decrease this damage.

Synthesis

C1-inhibitor is contained in the human blood; it can, therefore, be isolated from donated blood. Risks of infectious disease transmission (viruses, prions, etc.) and relative expense of isolation prevented widespread use. It is also possible to produce it by recombinant technology, but Escherichia coli (the most commonly used organism for this purpose) lacks the eukaryotic ability to glycosylate proteins; as C1-inhibitor is particularly heavily glycosylated, this asialylated recombinant form would have a short circulatory life (the carbohydrates are not relevant to the inhibitor function). Therefore, C1-inhibitor has also been produced in glycosylated form using transgenic rabbits.^[13] This form of recombinant C1-inhibitor also has been given orphan drug status for delayed graft function following organ transplantation and for capillary leakage syndrome.^[14]

References

Further reading

External links

• The MEROPS online database for peptidases and their inhibitors: I04.024
• B02AB03

PDB gallery 2oay: Crystal structure of latent human C1-inhibitor