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Generalities

The Aeromonas Sobria Serine Protease ASP protein is a serine protease that will cut peptide bonds after specific amino acids of a target protein. It preferentially cleaves peptide bonds that follow dibasic amino-acid residues. The kexin-like serine protease belongs to the subtilisin family (Subtilase). The structure of ASP is similar to that of Kex2 ^[1] (1r64), a protease of the subtilisin family, but ASP has a unique extra occluding region close to its active site.

This protein is secreted by the Anaerobic bacterium Aeromonas Sobria, which can cause potentially lethal septic shock. It is a clinical syndrome of potentially fatal organ dysfunction caused by a disorder in the response to infection. In septic shock, there is a critical reduction in tissue perfusion; acute multivisceral failure, including the lungs, kidneys and liver, can be observed. ^[2]

ASP is a sepsis-related factor. It can cause several dysfunction like by inducing vascular leakage, reducing blood pressure via the activation of the kinin system or promoting human plasma coagulation through the activation of prothrombin. Finally it can causes the formation of pus and edema through the action of anaphylatoxin C5a (4p3a). Gastroenteritis, and in extreme cases deuteropathy, are the main syndrome caused by infection with A.sobria.

Maturation of ASP

The precursor of ASP is composed of 624 amino acids. It contains a signal peptide of 24 amino-acids, a catalytic domain, similar to that of subtilisin, and a P domain. The maturation of ASP is achieved by ORF2. This protein plays the role of an external chaperone and is necessary for the construction of the stable ASP. Indeed, ASP doesn’t contain a propeptide (such as Kex2) that is involved in the proper folding of the protein. The ORF2 protein is composed of 152 amino-acids coded by the orf2 gene of 456 base pairs. The N-terminal extension and the C-terminal tail of the protein are implicated in the maturation of ASP. In fact, a complex ASP-ORF2 is formed. This association requires a specific organization of ASP in the space and more specifically the His595. The P-domain of ASP doesn’t bind to ORF2 but the sixth residue from the C-terminus domain of ORF2 interact with the

Phrase dans maturation à reformuler … “For maturation of ASP, the first 24 residues of the propeptide are cleaved and although a functional P-domain is reportedly necessary for maturation of the substitution domain in kexins”

Secondary structure

The structure of ASP is very similar to that of Kex2 (1r64), but it has a unique extra-occluding region close to its active site within the subtilisin domains. This extra-occluding region is unique and it could serve as a useful target to make the development of new antisepsis drugs easier.

The domain structure of ASP consists of the propeptide, the catalytic subtilisin-like domain, and the P-domain. The ASP molecule have two mean regions: an N-terminal region extending from Gly-3 to Pro-431 and forming the , and a C-terminal region extending from Leu-432 to His-595 and forming the .

Moreover, we can find three in the ASP Structure (Ca1, Ca2 and Ca3). are situated in the N-terminal domain, and is situated in the C-terminal domain. It were assigned to ASP based on electron density, counter charges, and coordination. But in contrary to Kex2, ASP contains no Ca2+ binding sites near its catalytic site.

Those Ca2+ binding Site are important because ...

Domains

The Subtilisin Domain: It contains 10 helices (alpha 1 to 10) and twelve chains (béta 1 to 10 and béta 13 to 14). The N-terminal domain of ASP seems to be like the catalytic domain of Kex2, which is similar to those of subtilisin and other subtilisin-related proteases. This ASP catalytic site contains Asp-78, His-115, and Ser-336 residues characteristic of subtilisins. In addition, 4 loops (L) protrude from the N-terminal subtilisin domain of ASP: Gly-3– Pro-26 (), Asn-221–Phe-241 (), Gly-300–Cys-326 (), and Gln-377–Glu-397 (). L1, L2, and L3 have random coil structure, whereas L4 forms a hairpin that protrudes toward the P-domain. Moreover, two are formed between Cys-4 and Cys-24 in L1 and between Cys-301 and Cys-326 in L3, which stabilize those loops.

The P-domain: The core of the P-domain in ASP contains 8 béta-strands (béta 16 18 23 and 26). The is comprised of two parts, (Gly 521–Thr 525, béta 5, 6, and 12) and (Gly-557–Asn-578, béta 25), and it is situated close to Asp-78,His-115,and Ser-336.

Active site

The catalytic triad: The catalytic triad of ASP is composed of Asp78, His115 and Ser336. These amino acids are the base is the active site of the protein, where the mode of action of the serine protease takes place. A peptide can be inserted in the space of the active site. There, the amino acids of will interact together and the mechanism will lead to a cut in the polypeptide.

Mechanism: The mechanism is the following: The histidine will react with the serine and deprotonate it. The deprotonated hydroxyl group of the serine will act as a nucleophilic species and attack the carbon from the carbonyl function on the peptide. This will lead to the formation of a tetrahedral intermediate. Then, a second tetrahedral intermediate will be formed, but with the attack of a deprotonated water molecule. At the end, the regeneration of the active site will be done with the release of the peptide cut in two parts.

Classification and properties

Performed experiments aimed to study the classification of ASP through inhibition, as well as the ability to enhance vascular permeability in dorsal skin tissue of rodents (Wistar rat).

ASP was shown not to be a metallo-protease, because its activity is not affected by metal chelators (EDTA, EGTA, o-phenantroline) or metallo-protease inhibitors (phosphoramidon). ^[3]

The ASP protease activity was strongly attenuated by serine protease inhibitors (DFP, AEBSEF).

NOT NECESSARY ?... ( suggesting a hypothetical belonging to the subtilisin serine proteases family. Furthermore the predicted amino acid sequence reinforces this speculation. However, the size of the ASP (MW 65000) is unlike other subtilisin proteases (MW 30000). Also the amino acid residues composition is different from the family’s characteristics because ASP shows unique cysteine residues that other family members don t show. Therefore we can state that it is likely that ASP belongs to the subtilisin serine proteases family, however it remains unclear.)

A soybean trypsin inhibitor was shown not to block the proteolytic action of ASP itself, but could inhibit the vascular permeability enhancing activity that follows after injection of ASP into epithelial cells. ^[4]

This experimental finding suggests that epithelial trypsin like proteases mediate the reaction causing enhanced vascular permeability. It is likely that ASP stimulates the secretion and maturation of epithelial trypsin proteases, thus enhancing the vascular permeability. ASP could stimulate the bradykinin-releasing pathway, thus stimulating mast cells to release histamine and further enhance the vascular permeability.

Antihistaminic agents (diphenhydramine and pyrilamine) were shown to efficiently inhibit the vascular permeability enhancing activity of the ASP. It is very likely that the vascular permeability enhancement is related to the release of histamine from mast cells. Through histopathological examinations it was shown that mast cells appeared around the injection site, confirming the role of histamine as a key factor.

Impact on human body

The most common form of desease is one where A.sobria pathogen adheres to the surface of the intestine causing painful diarrhoea, also known as gastroenteritis. The enterotoxic activity of the Hemolysin virulence factor of A.sobria contributes to those symptoms. However, the mortality due to intestinal disease type of infection is low compared to the non-intestinal diseases caused by A.sobria infection. Once invaded the intestine epithel cells, Aeromonas can reach any organ via the blood. Multiple virulence factors than promote their pathogenicity.

The nonintestinal form of the disease reports symptoms such as septicaemia, lesions of skin and soft tissues as well as meningitis, often ending fatally.

leading to crucial reduction in tissue perfusion followed by fatal organ disfunction.

The ASP induced proteolysis digestion of proteins like kininogen, prothrombin, fibrinogen or prekallikrein at restricted sites generates fragments, expressing their own activity and therefore inducing specific physiological reactions. The kinin system activation for example reduces the blood pressure while the prothrombin system promotes plasma coagulation.

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