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Pregled bibliografske jedinice broj: 856905

Computational study of the substrate specificity of monoamine oxidase B


Maršavelski, Aleksandra; Vianello, Robert
Computational study of the substrate specificity of monoamine oxidase B // ECS3 Book of Abstracts
Bol, Brač, Hrvatska, 2016. str. 7-7 (poster, međunarodna recenzija, sažetak, ostalo)


CROSBI ID: 856905 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Computational study of the substrate specificity of monoamine oxidase B

Autori
Maršavelski, Aleksandra ; Vianello, Robert

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo

Izvornik
ECS3 Book of Abstracts / - , 2016, 7-7

Skup
3rd European Crystallography School

Mjesto i datum
Bol, Brač, Hrvatska, 25.09-02.10.2016

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
MAO B, MM-PBSA, MD, QM

Sažetak
Histamine plays an important role in the human body and is involved in more than twenty different physiological processes. Due to histamine potent physiological activity, its degradation has to be carefully regulated to avoid adverse reactions. The major routes of histamine inactivation in mammals include monoamine oxidase B (MAO B) and diamine oxidase (DAO) enzymes. The fact that MAO B metabolizes only N-methylhistamine while DAO prefers histamine, pinpoints their remarkable selectivity towards two compounds that differ only in one methyl group. The mechanism of enzyme catalysis and specificity are usually elucidated from the differences in mechanistic aspects of enzymatic reactions for each possible subs trate, which provide unambiguous quantitative information about the thermodynamics and the kinetics of reaction pathways. Unfortunately, mechanistic studies are not always experimentally approachable. Therefore, we utilized a combination of molecular dynamics (MD) simulations, MM-PBSA binding free energy calculations and quantum mechanical cluster approach to address substrate specificity and mechanism of MAO B catalysis. We have identified favourable Hydrophobic interactions between methyl group of the N-methylhistamine substrate and the hydrophobic side chains of the enzyme binding site that keep substrate anchored and properly oriented for the enzymatic reaction. Since histamine is deprived of methyl group it cannot be properly anchored and rotates within the active site, which results in non-productive orientation for the reaction. Quantum-chemical mechanistic analysis within the cluster model of the enzyme revealed higher activation parameters for histamine relative to its N-methyl counterpart, thus aid ing in rationalizing the mentioned selectivity. Inspection of the calculated free-energy profiles (Figure 1.) convincingly shows that MAO B selectivity for the N-methylhistamine over histamine is a result of two synergistic effects: lower activation barrier and more favourable reaction thermodynamics. Moreover, reaction pathway obtained from QM calculations is consistent with recently proposed hydride mechanism of MAO B mechanism of catalysis

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Ustanove:
Institut "Ruđer Bošković", Zagreb

Citiraj ovu publikaciju

Maršavelski, Aleksandra; Vianello, Robert
Computational study of the substrate specificity of monoamine oxidase B // ECS3 Book of Abstracts
Bol, Brač, Hrvatska, 2016. str. 7-7 (poster, međunarodna recenzija, sažetak, ostalo)
Maršavelski, A. & Vianello, R. (2016) Computational study of the substrate specificity of monoamine oxidase B. U: ECS3 Book of Abstracts.
@article{article, year = {2016}, pages = {7-7}, keywords = {MAO B, MM-PBSA, MD, QM}, title = {Computational study of the substrate specificity of monoamine oxidase B}, keyword = {MAO B, MM-PBSA, MD, QM}, publisherplace = {Bol, Bra\v{c}, Hrvatska} }
@article{article, year = {2016}, pages = {7-7}, keywords = {MAO B, MM-PBSA, MD, QM}, title = {Computational study of the substrate specificity of monoamine oxidase B}, keyword = {MAO B, MM-PBSA, MD, QM}, publisherplace = {Bol, Bra\v{c}, Hrvatska} }




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