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Biomimetic modelling of the (mononuclear) metalloenzyme active site (CROSBI ID 657983)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Višnjevac, Aleksandar Biomimetic modelling of the (mononuclear) metalloenzyme active site // 12th International Symposium on the Chemistry of Natural Compounds : Book of Abstracts / Sagdullaev, Sh. ; Baser, K. H. C. ; Aisa, H. A. (ur.). Taškent: Institute Sobir Junusov : Akademija znanosti i umjetnosti Uzbekistana, 2017. str. 14-14

Podaci o odgovornosti

Višnjevac, Aleksandar

engleski

Biomimetic modelling of the (mononuclear) metalloenzyme active site

Although bioinorganic chemistry examines the role that, generally, metallic and nonmetallic elements beyond the big six (CHNOPS) play in biological systems, metalloenzymes and metalloproteins remain its main topic [1]. Biomimetic chemistry aims to create novel chemical species inspired by the natural systems such as metalloenzymes. This translates to the catalysts design, but en-route, very often secrets of the mechanisms used by the natural systems are discovered [2]. As an example of the supramolecular approach in biomimetic modelling [3], the syntheses, structural characterizations, and chemical activity studies of "bowl complexes”, based on the resorcin[4]arene scaffold with three imidazole-containing coordinating arms grafted at the large rim, are presented. These complexes are biomimetic models of a ubiquitous mononuclear active site where three amino-acid residues hold the metal ion, leaving its one or two coordination sites available for the reversible guest (substrate) binding. The trisimidazole ligand RIm3 was prepared [4], as well as its complexes with Zn(II), Cu(I) [5] and Cu(II). Spectroscopic studies and X-ray single crystal analysis revealed a 5-coordinate environment for the Zn(II) and Cu(II) centres provided by three imidazole arms, and two extra donors, one embedded inside the resorcinarene cavity, the other in exo position. These two labile sites are occupied by solvent molecules or residual water, and are readily displaced by carboxylate donors, the position of which (endo or exo) is under tight control of the bowl-cavity. The reaction of RIm3 ligand with Zn(II) or Cu(II) acetates led to the formation of the complexes with the acetate anion irreversibly embedded inside the cavity. Cu(II) acetate complex was characterized by the X-ray single crystal analysis [6]. Its molecular structure features a rigidified resorcinarene bowl, which reveals an approximate, non-crystallographic, 4mm point symmetry, and can easily host small guest molecules.

biomimetic ; bioinorganic ; resorcinarene ; X-ray single crystal

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Podaci o prilogu

14-14.

2017.

objavljeno

Podaci o matičnoj publikaciji

12th International Symposium on the Chemistry of Natural Compounds : Book of Abstracts

Sagdullaev, Sh. ; Baser, K. H. C. ; Aisa, H. A.

Taškent: Institute Sobir Junusov : Akademija znanosti i umjetnosti Uzbekistana

Podaci o skupu

12th International Symposium on the Chemistry of Natural Compounds

ostalo

07.09.2017-08.09.2017

Taškent, Uzbekistan

Povezanost rada

Kemija