HAMMEROVÁ, Zuzana, Josef HOUSER, Stanislav KOZMON, Deepti MISHRA, Jaroslav KOČA and Michaela WIMMEROVÁ. Carbohydrate-protein binding site interaction. In XIX. setkání biochemiků a molekulárních biologů. 2018. ISBN 978-80-210-9069-9.
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Basic information
Original name Carbohydrate-protein binding site interaction
Authors HAMMEROVÁ, Zuzana (203 Czech Republic, belonging to the institution), Josef HOUSER (203 Czech Republic, belonging to the institution), Stanislav KOZMON (703 Slovakia, belonging to the institution), Deepti MISHRA (356 India, belonging to the institution), Jaroslav KOČA (203 Czech Republic, guarantor, belonging to the institution) and Michaela WIMMEROVÁ (203 Czech Republic).
Edition XIX. setkání biochemiků a molekulárních biologů, 2018.
Other information
Original language English
Type of outcome Conference abstract
Field of Study 10201 Computer sciences, information science, bioinformatics
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14310/18:00105744
Organization unit Faculty of Science
ISBN 978-80-210-9069-9
Keywords in English carbohydrate; sugar; protein complexes; CH-pi stacking
Changed by Changed by: Mgr. Zuzana Hammerová, učo 393906. Changed: 20/1/2019 17:16.
Abstract
Interactions of saccharides with receptors belong to the most important ones in cell recognition, growth or differentiation, as well as in many pathological processes. These interactions are mediated by so-called glycocode – saccharide code which is read by many proteins. Saccharides interact with proteins in various ways. The most famous are hydrogen bridges but saccharides utilize also hydrophobic interactions or metal-ion mediated interaction. We concentrated mainly on CH-pi stacking interaction – the dispersion driven interaction between carbohydrate apolar faces and aromatic amino-acid residues. This interaction has been underestimated for a long time but we found out that it is a highly important interaction in carbohydrate-protein complexes. In our computational structure-based study we examined structures stored in Protein Data Bank (PDB) database. We examined complexes with a carbohydrate in a close proximity of an aromatic amino acid (tryptophan, tyrosine, phenylalanine, and histidine). We detected the presence of CH-pi stacking and examined the geometry parameters of these binding sites. Each aromatic amino acid showed a unique CH-pi stacking pattern, demonstrated by a characteristic orientation, bond distances, and bond angles between the carbohydrate and a particular amino acid. Besides CH-pi stacking interaction, we detected also hydrogen bridges and compare the frequencies of these two types of carbohydrate-protein interaction. These results provide insight into the importance of CH-pi stacking in carbohydrate-protein interactions and may help in drug development, receptor studies or protein engineering.
Links
LQ1601, research and development projectName: CEITEC 2020 (Acronym: CEITEC2020)
Investor: Ministry of Education, Youth and Sports of the CR
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