Autor: |
Dr. Giada Beltrami, Prof. Annalisa Martucci, Prof. Luisa Pasti, Dr. Tatiana Chenet, Dr. Matteo Ardit, Dr. Lara Gigli, Dr. Mirco Cescon, Dr. Emmanuelle Suard |
Jazyk: |
angličtina |
Rok vydání: |
2020 |
Předmět: |
|
Zdroj: |
ChemistryOpen, Vol 9, Iss 10, Pp 978-982 (2020) |
Druh dokumentu: |
article |
ISSN: |
2191-1363 |
DOI: |
10.1002/open.202000183 |
Popis: |
Abstract Combined neutron and X‐ray powder diffraction techniques highlighted the sorption capacity of the acidic L zeolite towards the L‐lysine amino acid. The role of zeolite channels in the stabilization of the lysine absorbed and the effect of water on protein structure are elucidated at atomistic level. The stabilization of the L α‐helical conformation is related to strong H‐bonds between the tail aminogroups of lysine molecules and the Brønsted acid site as well as to complex intermolecular H‐bond system between water molecules, zeolite and amino acid. This finding is relevant in the catalytic synthesis of polypeptide, as well as in industrial biotechnology by qualitatively predicting binding behaviour |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
|
Nepřihlášeným uživatelům se plný text nezobrazuje |
K zobrazení výsledku je třeba se přihlásit.
|