Analysis of gelatin secondary structure in gelatin/keratin-based biomaterials
Year: 2023
Authors: Pulidori E., Micalizzi S., Koutsomarkos N., Bramanti E., Tinè MR., Vozzi G., De Maria C., Chatzinikolaidou M., Duce C.
Autors Affiliation: Univ Pisa, Dept Chem & Ind Chem, Via G Moruzzi 13, I-56124 Pisa, Italy; Univ Pisa, Res Ctr Piaggio, Dept Informat Engn, Largo L Lazzarino 1, I-56126 Pisa, Italy; Univ Pisa, Dept Informat Engn, Largo L Lazzarino 1, I-56126 Pisa, Italy; CNR, Inst Chem Organometall Cpds, Via G Moruzzi 1, I-56124 Pisa, Italy; INO CNR UOS Pisa, Natl Inst Opt, Via G Moruzzi 1, I-56124 Pisa, Italy; Univ Crete, Dept Mat Sci & Technol, IESL FORTH Heraklion, Iraklion, Crete, Greece.
Abstract: The possibility of using protein-based materials as cellular scaffold strongly depends on protein confor-mation, and several attempts have been made by researchers to obtain scaffold with morphology mim-ing the extracellular matrix. It is widely recognized that the secondary structure of proteins affects the mechanical and biological properties of protein-based scaffolds. However, few studies have been pub-lished, and an exhaustive explanation is still missing. In this work the study of the gelatin structure in gelatin-based materials and the investigation of the possible correlations between structure, mechanical and biological features is reported. We have examined how the secondary structure of gelatin is affected (i) by the process used to ob-tain the biomaterials (solvent casting vs. electrospinning), (ii) by the concentration of cross linker (3-(Glycidyloxypropyl)trimethoxysilane) (GPTMS), and (iii) by the raw keratin extract added. Gelatin electro-spun materials have shown a content of ordered structure higher than gelatin casted films, likely due to the random coil – alpha-helix transition occuring during electrospinning. GPTMS gives a decrease of ordered structures in gelatin casted films (random structure increasing from 20% to 60%), while it does not affect the percentage of ordered structure in electrospun samples. In the gelatin/keratin electrospun biomateri-als, the presence of keratin produces a decrease of alpha-helix content from 31% to 2-15% and an increase of beta-structures, promoting the conversion from antiparallel to parallel beta-sheet. The structure of gelatin affects the mechanical performances of biomaterials. In gelatin/keratin electrospun biomaterials we have found a positive correlation between failure strain and helix conformation and a negative correlation with beta-structures. Elastic modulus has opposite correlations. All gelatin-based biomaterials have been tested as scaffold for pre-osteoblastic cells showing good biocompatibility for both casted films and electrospun biomaterials. (c) 2023 Elsevier B.V. All rights reserved.
Journal/Review: JOURNAL OF MOLECULAR STRUCTURE
Volume: 1279 Pages from: 134984-1 to: 134984-10
KeyWords: Gelatin; Protein secondary structure; Electrospun; Mechanical properties; Bioactivity; Infrared spectroscopyDOI: 10.1016/j.molstruc.2023.134984Citations: 10data from “WEB OF SCIENCE” (of Thomson Reuters) are update at: 2024-12-08References taken from IsiWeb of Knowledge: (subscribers only)Connecting to view paper tab on IsiWeb: Click hereConnecting to view citations from IsiWeb: Click here