Recently, the role of molecular control in the tooth mineralization process has received much attention. Biomimetic scaffolds have been started to use in dental tissue engineering and regeneration due to their high applicability, biocompatibility, biodegradability, and mineralization capability. In this thesis, a hybrid biomimetic bio-ink; P11-4 peptide-based Quince Seed Hydrogel (QSH)/Gelatin (Gel) is used in 3D cell culture studies for dental tissue engineering applications. Pristine QSH, QSH/Gel, and P11-4/QSH/Gel bio-inks were characterized by FTIR and viscosity analysis, and their 3D bioprinting parameters were optimized. Hydrogels were crosslinked via 1-Ethyl-3-(3-dimethylaminopropyl) Carbodiimide (EDC)/N-Hydroxysuccinimide (NHS) coupling reaction and various hydrogel concentrations were investigated for scaffold fabrication. Characterization of produced scaffolds was performed by SEM imaging, mechanical testing, protein adsorption, and swelling analyses. As a result, the mechanical strength, viscosity, swelling properties, and surface characteristics of the biomaterial were evaluated. SaOS-2 human osteosarcoma cell line was used for 3D bioprinting studies. Cell viability analyses were performed via Live/Dead and MTT assays. Mineralization was investigated and assay was carried out with Alizarin Red Staining. According to obtained results, P11-4/QSH/Gel scaffolds provide high cell viability and proliferation rate compared to pristine QSH and QSH/Gel control groups. Also, with the addition of P11-4 to QSH/Gel, a certain amount of increase in mineralization was observed after day 7 on long-term cultured scaffolds. As a result of this study, it was concluded that P11-4-based QSH/Gel has a high potential to be used as a bio-ink in the production of 3D scaffolds for dental tissue engineering applications.