Self-assembled biomaterials are an important class of materials that can be injected and formed in situ. However, they often are not able to meet the mechanical properties necessary for many biological applications, losing mechanical properties at low strains. We synthesized hybrid hydrogels consisting of a poly(?-glutamic acid) polymer network physically cross-linked via grafted self-assembling beta-sheet peptides to provide non-covalent cross-linking through beta-sheet assembly, reinforced with a polymer backbone to improve strain stability. By altering the beta-sheet peptide graft density and concentration, we can tailor the mechanical properties of the hydrogels over an order of magnitude range of 10200 kPa, which is in the region of many soft tissues. Also, due to the ability of the non-covalent beta-sheet cross-links to reassemble, the hydrogels can self-heal after being strained to failure, in most cases recovering all of their original storage moduli. Using a combination of spectroscopic techniques, we were able to probe the secondary structure of the materials and verify the presence of beta-sheets within the hybrid hydrogels. Since the polymer backbone requires less than a 15% functionalization of its repeating units with beta-sheet peptides to form a hydrogel, it can easily be modified further to incorporate specific biological epitopes. This self-healing polymer-beta-sheet peptide hybrid hydrogel with tailorable mechanical properties is a promising platform for future tissue-engineering scaffolds and biomedical applications.