My research exploring peptide functionalization, focusing on self-assembly, biofunctionalization fibers, hydrogels, and responsible separations. This video describe how ECF-5 peptides self-assembly in response to environmental change and the process of generating peptide hydrogels. Compared to traditional polymer hydrogels, peptide hydrogels are for diverse field biofunctions and separate biocompatibility, enhancing their potential in field like biomedical engineering and biomaterials.
Technological breakthroughs in this field focused on improving self-assembly performance and biofunctionalization. include peptide hydrogels with non-nature amino acid, faster point chemical medication, and eluting specific biofunctionalized peptides, thereby enhance their drug-forming and biofunctional purposes. Current peptide drug-forming method have high experimental demands and lack universality.
Developing self-assembly hydrogel formation methods using common operations and regions will better support the widespread application of peptide hydrogels. Using the ECF-5 peptide, we added phase three, generalized the environmentally responsive calcium methods. This methods rotating the peptide surface and properties.
We are adding design other self-assembling peptide with improved calcium control. To begin the pH response method for hydrogel formation, add five milligrams of ECF-5 peptides to 400 microliters of deionized water and sonicate it at 40 kilohertz for 30 minutes, Add 40 microliters of filtered one molar sodium hydroxide to the peptide solution and vortex to mix thoroughly. Continue sonication for 15 more minutes until the solution is completely clarified.
Next, add 60 microliters of hydrochloric acid to the prepared solution. After vortexing the mixture, let it stand at room temperature for over 30 minutes to facilitate hydrogel formation. To begin, prepare an ECF-5 self-assembling peptide solution at a concentration of 10 milligrams per milliliter using a suitable buffer.
Sonicate the mixture to dissolve the peptide and store it at four degrees Celsius. Prepare a 50 milligrams per milliliter calcium chloride solution using deionized water. Add 40 microliters of calcium chloride solution to 460 microliters of the ECF-5 peptide solution.
Vortex to mix thoroughly and incubate the mixture at room temperature for over two hours. Rapidly introduce one milliliter of PBS into the dimethyl sulfoxide, or DMSO solubilized peptide. Vortex thoroughly and incubate at room temperature.
After five minutes, add 500 microliters of PBS and let the mixture stand for 15 minutes, then discard the supernatant and retain the bottom gel. The ECF-5 peptide displayed glutathione-like reducing properties and self-assembly capability, forming a solid gel within minutes when the concentration exceeded 1%The ECF-5 hydrogel exhibited semi-solid properties when prepared via pH response, metal addition, or solvent exchange. To begin, prepare the peptide hydrogels using a suitable method.
Apply double-sided adhesive to remove a layer of mica and adhere the mica surfaces using the APTES solution and let it stand for five minutes. Rinse the mica surfaces thoroughly with pure water before use. Dilute the hydrogel and mix it thoroughly before dropping it onto the modified mica surface for static absorption.
After five minutes, rinse the surface with pure water and dry it. Atomic force microscopy revealed that the gel surface had numerous peptide fibers with dense pores trapping water, with individual fibers forming consistent wider fiber bands approximately 3.5 nanometers in height.
