Biological Selection of Peptides for Poly(l-lactide) Substrates

Short peptides that recognize the α form of poly(l-lactide) (PLLA) crystalline films were identified from a phage-displayed peptide library. An enzyme-linked immunosorbent assay (ELISA) revealed that the apparent binding constants of the phage clones for the α form of PLLA were greater than those of the unselected phage library. The specificity index for the α form of PLLA referred to a structurally similar atactic poly(methyl methacrylate) (at-PMMA), supporting the α form of PLLA specific binding of the selected phage. Amino acid residues with proton-donor lateral groups and hydrophobic alkyl groups were relatively enriched in a sequence of heptapeptides on the specific phage clones, thereby suggesting the presence of hydrogen bonding as well as hydrophobic interactions between the α form of PLLA and the peptides. Surface plasmon resonance (SPR) analysis revealed that the binding constant of the freed c22 heptapeptide (Gln-Leu-Met-His-Asp-Tyr-Arg) for the α form of PLLA was greater than those for reference at-PMMA, amorphous PLLA, and the β form of PLLA. It was found that c22 peptide can recognize slight differences in PLLA polymorphs such as a crystalline state and an arrangement of PLLA functional groups

Peptide-Based Switching of Polymer Fluorescence in Aqueous phase

Peptide-Based Switching of Polymer Fluorescence in Aqueous phas

Simultaneous Enhancement of Cell Proliferation and Thermally Induced Harvest Efficiency Based on Temperature-Responsive Cationic Copolymer-Grafted Microcarriers

The development of large-scale suspension cell cultures using microcarriers has long been a focus of attention in the fields of pharmacy and biotechnology. Previously, we developed cell-detachable microcarriers based on temperature-responsive poly­(<i>N</i>-isopropylacrylamide) (PIPAAm)-grafted beads, on which adhering cells can be noninvasively harvested by only reducing the temperature without the need for proteolytic enzyme treatment. In this study, to improve the cell harvest efficiency from bead surfaces while maintaining cell adhesion and proliferation properties, we prepared temperature-responsive cationic copolymer-grafted beads bearing a copolymer brush consisting of IPAAm, positively charged quaternary amine monomer (3-acrylamidopropyl trimethylammonium chloride; APTAC), and hydrophobic monomer (<i>N</i>-<i>tert</i>-butylacrylamide; tBAAm). The incorporation of positively charged APTAC into the grafted copolymer brush facilitated bead dispersibility in a cell culture system containing Chinese hamster ovary (CHO-K1) cells and consequently allowed for enhanced cell proliferation in the system compared to that of unmodified CMPS and conventional PIPAAm homopolymer-grafted beads. Additionally, P­(IPAAm-<i>co</i>-APTAC-<i>co</i>-tBAAm) terpolymer-grafted beads exhibited the most rapid and efficient cell detachment behavior after the temperature was reduced to 20 °C, presumably because the highly hydrated APTAC promoted the overall hydration of the P­(IPAAm-<i>co</i>-APTAC-<i>co</i>-tBAAm) chains. Therefore, P­(IPAAm-<i>co</i>-APTAC-<i>co</i>-tBAAm) terpolymer-grafted microcarriers are effective in facilitating both cell proliferation and thermally induced cell detachment in a suspension culture system

Mechanochromic Dynamic Covalent Elastomers: Quantitative Stress Evaluation and Autonomous Recovery

Stress evaluation in polymeric materials is important in order to not only spot danger in them before serious failure, but also precisely interpret the destructive mechanism, which can improve the lifetime and durability of polymeric materials. Here, we are able to visualize stress by color changes, as well as quantitatively estimate the stress in situ, in segmented polyurethane elastomers with diarylbibenzofuranone-based dynamic covalent mechanophores. We prepared films of the segmented polyurethanes, in which the mechanophores were incorporated in the soft segments, and efficiently activated them by mechanical force. Cleavage of the mechanophores during uniaxial elongation and their recovery after the removal of the stress were quantitatively evaluated by in situ electron paramagnetic resonance measurements, accompanied by drastic color changes

Mechanochromic Dynamic Covalent Elastomers: Quantitative Stress Evaluation and Autonomous Recovery

Stress evaluation in polymeric materials is important in order to not only spot danger in them before serious failure, but also precisely interpret the destructive mechanism, which can improve the lifetime and durability of polymeric materials. Here, we are able to visualize stress by color changes, as well as quantitatively estimate the stress in situ, in segmented polyurethane elastomers with diarylbibenzofuranone-based dynamic covalent mechanophores. We prepared films of the segmented polyurethanes, in which the mechanophores were incorporated in the soft segments, and efficiently activated them by mechanical force. Cleavage of the mechanophores during uniaxial elongation and their recovery after the removal of the stress were quantitatively evaluated by in situ electron paramagnetic resonance measurements, accompanied by drastic color changes