Supramolecular chiral nanocarriers successfully immobilize GOx and realize overall conformational optimization of GOx via enhanced stereoselective binding, efficiently improving GOx catalytic activity as well as tumor therapeutic efficiency.
Achieving a continuous range of helical pitches, remains a formidable challenge, as conventional methods typically rely on complex multicomponent systems that suffer from chemical heterogeneity and limited predictability.
A chiral supramolecular biomaterial (L-/D-phenylalanine and D-phenylalanine, L/DP) is rationally designed with defined chiral nanostructure and optical activity for hypertrophic scars (HS) therapy.
Natural protein condensates respond to external stresses through stimuli-triggered multistage phase transitions. Reprogramming such transitions in synthetic systems is critical for rational design of self-adaptive materials with precisely regulated stimuli-responsiveness.
In situ precise matching of chiral structures (e.g., stereocomplementary pairs between secondary structures of proteins) is essential for directing the evolution of biostructures.
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