An interpenetrating polymer-silica network improves fluorescence brightness, photostability, and colloidal stability for biological probes.
Engineered HlyA fusion variants improve recombinant protein solubility, proteolytic stability, secretion yield, and renaturation efficiency.
Targeted AhpD core-domain mutation improves peroxide response in recombinant strains, raising L-glutamic acid fermentation yield.
Directing Brazzein secretion into the culture medium raises yield and simplifies purification by avoiding periplasmic extraction steps.
Novel yeast promoters replace methanol induction to cut cost, shorten fermentation, and avoid peroxide-related protein degradation.
EcPhnD binding-pocket mutations enable reagentless fluorescent glyphosate detection with high sensitivity and reusable sensing.
Engineered restriction sites and ligation steps convert display vectors into expression vectors with over 90% efficiency, speeding binder characterization.
A fused scMagnet links pMag and nMag in one polypeptide to boost light-controlled split protein binding with minimal leak activity.
Amino acid substitutions in IL-2 shift receptor binding to stimulate or inhibit Tregs while reducing toxicity and dosing burden.
A purified thaumatin II and brazzein ratio improves sweetness synergy, cuts bitter off-notes, and delivers a better temporal profile.
Engineered Enterobacteriaceae overexpress tdh and kbl to ferment and accumulate γ-Glu-Val-Gly more efficiently than complex synthesis routes.
Engineered PapG mRNA-LNP antigens lower ligand binding while preserving immunogenicity, enabling scalable E. coli vaccine development.
D-amino acid peptides bind HLA-DQ8 to block InsB:9-23 presentation, limiting T-cell attack on beta cells without systemic immunosuppression.