Dynamic bond-driven encapsulation of enzymes in metal–organic frameworks beyond pore size constraints

Dynamic bond-driven encapsulation of enzymes in metal–organic frameworks beyond pore size constraints

Metal–organic frameworks with dynamic metal–ligand bonds form reversible gates that admit enzymes larger than the pores, enabling stable encapsulation and efficient multi-enzyme cascade catalysis for glycan precursor synthesis.

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    Dynamic bond-driven encapsulation of enzymes in metal–organic frameworks beyond pore size constraints - FHMnews