Aptamer‐Modified Homogeneous Catalysts, Heterogenous Nanoparticle Catalysts, and Photocatalysts: Functional “Nucleoapzymes”, “Aptananozymes”, and “Photoaptazymes”

Abstract Conjugation of aptamers to homogeneous catalysts (“nucleoapzymes”), heterogeneous nanoparticle catalysts (“aptananozymes”), and photocatalysts (“photoaptazymes”) yields superior catalytic/photocatalytic hybrid nanostructures emulating functions of native enzymes and photosystems. The concentration of the substrate in proximity to the catalytic sites (“molarity effect”) or spatial concentration of electron‐acceptor units in spatial proximity to the photosensitizers, by aptamer–ligand complexes, leads to enhanced catalytic/photocatalytic efficacies of the hybrid nanostructures. This is exemplified by sets of “nucleoapzymes” composed of aptamers conjugated to the hemin/G‐quadruplex DNAzymes or metal–ligand complexes as catalysts, catalyzing the oxidation of dopamine to aminochrome, oxygen‐insertion into the Ar─H moiety of tyrosinamide and the subsequent oxidation of the catechol product into aminochrome, or the hydrolysis of esters or ATP. Also, aptananozymes consisting of aptamers conjugated to Cu 2+ ‐ or Ce 4+ ‐ion‐modified C‐dots or polyadenine‐stabilized Au nanoparticles acting as catalysts oxidizing dopamine or operating bioreactor biocatalytic cascades, are demonstrated. In addition, aptamers conjugated to the Ru(II)–tris‐bipyridine photosensitizer or the Zn(II) protoporphyrin IX photosensitizer provide supramolecular photoaptazyme assemblies emulating native photosynthetic reaction centers. Effective photoinduced electron transfer followed by the catalyzed synthesis of NADPH or the evolution of H 2 is demonstrated by the photosystems. Structure–function relationships dictate the catalytic and photocatalytic efficacies of the systems.