Oppositely charged biomolecules can coassemble into functional units. For example, actin-binding protein complexes have been shown to coassemble into cytoskeleton components,
and cationic-anionic co-assembled peptide amphiphiles have been shown to co-assemble into functional nanofibers. Cationic-anionic co-assemblies have surface charge heterogeneities that result from the delicate balance between electrostatics and packing constraints. Researchers at the NU-MRSEC studying the interaction among assemblies with surface charged heterogeneities have found that attractions among fibers appear as a result of correlations and polarization of surface charged domains. These results reveal the importance of charge heterogeneities in cationic-anionic co-assemblies of complex molecules and suggest a promising strategy for the fabrication of assemblies with predictable surface charge patterns for developing functional biomolecular assemblies.
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