We developed a dendritic molecular glue PC Glue-NBD that can serve universally to “turn on” protein–protein interactions (PPIs) spatiotemporally. PC Glue-NBD carrying multiple guanidinium ion (Gu + ) pendants can adhere strongly to target proteins and cover their surfaces including the PPI interface regions, thereby suppressing PPIs with their receptor proteins. Upon irradiation with UV light, PC Glue-NBD on a target protein is photocleaved at butyrate-substituted nitroveratryloxycarbonyl linkages in the dendrimer framework, so that the multivalency for the adhesion is reduced. Consequently, the guest protein is liberated and becomes eligible for a PPI. We found that hepatocyte growth factor HGF, when mixed with PC Glue-NBD, lost the affinity toward its receptor c-Met. However, upon exposure of the PC Glue-NBD/HGF hybrid to light-emitting diode light (365 nm), the PC Glue-NBD molecules on HGF were photocleaved as described above, so that HGF was liberated and retrieved its intrinsic PPI affinity toward c-Met. The turn-on PPI, thus achieved for HGF and c-Met, leads to cell migration, which can be made spatiotemporally with a millimeter-scale resolution by pointwise irradiation with UV light.
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Mogaki et al. (2019) studied this question.
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