Matthew G. Gold

This study shows that PKA can act as either an enzymatic or structural component depending on its anchoring site, using a SpyCatcher-SpyTag strategy to compare AKAP functions.

This study shows that CaMKII T305A/T306A mutations cause tight actinin binding and dendritic spine enlargement in unstimulated neurons, suggesting a structural role for CaMKII in LTP.

This study identifies how CaMKII and α-actinin-2 interactions drive dendritic spine enlargement during structural LTP by revealing molecular mechanisms and structural insights.

The paper shows homomeric Q/R edited AMPA receptors allow ion flow when desensitized, challenging the notion that desensitized channels are non-conducting.