Postsynaptic scaffold proteins immobilise neurotransmitter receptors in the synaptic membrane opposite to presynaptic vesicle release sites, thus ensuring efficient synaptic transmission. At inhibitory synapses in the spinal cord, the main scaffold protein gephyrin assembles in dense molecule clusters that provide binding sites for glycine receptors (GlyRs).Gephyrin and GlyRs can also interact outside of synapses where they form receptor-scaffold complexes. While several models for the formation of postsynaptic scaffold domains in the presence of receptor-scaffold interactions have been advanced, a clear picture of the coupled dynamics of receptors and scaffold proteins at synapses is lacking.To characterise the GlyR and gephyrin dynamics at inhibitory synapses we performed fluorescence time-lapse imaging after photoconversion in order to directly visualise the exchange kinetics of recombinant Dendra2-gephyrin in cultured spinal cord neurons.Immuno-immobilisation of endogenous GlyRs with specific antibodies abolished their lateral diffusion in the plasma membrane, as judged by the lack of fluorescence recovery after photobleaching. Moreover, the crosslinking of GlyRs significantly reduced the exchange of Dendra2-gephyrin compared to control conditions, suggesting that the kinetics of the synaptic gephyrin pool is strongly dependent on GlyR-gephyrin interactions. We did not observe any change in the total synaptic gephyrin levels after GlyR crosslinking, however, indicating that the number of gephyrin molecules at synapses is not primarily dependent on the exchange of GlyR-gephyrin complexes.We further show that our experimental data can be quantitatively accounted for by a model of receptor-scaffold dynamics that includes a tightly interacting receptor-scaffold domain, as well as more loosely bound receptor and scaffold populations that exchange with extrasynaptic pools. The model can make predictions for single molecule data such as typical dwell times of synaptic proteins. Taken together, our data demonstrate the reciprocal stabilisation of GlyRs and gephyrin at inhibitory synapses and provide a quantitative understanding of their dynamic organisation.

Postsynaptic scaffold proteins immobilise neurotransmitter receptors in the synaptic membrane opposite to presynaptic vesicle release sites, thus ensuring efficient synaptic transmission. At inhibitory synapses in the spinal cord, the main scaffold protein gephyrin assembles in dense molecule clusters that provide binding sites for glycine receptors (GlyRs). Gephyrin and GlyRs can also interact outside of synapses where they form receptor-scaffold complexes. While several models for the formation of postsynaptic scaffold domains in the presence of receptor-scaffold interactions have been advanced, a clear picture of the coupled dynamics of receptors and scaffold proteins at synapses is lacking.To characterise the GlyR and gephyrin dynamics at inhibitory synapses we performed fluorescence time-lapse imaging after photoconversion in order to directly visualise the exchange kinetics of recombinant Dendra2-gephyrin in cultured spinal cord neurons. Immuno-immobilisation of endogenous GlyRs with specific antibodies abolished their lateral diffusion in the plasma membrane, as judged by the lack of fluorescence recovery after photobleaching. Moreover, the crosslinking of GlyRs significantly reduced the exchange of Dendra2-gephyrin compared to control conditions, suggesting that the kinetics of the synaptic gephyrin pool is strongly dependent on GlyR-gephyrin interactions. We did not observe any change in the total synaptic gephyrin levels after GlyR crosslinking, however, indicating that the number of gephyrin molecules at synapses is not primarily dependent on the exchange of GlyR-gephyrin complexes.We further show that our experimental data can be quantitatively accounted for by a model of receptor-scaffold dynamics that includes a tightly interacting receptor-scaffold domain, as well as more loosely bound receptor and scaffold populations that exchange with extrasynaptic pools. The model can make predictions for single molecule data such as typical dwell times of synaptic proteins. Taken together, our data demonstrate the reciprocal stabilisation of GlyRs and gephyrin at inhibitory synapses and provide a quantitative understanding of their dynamic organisation.Statement of significanceThe efficiency of signal transmission between neurons depends strongly on the number of available neurotransmitter receptors in the postsynaptic membrane. Postsynaptic scaffold proteins provide binding sites for receptors, thus setting the gain of synaptic transmission. However, the importance of receptor-scaffold interactions for the stability of the postsynaptic scaffold itself has received relatively little attention. Using time-lapse imaging of glycine receptors and gephyrin scaffolds at inhibitory synapses in spinal cord neurons together with biophysical modelling, we show that receptor mobility controls the exchange but not the total number of gephyrin molecules at the synapse, and predict that glycine receptors and gephyrin scaffolds dynamically organise into different subpopulations with varying degrees of reciprocal stabilisation.