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Biology subjects

Chiang, Y.-W.

Publications and source records attributed to Chiang, Y.-W..

2 recordsLinked to original sources

An On-Demand Nanodisc Platform for Reconstitution of Functional Membrane Proteins into Model and Living Membranes

Membrane proteins are central to transport, signaling, and pharmacological regulation, yet their direct functional reconstitution into defined membrane environments remains technically challenging. Detergent-based workflows have enabled major advances in membrane protein research, but some applications require complementary strategies that better preserve native-like lipid environments. Cell-based expression approaches, meanwhile, require long incubation times and suffer from cell-type-dependent variability. Here, we establish nanodiscs as modular carriers for the rapid delivery of both lipids and full-length membrane proteins into model and cellular membranes. Using supported lipid bilayers, we first show that membrane scaffold protein (MSP) nanodiscs mediate efficient lipid transfer within minutes, with fluorescence recovery after photobleaching confirming lateral mobility of the delivered lipids. We then extend this strategy to the bacterial calcium channel BsYetJ, achieving concentration-dependent protein incorporation and single-molecule diffusion within supported lipid bilayers. Importantly, BsYetJ-loaded nanodiscs enable direct reconstitution of functional channels into intact mammalian plasma membranes across multiple cell lines. Calcium imaging demonstrates robust BsYetJ-mediated calcium influx, confirming that the delivered channel retains ion-conductive activity after transfer into heterologous cellular membranes. Crucially, this nanodisc-mediated delivery bypasses the variable trafficking pathways inherent to different host systems, allowing for the direct reconstitution of membrane proteins into target membranes while preserving their functional activity. Furthermore, unlike MSP nanodiscs, styrene-maleic acid (SMA) nanodiscs can directly capture membrane proteins from native cell membranes. This capability makes them particularly well-suited for studying complex and challenging membrane proteins. Therefore, we further generalize this platform using SMA nanodiscs . We demonstrate that, similar to MSP nanodiscs, SMA nanodiscs can efficiently deliver lipid cargo to supported bilayers and mammalian cells. By directly capturing full-length dopamine D2 receptor from cellular membranes and transferring it into naive target cells, we achieve functional GPCR reconstitution, as validated by specific binding of a custom fluorescent agonist. Together, these results demonstrate that nanodiscs can serve not only as stabilizing membrane mimetics but also as active delivery vehicles for on-demand membrane protein reconstitution. This approach provides a rapid and broadly applicable platform for interrogating ion channels, GPCRs, and other challenging pharmacological targets in user-defined membrane environments.

biochemistry↗

Nanodisc-Mediated Visualization of Crowding-Induced Condensation and Membrane Reorganization in Two-Dimensional Membrane Environments

Although biological membranes exhibit complex and dynamic organization, the mechanistic role of molecular crowding in governing lateral membrane heterogeneity remains poorly characterized experimentally. Here, we provide direct experimental visualization showing that crowding-induced condensation of membrane-anchored macromolecules above the bilayer interface reorganizes membrane dynamics and gives rise to spatially heterogeneous lipid mobility. Both PEGylated lipids and membrane-anchored proteins undergo surface-density-driven condensation on supported lipid bilayers, forming immobile regions that constrain lipid diffusion. Notably, the condensation threshold varies inversely with PEG chain length and surface density, defining a quantitative relationship between molecular size and crowding strength. To directly visualize these crowding-induced structures, we employed nanodelivery using lipid-loaded nanodiscs, revealing a clear correspondence between condensed crowder regions and diffusion barriers reminiscent of the picket-fence model of live-cell membranes. Similar condensation behavior observed for protein-crowded SLBs demonstrates the generality of this crowding-driven mechanism. Together, these findings establish surface-density-driven crowding and condensation of membrane-anchored macromolecules as a key physical mechanism underlying lateral membrane inhomogeneity and position nanodelivery as a general approach for interrogating membrane organization across synthetic and biological systems.

biophysics↗