Thermostable cross-β structures are characteristic of pathological amyloid fibrils, but these structures cannot explain the reversible nature of fibrils formed by RNA-binding proteins such as fused in sarcoma (FUS), involved in RNA granule assembly. Here, we find that two tandem (S/G)Y(S/G) motifs of the human FUS low-complexity domain (FUS LC) form reversible fibrils in a temperature- and phosphorylation-dependent manner. We named these motifs reversible amyloid cores, or RAC1 and RAC2, and determined their atomic structures in fibrillar forms, using microelectron and X-ray diffraction techniques. The RAC1 structure features an ordered-coil fibril spine rather than the extended β-strand typical of amyloids. Ser42, a phosphorylation site of FUS, is critical in the maintenance of the ordered-coil structure, which explains how phosphorylation controls fibril formation. The RAC2 structure shows a labile fibril spine with a wet interface. These structures illuminate the mechanism of reversible fibril formation and dynamic assembly of RNA granules.

A simple strategy is provided to construct novel supramolecular hydrogels with both self-healing and shape memory properties. Starting from achieving self-healable hydrogel based on the dynamic interactions of phenylboronic acid modified sodium alginate (Alg-PBA) and poly(vinyl alcohol) (PVA), further formation of a complex of alginate with Ca(2+) renders this hydrogel with the capability of shape memory at the macro-/microscopic scales.

A robust and simple method is provided to fabricate Janus polymer/carbon nanotube (CNT) hybrid membranes for oil/water separation. Starting from CNT membranes formed by dispensing, hydrophobic poly(styrene) (PS) and hydrophilic poly(N,N-dimethylaminoethyl methacrylate) (PDMAEMA) were grated from different sides of the photoactive CNT membranes via self-initiated photografting and photopolymerization (SIPGP) to achieve Janus polymer/CNTs hybrid membranes. The obtained membranes have excellent oil/water selectivity in the removal of oil from water. Moreover, they can effectively separate both surfactant-stabilized oil-in-water and water-in-oil emulsions because of the anisotropic wettability of the membranes.