Inspired by biological systems, we report a supramolecular polymer-colloidal hydrogel (SPCH) composed of 98 wt % water that can be readily drawn into uniform (∼6-µm thick) "supramolecular fibers" at room temperature. Functionalized polymer-grafted silica nanoparticles, a semicrystalline hydroxyethyl cellulose derivative, and cucurbit[8]uril undergo aqueous self-assembly at multiple length scales to form the SPCH facilitated by host-guest interactions at the molecular level and nanofibril formation at colloidal-length scale. The fibers exhibit a unique combination of stiffness and high damping capacity (60-70%), the latter exceeding that of even biological silks and cellulose-based viscose rayon. The remarkable damping performance of the hierarchically structured fibers is proposed to arise from the complex combination and interactions of "hard" and "soft" phases within the SPCH and its constituents. SPCH represents a class of hybrid supramolecular composites, opening a window into fiber technology through low-energy manufacturing. supramolecular fiber | hydrogel | self-assembly | damping | spider silk I n nature, spiders spin silk fibers with superb properties at ambient temperatures and pressures (1, 2). We have yet to mimic such an elegant process. Conventionally, synthetic fibers are manufactured through a variety of spinning techniques, including wet, dry, gel, and electrospinning (3). Such approaches to generate fibers are limited by high energy input, laborious procedures, and intensive use of organic solvents. Supramolecular pathways enable the formation of filamentous soft materials that are showing promise in biomedical applications (4-6), such as cell culture (7-9) and tissue engineering (10). However, such materials are constrained by the length scale (submicrometer level) (11-13), energy intake during production (9), and complex design of assembly units (14).Here, we report drawing supramolecular fibers of arbitrary length from a dynamic supramolecular polymer-colloidal hydrogel (SPCH) at room temperature (Movie S1). The components consist of methyl viologen (MV)-functionalized polymer-grafted silica nanoparticles (P1), a semicrystalline polymer in the form of a hydroxyethyl cellulose derivative (H1), and cucurbit[8]uril (CB[8]) as illustrated in Fig. 1. The macrocycle CB[8] is capable of simultaneously encapsulating two guests within its cavity, forming a stable yet dynamic ternary complex, and has been exploited as a supramolecular "handcuff" to physical cross-link functional polymers (15-18). Introducing shape-persistent nanoparticles into the supramolecular hydrogel system allows for modification of the local gel structures at the colloidal-length scale, resulting in assemblies with unique emergent properties (19). The hierarchical nature of the SPCH is presented, where the hydrogel is composed of nanoscale fibrillar structures. The self-assembled SPCH composite exhibits great elasticity at a remarkably high water content (98%), showing a low-energy manufacturing process for fibers from natural, ...