Milliscale Self-Integration of Megamolecule Biopolymers on a Drying Gas–Aqueous Liquid Crystalline Interface

• Published in: Biomacromolecules Vol. 17; no. 6; pp. 2096 - 2103
• Main Authors: Okeyoshi, Kosuke, Okajima, Maiko K, Kaneko, Tatsuo
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 13.06.2016
• Subjects: Biopolymers - chemistry; Desiccation; Gases - chemistry; Liquid Crystals - chemistry; Microscopy, Polarization; Molecular Conformation; Molecular Weight; Particle Size; Phase Transition; Polysaccharides - chemistry; Polysaccharides, Bacterial - chemistry; Solutions; Water - chemistry
• ISSN: 1525-7797; 1526-4602
• DOI: 10.1021/acs.biomac.6b00302

A drying environment is always a proposition faced by dynamic living organisms using water, which are driven by biopolymer-based micro- and macrostructures. Here, we introduce a drying process for aqueous liquid crystalline (LC) solutions composed of biopolymer with extremely high molecular weight components such as polysaccharides, cytoskeletal proteins, and DNA. On controlling the mobility of the LC microdomain, the solutions showed milliscale self-integration starting from the unstable gas-LC interface during drying. In particular, we first identified giant rod-like microdomains (∼1 μm diameter and more than 20 μm length) of the mega-molecular polysaccharide, sacran, which is remarkably larger than other polysaccharides. These microdomains led to the formation of a single milliscale macrodomain on the interface. In addition, the dried polymer films on a solid substrate also revealed that such integration depends on the size of the microdomain. We envision that this simple drying method will be useful not only for understanding the biopolymer hierarchization at the macroscale level but also for preparation of surfaces with direction controllability, as seen in living organisms, for use in various fields such as diffusion, mechanics, and photonics.