Salt- and pH-Triggered Helix-Coil Transition of Ionic Polypeptides under Physiology Conditions.

Controlling the helix-coil transition of polypeptides under physiological conditions is an attractive way toward smart functional materials. Here, we report the synthesis of a series of tertiary amine-functionalized ethylene glycol (EG(x))-linked polypeptide electrolytes with their secondary structures tunable under physiological conditions. The resultant polymers, denoted as P(EG(x)DMA-Glu) (x = 1, 2, and 3), show excellent aqueous solubility (>20 mg/mL) regardless of their charge states. Unlike poly-L-lysine that can form a helix only at pH above 10, P(EG(x)DMA-Glu) undergo a pH-dependent helix-coil switch with their transition points within the physiological range (pH similar to 5.3-6.5). Meanwhile, P(EG(x)DMA-Glu) exhibit an unusual salt-induced helical conformation presumably owing to the unique properties of EG(x) linkers. Together, the current work highlights the importance of fine-tuning the linker chemistry in achieving conformation-switchable polypeptides and represents a facile approach toward stimuli-responsive biopolymers for advanced biological applications.