Instabilities of Charged Polyampholytes

Abstract

We consider polymers formed from a (quenched) random sequence of charged monomers of opposite signs. Such polymers, known as polyampholytes (PAs), are compact when completely neutral and expanded when highly charged. We examine the transition between the two regimes by Monte Carlo simulations, and by analogies to charged drops. We find that the overall excess charge, Q, is the main determinant of the size of the PA. A polymer composed of N charges of q0 is compact for Q<Qc≈ q0 N, and expanded otherwise. The transition is reminiscent of the Rayleigh shape instability of a charged drop. A uniform excess charge causes the breakup of a fluid drop, and stretches out a polymer to a necklace shape. The inhomogeneities in charge distort the shape away from an ordered necklace.

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