360028 Coacervate Driven Assemblies Using α-Helical Polypeptides

Thursday, November 20, 2014: 9:45 AM
International 7 (Marriott Marquis Atlanta)
Dimitrios Priftis1, Lorraine Leon1, Ziyuan Song2, Sarah L. Perry1, Khatcher O. Margossian1, Anna Tropnikova1, Jianjun Cheng3 and Matthew Tirrell1, (1)Institute for Molecular Engineering, University of Chicago, Chicago, IL, (2)Materials Science and Engineering, University of Illinois, Urbana, IL, (3)Materials Science and Engineering, University of Illinois, Urbana

A variety of materials with diverse structures and properties can form as a result of electrostatic interactions between oppositely charged macromolecules. Under defined conditions, complexation can lead to a phase separation phenomenon, referred to as complex coacervation. Using polypeptides, derived from amino acids, as a model system we identified the external parameters that affect coacervation,1 explored the thermodynamics of coacervate formation,2 and studied the rheological3 and interfacial properties4 of polypeptide coacervates. Here, we focus on the self-assembly of a different type of polypeptides. These water-soluble ultra-stable α-helical polypeptides are produced by elongating the charged side chains from the polypeptide backbone. Under similar conditions, mixing of these helical polypeptides with oppositely charged polyelectrolytes leads to the formation of liquid complexes (complex coacervates). Using the same strategy, coacervate core micelles are formed when the helical polypeptides are linked to a neutral hydrophilic block and are mixed with homopolymers of the opposite charge. The effects of salt, chirality and block length on both self-assembly structures will be discussed.

1. Priftis D., Tirrell M., Soft Mater 2012, 8, 9396-9405.                                                                                                

2. Priftis D., Laugel N., Tirrell M., Langmuir 2012, 28, 15947-15957.                                     

3. Priftis D., Megley K., Laugel N., Tirrell M., J. of Colloid and Interface Sci. 2013, 398, 39-50.                                

4. Priftis D., Farina R., Tirrell M., Langmuir 2012, 28, 8721-8729.


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See more of this Session: Charged and Ion-Containing Polymers
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