Hofmeister Effects on Peptide Amphiphile Nanofiber Self-Assembly

Aysenur Iscen, George C. Schatz

Research output: Contribution to journalArticle

Abstract

Self-assembled peptide amphiphile (PA) nanofibers have emerged as bio-inspired materials with numerous applications in nanotechnology. However, environmental variables, such as salt concentration, pH, or temperature, can greatly impact the self-assembly process. Being able to tune the electrostatic interaction and intermolecular hydrogen bonding is essential in designing stable structures. The ion-specific effects on stabilization of peptides in solution typically follow the Hofmeister series and can be used to control the strength of interaction between ions and PAs. In this study, we performed atomistic molecular dynamics simulations to understand how we can use Hofmeister effects to control PA nanofiber structure. Our results show that the formation of β-sheets in PA nanofibers follows a direct Hofmeister order (F- > Cl- > Br- > I-), resulting from the strong interaction of strongly hydrated ions (F-, Cl-) with the charged amino acid residues on the nanofiber surface. On the other hand, weakly hydrated ions (I-, Br-) interact more preferably with the hydrophobic residues that form the stable β-sheets in the interior of the peptide closer to the core of the nanofiber. We also found that strongly hydrated ions can induce coil to β-sheet transition in the lysine residues close to the nanofiber surface by forming salt bridges between lysine residues of neighboring PA chains. With this work, we provide insight into how the structure of PA nanofibers can be tuned using different salt solutions for developing more stable supramolecular nanofibers for future applications.

Original languageEnglish
Pages (from-to)7006-7013
Number of pages8
JournalJournal of Physical Chemistry B
Volume123
Issue number32
DOIs
Publication statusPublished - Aug 15 2019

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Amphiphiles
Nanofibers
Self assembly
Peptides
peptides
self assembly
Ions
lysine
ions
salts
Salts
Lysine
nanotechnology
Coulomb interactions
amino acids
Nanotechnology
coils
stabilization
Molecular dynamics
Amino acids

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films
  • Materials Chemistry

Cite this

Hofmeister Effects on Peptide Amphiphile Nanofiber Self-Assembly. / Iscen, Aysenur; Schatz, George C.

In: Journal of Physical Chemistry B, Vol. 123, No. 32, 15.08.2019, p. 7006-7013.

Research output: Contribution to journalArticle

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