TY - JOUR
T1 - Self-Assembly of Tunable Intrinsically Disordered Peptide Amphiphiles
AU - Ehm, Tamara
AU - Shinar, Hila
AU - Jacoby, Guy
AU - Meir, Sagi
AU - Koren, Gil
AU - Segal Asher, Merav
AU - Korpanty, Joanna
AU - Thompson, Matthew P.
AU - Gianneschi, Nathan C.
AU - Kozlov, Michael M.
AU - Azoulay-Ginsburg, Salome
AU - Amir, Roey J.
AU - Rädler, Joachim O.
AU - Beck, Roy
N1 - Publisher Copyright:
© 2022 American Chemical Society.
PY - 2023/1/9
Y1 - 2023/1/9
N2 - Intrinsically disordered peptide amphiphiles (IDPAs) present a novel class of synthetic conjugates that consist of short hydrophilic polypeptides anchored to hydrocarbon chains. These hybrid polymer-lipid block constructs spontaneously self-assemble into dispersed nanoscopic aggregates or ordered mesophases in aqueous solution due to hydrophobic interactions. Yet, the possible sequence variations and their influence on the self-assembly structures are vast and have hardly been explored. Here, we measure the nanoscopic self-assembled structures of four IDPA systems that differ by their amino acid sequence. We show that permutations in the charge pattern along the sequence remarkably alter the headgroup conformation and consequently alter the pH-triggered phase transitions between spherical, cylindrical micelles and hexagonal condensed phases. We demonstrate that even a single amino acid mutation is sufficient to tune structural transitions in the condensed IDPA mesophases, while peptide conformations remain unfolded and disordered. Furthermore, alteration of the peptide sequence can render IDPAs to become susceptible to enzymatic cleavage and induce enzymatically activated phase transitions. These results hold great potential for embedding multiple functionalities into lipid nanoparticle delivery systems by incorporating IDPAs with the desired properties.
AB - Intrinsically disordered peptide amphiphiles (IDPAs) present a novel class of synthetic conjugates that consist of short hydrophilic polypeptides anchored to hydrocarbon chains. These hybrid polymer-lipid block constructs spontaneously self-assemble into dispersed nanoscopic aggregates or ordered mesophases in aqueous solution due to hydrophobic interactions. Yet, the possible sequence variations and their influence on the self-assembly structures are vast and have hardly been explored. Here, we measure the nanoscopic self-assembled structures of four IDPA systems that differ by their amino acid sequence. We show that permutations in the charge pattern along the sequence remarkably alter the headgroup conformation and consequently alter the pH-triggered phase transitions between spherical, cylindrical micelles and hexagonal condensed phases. We demonstrate that even a single amino acid mutation is sufficient to tune structural transitions in the condensed IDPA mesophases, while peptide conformations remain unfolded and disordered. Furthermore, alteration of the peptide sequence can render IDPAs to become susceptible to enzymatic cleavage and induce enzymatically activated phase transitions. These results hold great potential for embedding multiple functionalities into lipid nanoparticle delivery systems by incorporating IDPAs with the desired properties.
UR - http://www.scopus.com/inward/record.url?scp=85143613119&partnerID=8YFLogxK
U2 - 10.1021/acs.biomac.2c00866
DO - 10.1021/acs.biomac.2c00866
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C2 - 36469950
AN - SCOPUS:85143613119
SN - 1525-7797
VL - 24
SP - 98
EP - 108
JO - Biomacromolecules
JF - Biomacromolecules
IS - 1
ER -