دورية أكاديمية

Investigating the Impact of Hydrophobic Polymer Segments on the Self-Assembly Behavior of Supramolecular Cyclic Peptide Systems via Asymmetric-Flow Field Flow Fractionation.

التفاصيل البيبلوغرافية
العنوان: Investigating the Impact of Hydrophobic Polymer Segments on the Self-Assembly Behavior of Supramolecular Cyclic Peptide Systems via Asymmetric-Flow Field Flow Fractionation.
المؤلفون: Kariuki M; Department of Chemistry, University of Warwick, Coventry CV4 7AL, U.K., Rho JY; Department of Chemistry, University of Warwick, Coventry CV4 7AL, U.K., Hall SCL; ISIS Neutron and Muon Source, Rutherford Appleton Laboratory, Didcot OX11 0QX, U.K., Perrier S; Department of Chemistry, University of Warwick, Coventry CV4 7AL, U.K.; Warwick Medical School, University of Warwick, Coventry CV4 7AL, U.K.; Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Parkville, VIC 3052, Australia.
المصدر: Macromolecules [Macromolecules] 2023 Aug 26; Vol. 56 (17), pp. 6618-6632. Date of Electronic Publication: 2023 Aug 26 (Print Publication: 2023).
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: American Chemical Society Country of Publication: United States NLM ID: 0365316 Publication Model: eCollection Cited Medium: Print ISSN: 0024-9297 (Print) Linking ISSN: 00249297 NLM ISO Abbreviation: Macromolecules Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Washington, American Chemical Society.
مستخلص: The present study examines the behavior of cyclic peptide polymer conjugates that have been designed to combine their self-assembling ability via H-bonding with the properties of amphiphilic diblock copolymers. Using a combination of asymmetric flow-field flow fractionation (AF 4 ) and small-angle neutron scattering (SANS), we have uncovered unique insight based on the population of structures established at a 24 h equilibrium profile. Our results determine that by introducing a small quantity of hydrophobicity into the conjugated polymer corona, the resulting nanotube structures exhibit low unimer dissociation which signifies enhanced stability. Furthermore, as the hydrophobicity of the polymer corona is increased, the elongation of the nanotubes is observed due to an increase in the association of unimers. This encompasses not only the H-bonding of unimers into nanotubes but also the self-assembly of single nanotubes into segmented-nanotube structures with high aspect ratios. However, this influence relies on a subtle balance between the hydrophobicity and hydrophilicity of the polymer corona. This balance is proposed to determine the solvent entropic penalty of hydrating the system, whereby the cost scales with the hydrophobic quantity. Consequently, it has been suggested that at a critical hydrophobic quantity, the solvation penalty becomes high enough such that the self-assembly of the system deviates from ordered hydrogen bonding. The association behavior is instead dominated by the hydrophobic effect which results in the undesirable formation of disordered aggregates.
Competing Interests: The authors declare no competing financial interest.
(© 2023 The Authors. Published by American Chemical Society.)
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تواريخ الأحداث: Date Created: 20230918 Latest Revision: 20230921
رمز التحديث: 20230921
مُعرف محوري في PubMed: PMC10501196
DOI: 10.1021/acs.macromol.3c00442
PMID: 37720562
قاعدة البيانات: MEDLINE
الوصف
تدمد:0024-9297
DOI:10.1021/acs.macromol.3c00442