Polymer–Surfactant Driven Interactions and the Resultant Microstructure in Protein-Containing Liquid Crystal Droplets
Integration of molecular liquid crystals (LCs) with functional proteins can provide new class of materials for potential applications in optical biosensing. However, hydrophobic nematic LCs (length ∼ 1–2 nm) and hydrophilic proteins, size ∼ O (nm), do not intermix without chemical modification of at...
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Published in: | Langmuir Vol. 37; no. 41; pp. 11949 - 11960 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
American Chemical Society
19-10-2021
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Online Access: | Get full text |
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Summary: | Integration of molecular liquid crystals (LCs) with functional proteins can provide new class of materials for potential applications in optical biosensing. However, hydrophobic nematic LCs (length ∼ 1–2 nm) and hydrophilic proteins, size ∼ O (nm), do not intermix without chemical modification of at least one of them. Bioconjugation of proteins with a polyethylene glycol-based polymeric surfactant (PS) can provide a core–shell system that is sequestered within nonaqueous LC (4-cyano-4′-pentylbiphenyl) microdroplets. However, the nature of interactions between the components and detailed understanding of the resultant hybrid microstructure remains unclear. Here, using a combination of isothermal titration calorimetry (ITC), fluorescence microscopy, and infrared-imaging spectroscopy, we show that strong hydrophobic interactions between the LC and PS drives the sequestration of a myoglobin–PS (Mb–PS; dispersed in the aqueous phase) into the LC spherical microdroplets or even into a bulk LC phase. The average values of both, the binding constant and the standard molar enthalpy change, are increased by approximately a factor of 2.5 times when the unmodified Mb is conjugated to the PS. Small-angle X-ray scattering studies reveal that LC molecules act as a solvent for the Mb–PS conjugate; furthermore, the LC long-range order is disturbed due to mixing, as exemplified by the change in its coherence length from 8.9 to 5.7 nm. Detailed all-atomistic molecular dynamic simulations for a three-component PS–water–LC system show a change in interaction energy of −144 kJ mol–1 PS–1 upon the contact of PS chains (initially dispersed in water) with LC and agree with the ITC experiments. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0743-7463 1520-5827 |
DOI: | 10.1021/acs.langmuir.1c00960 |