TY - JOUR
T1 - Lipid Vesicle-Coated Complex Coacervates
AU - Pir Cakmak, Fatma
AU - Grigas, Alex T.
AU - Keating, Christine D.
N1 - Funding Information:
*E-mail: keating@chem.psu.edu. ORCID Christine D. Keating: 0000-0001-6039-1961 Present Address †Program in Computational Biology and Bioinformatics, Yale University, New Haven, Connecticut 06520, United States (A.T.G.). Author Contributions F.P.C. and A.T.G. performed the experiments. F.P.C. and C.D.K. conceived and designed the experiments and analyzed the data. F.P.C. and C.D.K. wrote the paper, with contributions from A.T.G. Funding This work was primarily supported by the NASA Exobiology program, grant 80NSSC17K0034, with additional support from the National Science Foundation grant CHE-1844313 RoL: RAISE: DESYN-C3. Undergraduate researcher A.T.G. was supported by an award from the Penn State University Eberly College of Science and by a Rodney A. Erickson Discovery Grant. Notes The authors declare no competing financial interest.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/6/18
Y1 - 2019/6/18
N2 - Compartmentalization by complex coacervation is important across a range of different fields including subcellular and prebiotic organization, biomedicine, food science, and personal care products. Often, lipid self-assemblies such as vesicles are also present intracellularly or in commercial formulations. A systematic understanding of how phospholipid vesicles interact with different complex coacervates could provide insight and improve control over these systems. In this manuscript, anionic phospholipid vesicles were added to a series of different complex coacervate samples in which coacervates were formed by mixing one of five polycations with one of three (poly)anions that varied in chemical structure and length. Vesicles were found to assemble at the coacervate/continuous phase interface and/or form aggregates. We report how factors such as the charge density of polyelectrolytes and the charge ratio of cationic-to-anionic moieties impact the vesicle distribution in coacervate samples. Our findings emphasize the importance of interactions between vesicles and polycations in the dilute supernatant phase for determining whether the vesicles aggregate prior to assembly at the liquid-liquid interface. The uptake of an RNA oligonucleotide (A15) was also investigated to understand the effect of these liposome coatings on diffusion into coacervate droplets. Systems in which uniform vesicle coronas assemble around coacervate droplets without restricting the entry of biomolecules such as RNAs could be of interest as bioreactors.
AB - Compartmentalization by complex coacervation is important across a range of different fields including subcellular and prebiotic organization, biomedicine, food science, and personal care products. Often, lipid self-assemblies such as vesicles are also present intracellularly or in commercial formulations. A systematic understanding of how phospholipid vesicles interact with different complex coacervates could provide insight and improve control over these systems. In this manuscript, anionic phospholipid vesicles were added to a series of different complex coacervate samples in which coacervates were formed by mixing one of five polycations with one of three (poly)anions that varied in chemical structure and length. Vesicles were found to assemble at the coacervate/continuous phase interface and/or form aggregates. We report how factors such as the charge density of polyelectrolytes and the charge ratio of cationic-to-anionic moieties impact the vesicle distribution in coacervate samples. Our findings emphasize the importance of interactions between vesicles and polycations in the dilute supernatant phase for determining whether the vesicles aggregate prior to assembly at the liquid-liquid interface. The uptake of an RNA oligonucleotide (A15) was also investigated to understand the effect of these liposome coatings on diffusion into coacervate droplets. Systems in which uniform vesicle coronas assemble around coacervate droplets without restricting the entry of biomolecules such as RNAs could be of interest as bioreactors.
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U2 - 10.1021/acs.langmuir.9b00213
DO - 10.1021/acs.langmuir.9b00213
M3 - Article
C2 - 31091880
AN - SCOPUS:85066399327
SN - 0743-7463
VL - 35
SP - 7830
EP - 7840
JO - Langmuir
JF - Langmuir
IS - 24
ER -