The DOI matches its Crossref record; 52 of the 52 references it cites were found in a registry or an index.
Self-reproducing catalyst drives repeated phospholipid synthesis and membrane growth
Open accessAbstract
Significance: We report on the design and synthesis of an artificial cell membrane that sustains continual growth. Lipid membranes are ubiquitous in all domains of life. Numerous studies have exploited the ability of lipids to self-assemble into bilayer vesicles with properties reminiscent of cellular membranes, but previous work has yet to mimic nature’s ability to support persistent phospholipid membrane formation. In this work, we have developed an artificial cell membrane that continually synthesizes all of the components needed to form additional catalytic membranes. These results demonstrate that complex lipid membranes capable of indefinite self-synthesis can emerge when supplied with simpler chemical building blocks.
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In the citing paper
“The model lipid catalyst has a headgroup constituting a hydrophilic chelator for Cu1+ ions and the hydrophobic moieties were three modified fatty acid chains. This amphiphilic molecule served as effective catalyst for the covalent bond formation between an alkyne-derivatized lysophospholipid and an azide-derivatized fatty acid analogue, leading to the formation of two-chain phospholipid analogue.”
From Systems protobiology: origin of life in lipid catalytic networks (2018) · cites this paper as [193]
In the citing paper
“The lipid-embodied network has four food compounds, three of which generate a lipid catalyst in two consecutive reactions.”
From Systems protobiology: origin of life in lipid catalytic networks (2018) · cites this paper as [193]
In the citing paper
“The experimental results provided are describable by a simple mutually catalytic network in line with the Kauffman–Hordijk model, as well as by the formalisms of M-GARD (previous section).”
From Systems protobiology: origin of life in lipid catalytic networks (2018) · cites this paper as [193]
In the citing paper
“The catalyst then enhances the rate of its own formation, as well as that of a reaction generating a two-chain phospholipid from a single chain phospholipid and a fatty acid analogue.”
From Systems protobiology: origin of life in lipid catalytic networks (2018) · cites this paper as [193]
In the citing paper
“but highlight a first published experimental instance of a simple lipid-based GARD network [193].”
From Systems protobiology: origin of life in lipid catalytic networks (2018) · cites this paper as [193]
In the citing paper
“Regarding evidence for our model's validity, we point out the insurmountable hurdles for comprehensive experimental verification, but highlight a first published experimental instance of a simple lipid-based GARD network [193].”
From Systems protobiology: origin of life in lipid catalytic networks (2018) · cites this paper as [193]
Citations
Cites
Cu-Catalyzed Azide−Alkyne Cycloaddition
Meldal, M., & Tornøe, C. W. (2008) · Chemical Reviews · doi:10.1021/cr0783479 · Cited by 4,780
Hydrogen Ion Buffers for Biological Research*
Good, N. E., Winget, G. D., Winter, W., Connolly, T. N., Izawa, S., & Singh, R. M. M. (1966) · Biochemistry · doi:10.1021/bi00866a011 · Cited by 2,762
Sinensky, M. (1974) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.71.2.522 · Cited by 1,551
Polytriazoles as Copper(I)-Stabilizing Ligands in Catalysis
Chan, T. R., Hilgraf, R., Sharpless, K. B., & Fokin, V. V. (2004) · Organic Letters · doi:10.1021/ol0493094 · Cited by 1,532
Experimental Models of Primitive Cellular Compartments: Encapsulation, Growth, and Division
Hanczyc, M. M., Fujikawa, S. M., & Szostak, J. W. (2003) · Science · doi:10.1126/science.1089904 · Cited by 848
Paula, S., Volkov, A. G., Van Hoek, A. N., Haines, T. H., & Deamer, D. W. (1996) · Biophysical Journal · doi:10.1016/s0006-3495(96)79575-9 · Cited by 578 · cited 1×
“The lack of a strong pH effect on the permeability coefficients of measured charged species supports a transient defect mechanism of membrane permeation over a solubility-diffusion mechanism (32).”
BackgroundLiposomes from ionic, single-chain amphiphiles
Hargreaves, W. R., & Deamer, D. W. (1978) · Biochemistry · doi:10.1021/bi00611a014 · Cited by 576
Kurihara, K., Tamura, M., Shohda, K.-I., Toyota, T., Suzuki, K., & Sugawara, T. (2011) · Nature Chemistry · doi:10.1038/nchem.1127 · Cited by 559
Coupled Growth and Division of Model Protocell Membranes
Zhu, T. F., & Szostak, J. W. (2009) · Journal of the American Chemical Society · doi:10.1021/ja900919c · Cited by 496
Acyl-CoA:Lysophospholipid Acyltransferases
Shindou, H., & Shimizu, T. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.r800046200 · Cited by 478
Adaptation of membrane lipids to alcohols
Ingram, L. O. (1976) · Journal of Bacteriology · doi:10.1128/jb.125.2.670-678.1976 · Cited by 476
Membrane damage by human islet amyloid polypeptide through fibril growth at the membrane
Engel, M. F., Khemtemourian, L., Kleijer, C. C., Meeldijk, H. J. D., Jacobs, J., Verkleij, A., de Kruijff, B., Killian, J., & Höppener, J. (2008) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0708354105 · Cited by 465
Autopoietic self-reproduction of fatty-acid vesicles
Walde, P., Wick, R., Fresta, M., Mangone, A., & Luisi, P. L. (1994) · Journal of the American Chemical Society · doi:10.1021/ja00105a004 · Cited by 444
The Emergence of Competition Between Model Protocells
Chen, I. A., Roberts, R. W., & Szostak, J. W. (2004) · Science · doi:10.1126/science.1100757 · Cited by 435
Compositional genomes: Prebiotic information transfer in mutually catalytic noncovalent assemblies
Segré, D., Ben-Eli, D., & Lancet, D. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.8.4112 · Cited by 398
Dynamics of transient pores in stretched vesicles
Sandre, O., Moreaux, L. C., & Brochard‐Wyart, F. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.19.10591 · Cited by 391
Competition between model protocells driven by an encapsulated catalyst
Adamala, K., & Szostak, J. W. (2013) · Nature Chemistry · doi:10.1038/nchem.1650 · Cited by 300
Life without a wall or division machine in Bacillus subtilis
Leaver, M., Domínguez-Cuevas, P., Coxhead, J. M., Daniel, R. A., & Errington, J. (2009) · Nature · doi:10.1038/nature07742 · Cited by 293
Physical effects underlying the transition from primitive to modern cell membranes
Budin, I., & Szostak, J. W. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100498108 · Cited by 289
Recent progress on acyl CoA: lysophospholipid acyltransferase research
Shindou, H., Hishikawa, D., 原山, 武., Yuki, K., & Shimizu, T. (2008) · Journal of Lipid Research · doi:10.1194/jlr.r800035-jlr200 · Cited by 286
Lateral compressibility of lipid mono- and bilayers. Theory of membrane permeability
Nagle, J. F., & Scott, H. L. (1978) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(78)90176-1 · Cited by 250
Achievements and open questions in the self-reproduction of vesicles and synthetic minimal cells
Stano, P., & Luisi, P. L. (2010) · Chemical Communications · doi:10.1039/b913997d · Cited by 224
Replicating vesicles as models of primitive cell growth and division
Hanczyc, M. M., & Szostak, J. W. (2004) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2004.10.002 · Cited by 221
Excess Membrane Synthesis Drives a Primitive Mode of Cell Proliferation
Mercier, R., Kawai, Y., & Errington, J. (2013) · Cell · doi:10.1016/j.cell.2013.01.043 · Cited by 220
Entrainment of a Population of Synthetic Genetic Oscillators
Mondragón-Palomino, O., Danino, T., Selimkhanov, J., Tsimring, L. S., & Hasty, J. (2011) · Science · doi:10.1126/science.1205369 · Cited by 190
Self-citationCoupling of the fusion and budding of giant phospholipid vesicles containing macromolecules
Terasawa, H., Nishimura, K., Suzuki, H., Matsuura, T., & Yomo, T. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120327109 · Cited by 183
Permeability of lipid bilayers to amino acids and phosphate
Chakrabarti, A. C., & Deamer, D. W. (1992) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(92)90308-9 · Cited by 158
Berclaz, N., Müller, M., Walde, P., & Luisi, P. L. (2000) · The Journal of Physical Chemistry B · doi:10.1021/jp001298i · Cited by 157
Light microscopic investigations of the autocatalytic self-reproduction of giant vesicles
Wick, R., Walde, P., & Luisi, P. L. (1995) · Journal of the American Chemical Society · doi:10.1021/ja00109a031 · Cited by 155
A Novel System of Self-Reproducing Giant Vesicles
Takakura, K., Toyota, T., & Sugawara, T. (2003) · Journal of the American Chemical Society · doi:10.1021/ja029379a · Cited by 146
Oscillatory phase separation in giant lipid vesicles induced by transmembrane osmotic differentials
Oglęcka, K., Rangamani, P., Liedberg, B., Kraut, R. S., & Parikh, A. N. (2014) · eLife · doi:10.7554/elife.03695 · Cited by 145
Thematic Review Series: Glycerolipids. Acyltransferases in bacterial glycerophospholipid synthesis
Zhang, Y., & Rock, C. O. (2008) · Journal of Lipid Research · doi:10.1194/jlr.r800005-jlr200 · Cited by 143
A giant step towards artificial life?
Deamer, D. W. (2005) · Trends in biotechnology · doi:10.1016/j.tibtech.2005.05.008 · Cited by 142
Minimal self-replicating systems
Robertson, A., Sinclair, A. J., & Philp, D. (2000) · Chemical Society Reviews · doi:10.1039/a803602k · Cited by 132
Micellar effects upon nucleophilic aromatic and aliphatic substitution
Bunton, C. A., & Robinson, L. (1968) · Journal of the American Chemical Society · doi:10.1021/ja01024a005 · Cited by 127
Membrane Assembly Driven by a Biomimetic Coupling Reaction
Budin, I., & Devaraj, N. K. (2011) · Journal of the American Chemical Society · doi:10.1021/ja2076873 · Cited by 122
Self-citationProton-hydroxide permeability of liposomes.
Deamer, D. W., & Nichols, J. L. (1983) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.80.1.165 · Cited by 121
Dissociation of Long and Very Long Chain Fatty Acids from Phospholipid Bilayers
Zhang, F., Kamp, F., & Hamilton, J. A. (1996) · Biochemistry · doi:10.1021/bi961685b · Cited by 112
Crucial Role for Membrane Fluidity in Proliferation of Primitive Cells
Mercier, R., Domínguez‐Cuevas, P., & Errington, J. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.03.008 · Cited by 105
Peterlin, P., Arrigler, V., Kogej, K., Svetina, S., & Walde, P. (2009) · Chemistry and Physics of Lipids · doi:10.1016/j.chemphyslip.2009.03.005 · Cited by 89
Preparation of Large Monodisperse Vesicles
Zhu, T. F., & Szostak, J. W. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005009 · Cited by 84
Vesicle Budding and the Origin of Cellular Life
Svetina, S. (2009) · ChemPhysChem · doi:10.1002/cphc.200900577 · Cited by 79
In Situ Vesicle Formation by Native Chemical Ligation
Brea, R. J., Cole, C. M., & Devaraj, N. K. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201408538 · Cited by 77
Self-citationTHE DIELECTRIC POLARIZATION OF LIQUIDS. X. THE POLARIZATION AND REFRACTION OF THE NORMAL PARAFFINS
Dornte, R. W., & Smyth, C. P. (1930) · Journal of the American Chemical Society · doi:10.1021/ja01372a009 · Cited by 67
Božič, B., & Svetina, S. (2004) · European Biophysics Journal · doi:10.1007/s00249-004-0404-5 · Cited by 60
Autocatalysis and organocatalysis with synthetic structures
Kamioka, S., Ajami, D., & REBEK, J. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912769107 · Cited by 60
Enzyme-containing liposomes can endogenously produce membrane-constituting lipids
Wick, R., & Luisi, P. L. (1996) · Chemistry & Biology · doi:10.1016/s1074-5521(96)90107-6 · Cited by 58
Bird, D. A., Laposata, M., & Hamilton, J. A. (1996) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)39129-x · Cited by 31
Suzuki, K., Toyota, T., Takakura, K., & Sugawara, T. (2009) · Chemistry Letters · doi:10.1246/cl.2009.1010 · Cited by 25
An enzymatically driven membrane reconstitution from solubilized components.
Deamer, D. W., & Boatman, D. E. (1980) · The Journal of Cell Biology · doi:10.1083/jcb.84.2.461 · Cited by 19
Jackson, W. G., Freasier, B. C., Goodyear, K., & Cooper, J. N. (2003) · Inorganica Chimica Acta · doi:10.1016/s0020-1693(03)00336-0 · Cited by 3
Rostovtsev, V. V., Green, L. G., Fokin, V. V., & Sharpless, K. B. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20020715)41:14
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Rideau, E., Dimova, R., Schwille, P., Wurm, F. R., & Landfester, K. (2018) · Chemical Society Reviews · doi:10.1039/c8cs00162f · Cited by 1,144
Artificial Cells: Synthetic Compartments with Life-like Functionality and Adaptivity
Buddingh’, B. C., & van Hest, J. C. M. (2017) · Accounts of Chemical Research · doi:10.1021/acs.accounts.6b00512 · Cited by 684
From dynamic self-assembly to networked chemical systems
Grzybowski, B. A., Fitzner, K., Paczesny, J., & Granick, S. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00089h · Cited by 306
Synthetic Cells: From Simple Bio‐Inspired Modules to Sophisticated Integrated Systems
Guindani, C., da Silva, L. C., Cao, S., Ivanov, T., & Landfester, K. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202110855 · Cited by 215
Artificial Cells: Past, Present and Future
Jiang, W., Wu, Z., Gao, Z., Wan, M., Zhou, M., Mao, C., & Shen, J. (2022) · ACS Nano · doi:10.1021/acsnano.2c06104 · Cited by 215
Metadata
- Authors
- Hardy, M. D., Yang, J., Selimkhanov, J., Cole, C. M., Tsimring, L. S., & Devaraj, N. K.
- Affiliations
- University of California San Diego (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2015-06-22
- Volume
- 112
- Issue
- 27
- Pages
- 8187-8192
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC4500204
- OpenAlex
- W1952600287
- Cited by
- 181
- References
- 52
- Citations by year
- 2026: 15 · 2025: 13 · 2024: 13 · 2023: 17 · 2022: 12 · 2021: 17 · 2020: 20 · 2019: 26 · 2018: 16 · 2017: 20 · 2016: 6 · 2015: 6
- FWCI
- 6.95
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Defense (W911NF-13-1-0383)
- National Science Foundation (CHE-1254611)
- HHS | National Institutes of Health (P50GM085764)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Lipid Membrane Structure and Behavior
- Physical Sciences › Physics and Astronomy › Astronomy and Astrophysics › Origins and Evolution of Life
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Keywords
- autocatalysis, phospholipid synthesis, model membranes, membrane growth, vesicle growth, membrane remodeling, biomimetic membranes, lipid bilayer formation, origin of life
- MeSH terms
- Catalysis, Cell Membrane, Copper, Lipid Bilayers, Membrane Lipids, Membranes, Artificial, Models, Chemical, Magnetic Resonance Spectroscopy, Phosphatidylcholines, Phospholipids, Triazoles, Molecular Structure, Microscopy, Confocal, Microscopy, Electron, Transmission, Unilamellar Liposomes, Time-Lapse Imaging, Cycloaddition Reaction
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