Cited by 13Origins and Evolution of LifeEvolution and Genetic DynamicsRNA and protein synthesis mechanisms

Replication of Simulated Prebiotic Amphiphilic Vesicles in a Finite Environment Exhibits Complex Behavior That Includes High Progeny Variability and Competition

Open access
Armstrong, Don L., Lancet, Doron, Zidovetzki, Raphael·2018·Astrobiology

Abstract

We studied the simulated replication and growth of prebiotic vesicles composed of 140 phospholipids and cholesterol using our R-GARD (Real Graded Autocatalysis Replication Domain) formalism that utilizes currently extant lipids that have known rate constants of lipid-vesicle interactions from published experimental data. R-GARD normally modifies kinetic parameters of lipid-vesicle interactions based on vesicle composition and properties. Our original R-GARD model tracked the growth and division of one vesicle at a time in an environment with unlimited lipids at a constant concentration. We explore here a modified model where vesicles compete for a finite supply of lipids. We observed that vesicles exhibit complex behavior including initial fast unrestricted growth, followed by intervesicle competition for diminishing resources, then a second growth burst driven by better-adapted vesicles, and ending with a final steady state. Furthermore, in simulations without kinetic parameter modifications ("invariant kinetics"), the initial replication was an order of magnitude slower, and vesicles' composition variability at the final steady state was much lower. The complex kinetic behavior was not observed either in the previously published R-GARD simulations or in additional simulations presented here with only one lipid component. This demonstrates that both a finite environment (inducing selection) and multiple components (providing variation for selection to act upon) are crucial for portraying evolution-like behavior. Such properties can improve survival in a changing environment by increasing the ability of early protocellular entities to respond to rapid environmental fluctuations likely present during abiogenesis both on Earth and possibly on other planets. This in silico simulation predicts that a relatively simple in vitro chemical system containing only lipid molecules might exhibit properties that are relevant to prebiotic processes. Key Words: Phospholipid vesicles-Prebiotic compartments-Prebiotic vesicle competition-Prebiotic vesicle variability. Astrobiology 18, 419-430.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1089/ast.2016.1615

Cites

14 of 14 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • GARD is much less abstract than many other models for life's origin because it uses rigorous chemical kinetic equations, and it is the only model in its genre that uses experiment-based graded catalytic parameters and in two papers also the properties of real lipid molecules.

    “This is wrong: in using rigorous chemical kinetic equations, GARD is much less abstract than many other models for life's origin. Further, it is the only model in its genre that uses experiment-based graded catalytic parameters (§4) and in two papers also the properties of real lipid molecules [60,119].”

    From Systems protobiology: origin of life in lipid catalytic networks (2018) · cites this paper as [119]

    Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.

    Experimental — accuracy not yet measured
  • In R-GARD simulations with a finite supply of amphiphiles, complex kinetic behaviour including inter-assembly competition was transiently observed.

    “In such simulations, we were able to transiently observe complex kinetic behaviour, including inter-assembly competition.”

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 29

  1. Adamala K. and Szostak J.W. (2013) Competition between model protocells driven by an encapsulated catalyst. Nat Chem 5: 495– 501 23695631 PMC4041014
  2. Armstrong D.L., Markovitch O., Zidovetzki R., and Lancet D. (2011) Replication of simulated prebiotic amphiphile vesicles controlled by experimental lipid physicochemical properties. Phys Biol 8, doi: 10.1088/1478-3975/8/6/066001 21946049 · DOI · Paper page
  3. Blain J.C. and Szostak J.W. (2014) Progress toward synthetic cells. Annu Rev Biochem 83: 615– 640 24606140
  4. Božič B. and Svetina S. (2004) A relationship between membrane properties forms the basis of a selectivity mechanism for vesicle self-reproduction. Eur Biophys J 33: 565– 571 15095026
  5. Božič B. and Svetina S. (2007) Vesicle self-reproduction: the involvement of membrane hydraulic and solute permeabilities. Eur Phys J E Soft Matter 24: 79– 90 17882352
  6. Budin I. and Szostak J.W. (2011) Physical effects underlying the transition from primitive to modern cell membranes. Proc Natl Acad Sci USA 108: 5249– 5254 21402937 PMC3069173
  7. Cronin J.R. (1998) Clues from the origin of the Solar System: meteorites. In The Molecular Origin of Life: Assembling Pieces of the Puzzle, edited by Andre B., Cambridge University Press, Cambridge, UK, pp 119– 146
  8. Damer B. (2016) A field trip to the Archaean in search of Darwin's warm little pond. Life (Basel) 6, doi: 10.3390/life6020021 PMC4931458 27231942 · DOI
  9. Fellermann H. and Solé R.V. (2007) Minimal model of self-replicating nanocells: a physically embodied information-free scenario. Philos Trans R Soc Lond B Biol Sci 362: 1803– 1811 17510020 PMC2442394
  10. Georgiou C.D. and Deamer D.W. (2014) Lipids as universal biomarkers of extraterrestrial life. Astrobiology 14: 541– 549 24735484
  11. Hanczyc M.M., Fujikawa S.M., and Szostak J.W. (2003) Experimental models of primitive cellular compartments: encapsulation, growth, and division. Science 302: 618– 622 14576428 PMC4484575
  12. Hargreaves W.R., Mulvihill S.J., and Deamer D.W. (1977) Synthesis of phophospholipids and membranes in prebiotic conditions. Nature 266: 78– 80 840303
  13. Mavelli F. and Ruiz-Mirazo K. (2010) ENVIRONMENT: a computational platform to stochastically simulate reacting and self-reproducing lipid compartments. Phys Biol 7, doi: 10.1088/1478-3975/7/3/036002 20702920 · DOI
  14. McCollom T.M., Ritter G., and Simoneit B.R. (1999) Lipid synthesis under hydrothermal conditions by Fischer-Tropsch-type reactions. Orig Life Evol Biosph 29: 153– 166 10227201
  15. Patel B.H., Percivalle C., Ritson D.J., Duffy C.D., and Sutherland J.D. (2015) Common origins of RNA, protein and lipid precursors in a cyanosulfidic protometabolism. Nat Chem 7: 301– 307 25803468 PMC4568310
  16. Pekkonen M., Ketola T., and Laakso J.T. (2013) Resource availability and competition shape the evolution of survival and growth ability in a bacterial community. PLoS One 8, doi: 10.1371/journal.pone.0076471 PMC3787024 24098791 · DOI
  17. Pohorille A. and Deamer D. (2009) Self-assembly and function of primitive cell membranes. Res Microbiol 160: 449– 456 19580865
  18. Pulselli R.M., Simoncini E., and Tiezzi E. (2009) Self-organization in dissipative structures: a thermodynamic theory for the emergence of prebiotic cells and their epigenetic evolution. Biosystems 3: 237– 241 19758548
  19. Regis E. (2009) What is Life? Investigating the Nature of Life in the Age of Synthetic Biology, Oxford University Press, Oxford, UK
  20. Schrum J.P., Zhu T.F., and Szostak J.W. (2010) The origins of cellular life. Cold Spring Harb Perspect Biol 2, doi: 10.1101/cshperspect.a002212 PMC2926753 20484387 · DOI · Paper page
  21. Shenhav B., Bar-Even A., Kafri R., and Lancet D. (2005) Polymer GARD: computer simulation of covalent bond formation in reproducing molecular assemblies. Orig Life Evol Biosph 35: 111– 133 16010993
  22. Shirt-Ediss B., Ruiz-Mirazo K., Mavelli F., and Solé R.V. (2014) Modelling lipid competition dynamics in heterogeneous protocell populations. Sci Rep 4, doi: 10.1038/srep05675 PMC4097352 25024020 · DOI
  23. Svetina S. (2012) Cellular life could have emerged from properties of vesicles. Orig Life Evol Biosph 42: 483– 486 23073647
  24. Szostak J.W. (2011) An optimal degree of physical and chemical heterogeneity for the origin of life? Philos Trans R Soc Lond B Biol Sci 366: 2894– 2901 21930580 PMC3158921
  25. Takakura K., Toyota T., and Sugawara T. (2003) A novel system of self-reproducing giant vesicles. J Am Chem Soc 125: 8134– 8140 12837083
  26. Takakura K., Toyota T., and Sugawara T. (2004) A novel system of self-reproducing giant vesicles. J Am Chem Soc 125: 8134– 8140 12837083
  27. Thomas J.A. and Rana F.R. (2007) The influence of environmental conditions, lipid composition, and phase behavior on the origin of cell membranes. Orig Life Evol Biosph 37: 267– 285 17361322
  28. Toyota T., Takakura K., Kageyama Y., Kurihara K., Maru N., Ohnuma K., Kaneko K., and Sugawara T. (2008) Population study of sizes and components of self-reproducing giant multilamellar vesicles. Langmuir 24: 3037– 3044 18278955
  29. Zhu T.F. and Szostak J.W. (2009) Coupled growth and division of model protocell membranes. J Am Chem Soc 131: 5705– 5713 19323552 PMC2669828

Cited by

Sorted by citations

Authors
Armstrong, D. L., Lancet, D., & Zidovetzki, R.
Affiliations
  • University of California, Riverside (US)
  • Weizmann Institute of Science (IL)
Corresponding author
Zidovetzki, Raphael
Venue
Astrobiology
Published
2018-04
Volume
18
Issue
4
Pages
419-430
ISSN
  • 1531-1074 (ISSN-L)
  • 1557-8070
OpenAlex
W2795159781
Cited by
13
References
14
Citations by year
2026: 1 · 2025: 1 · 2024: 4 · 2023: 1 · 2021: 2 · 2020: 1 · 2019: 2 · 2018: 1
FWCI
0.80
Type
journal article
Language
en
Open access
Locations
  • Astrobiology (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion, other-oa)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
Weizmann Institute of Science
Topics
  • Physical Sciences › Physics and Astronomy › Astronomy and Astrophysics › Origins and Evolution of Life
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
Keywords
phospholipid vesicles, protocells, origin of life, selection, computer simulation, cholesterol
MeSH terms
Computer Simulation, Environment, Kinetics, Lipids, Models, Chemical, Earth, Planet

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review