Cargando…
Physical Routes to Primitive Cells: An Experimental Model Based on the Spontaneous Entrapment of Enzymes inside Micrometer-Sized Liposomes
How did primitive living cells originate? The formation of early cells, which were probably solute-filled vesicles capable of performing a rudimentary metabolism (and possibly self-reproduction), is still one of the big unsolved questions in origin of life. We have recently used lipid vesicles (lipo...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390888/ https://www.ncbi.nlm.nih.gov/pubmed/25793278 http://dx.doi.org/10.3390/life5010969 |
_version_ | 1782365746023628800 |
---|---|
author | D’Aguanno, Erica Altamura, Emiliano Mavelli, Fabio Fahr, Alfred Stano, Pasquale Luisi, Pier Luigi |
author_facet | D’Aguanno, Erica Altamura, Emiliano Mavelli, Fabio Fahr, Alfred Stano, Pasquale Luisi, Pier Luigi |
author_sort | D’Aguanno, Erica |
collection | PubMed |
description | How did primitive living cells originate? The formation of early cells, which were probably solute-filled vesicles capable of performing a rudimentary metabolism (and possibly self-reproduction), is still one of the big unsolved questions in origin of life. We have recently used lipid vesicles (liposomes) as primitive cell models, aiming at the study of the physical mechanisms for macromolecules encapsulation. We have reported that proteins and ribosomes can be encapsulated very efficiently, against statistical expectations, inside a small number of liposomes. Moreover the transcription-translation mixture, which realistically mimics a sort of minimal metabolic network, can be functionally reconstituted in liposomes owing to a self-concentration mechanism. Here we firstly summarize the recent advancements in this research line, highlighting how these results open a new vista on the phenomena that could have been important for the formation of functional primitive cells. Then, we present new evidences on the non-random entrapment of macromolecules (proteins, dextrans) in phospholipid vesicle, and in particular we show how enzymatic reactions can be accelerated because of the enhancement of their concentration inside liposomes. |
format | Online Article Text |
id | pubmed-4390888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-43908882015-05-21 Physical Routes to Primitive Cells: An Experimental Model Based on the Spontaneous Entrapment of Enzymes inside Micrometer-Sized Liposomes D’Aguanno, Erica Altamura, Emiliano Mavelli, Fabio Fahr, Alfred Stano, Pasquale Luisi, Pier Luigi Life (Basel) Article How did primitive living cells originate? The formation of early cells, which were probably solute-filled vesicles capable of performing a rudimentary metabolism (and possibly self-reproduction), is still one of the big unsolved questions in origin of life. We have recently used lipid vesicles (liposomes) as primitive cell models, aiming at the study of the physical mechanisms for macromolecules encapsulation. We have reported that proteins and ribosomes can be encapsulated very efficiently, against statistical expectations, inside a small number of liposomes. Moreover the transcription-translation mixture, which realistically mimics a sort of minimal metabolic network, can be functionally reconstituted in liposomes owing to a self-concentration mechanism. Here we firstly summarize the recent advancements in this research line, highlighting how these results open a new vista on the phenomena that could have been important for the formation of functional primitive cells. Then, we present new evidences on the non-random entrapment of macromolecules (proteins, dextrans) in phospholipid vesicle, and in particular we show how enzymatic reactions can be accelerated because of the enhancement of their concentration inside liposomes. MDPI 2015-03-18 /pmc/articles/PMC4390888/ /pubmed/25793278 http://dx.doi.org/10.3390/life5010969 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article D’Aguanno, Erica Altamura, Emiliano Mavelli, Fabio Fahr, Alfred Stano, Pasquale Luisi, Pier Luigi Physical Routes to Primitive Cells: An Experimental Model Based on the Spontaneous Entrapment of Enzymes inside Micrometer-Sized Liposomes |
title | Physical Routes to Primitive Cells: An Experimental Model Based on the Spontaneous Entrapment of Enzymes inside Micrometer-Sized Liposomes |
title_full | Physical Routes to Primitive Cells: An Experimental Model Based on the Spontaneous Entrapment of Enzymes inside Micrometer-Sized Liposomes |
title_fullStr | Physical Routes to Primitive Cells: An Experimental Model Based on the Spontaneous Entrapment of Enzymes inside Micrometer-Sized Liposomes |
title_full_unstemmed | Physical Routes to Primitive Cells: An Experimental Model Based on the Spontaneous Entrapment of Enzymes inside Micrometer-Sized Liposomes |
title_short | Physical Routes to Primitive Cells: An Experimental Model Based on the Spontaneous Entrapment of Enzymes inside Micrometer-Sized Liposomes |
title_sort | physical routes to primitive cells: an experimental model based on the spontaneous entrapment of enzymes inside micrometer-sized liposomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390888/ https://www.ncbi.nlm.nih.gov/pubmed/25793278 http://dx.doi.org/10.3390/life5010969 |
work_keys_str_mv | AT daguannoerica physicalroutestoprimitivecellsanexperimentalmodelbasedonthespontaneousentrapmentofenzymesinsidemicrometersizedliposomes AT altamuraemiliano physicalroutestoprimitivecellsanexperimentalmodelbasedonthespontaneousentrapmentofenzymesinsidemicrometersizedliposomes AT mavellifabio physicalroutestoprimitivecellsanexperimentalmodelbasedonthespontaneousentrapmentofenzymesinsidemicrometersizedliposomes AT fahralfred physicalroutestoprimitivecellsanexperimentalmodelbasedonthespontaneousentrapmentofenzymesinsidemicrometersizedliposomes AT stanopasquale physicalroutestoprimitivecellsanexperimentalmodelbasedonthespontaneousentrapmentofenzymesinsidemicrometersizedliposomes AT luisipierluigi physicalroutestoprimitivecellsanexperimentalmodelbasedonthespontaneousentrapmentofenzymesinsidemicrometersizedliposomes |