Development of an artificial cell, from self-organization to computation and self-reproduction

被引:218
作者
Noireaux, Vincent [2 ]
Maeda, Yusuke T. [1 ]
Libchaber, Albert [1 ]
机构
[1] Rockefeller Univ, New York, NY 10021 USA
[2] Univ Minnesota, Minneapolis, MN 55455 USA
基金
日本学术振兴会; 美国国家科学基金会;
关键词
FREE PROTEIN-SYNTHESIS; MYCOPLASMA-GENITALIUM GENOME; ESCHERICHIA-COLI GENOME; IN-VITRO; SYNTHETIC BIOLOGY; GENE-EXPRESSION; ALPHA-HEMOLYSIN; ENERGY CHARGE; LIPOSOMES; VESICLES;
D O I
10.1073/pnas.1017075108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This article describes the state and the development of an artificial cell project. We discuss the experimental constraints to synthesize the most elementary cell-sized compartment that can self-reproduce using synthetic genetic information. The original idea was to program a phospholipid vesicle with DNA. Based on this idea, it was shown that in vitro gene expression could be carried out inside cell-sized synthetic vesicles. It was also shown that a couple of genes could be expressed for a few days inside the vesicles once the exchanges of nutrients with the outside environment were adequately introduced. The development of a cell-free transcription/translation toolbox allows the expression of a large number of genes with multiple transcription factors. As a result, the development of a synthetic DNA program is becoming one of the main hurdles. We discuss the various possibilities to enrich and to replicate this program. Defining a program for self-reproduction remains a difficult question as nongenetic processes, such as molecular self-organization, play an essential and complementary role. The synthesis of a stable compartment with an active interface, one of the critical bottlenecks in the synthesis of artificial cell, depends on the properties of phospholipid membranes. The problem of a self-replicating artificial cell is a long-lasting goal that might imply evolution experiments.
引用
收藏
页码:3473 / 3480
页数:8
相关论文
共 101 条
  • [1] [Anonymous], 2004, Molecular Biology of the Cell
  • [2] ENERGY CHARGE OF ADENYLATE POOL AS A REGULATORY PARAMETER . INTERACTION WITH FEEDBACK MODIFIERS
    ATKINSON, DE
    [J]. BIOCHEMISTRY, 1968, 7 (11) : 4030 - &
  • [3] Imaging coexisting fluid domains in biomembrane models coupling curvature and line tension
    Baumgart, T
    Hess, ST
    Webb, WW
    [J]. NATURE, 2003, 425 (6960) : 821 - 824
  • [4] Life after the synthetic cell
    Bedau, Mark
    Church, George
    Rasmussen, Steen
    Caplan, Arthur
    Benner, Steven
    Fussenegger, Martin
    Collins, Jim
    Deamer, David
    [J]. NATURE, 2010, 465 (7297) : 422 - 424
  • [5] Cloning whole bacterial genomes in yeast
    Benders, Gwynedd A.
    Noskov, Vladimir N.
    Denisova, Evgeniya A.
    Lartigue, Carole
    Gibson, Daniel G.
    Assad-Garcia, Nacyra
    Chuang, Ray-Yuan
    Carrera, William
    Moodie, Monzia
    Algire, Mikkel A.
    Phan, Quang
    Alperovich, Nina
    Vashee, Sanjay
    Merryman, Chuck
    Venter, J. Craig
    Smith, Hamilton O.
    Glass, John I.
    Hutchison, Clyde A., III
    [J]. NUCLEIC ACIDS RESEARCH, 2010, 38 (08) : 2558 - 2569
  • [6] A relationship between membrane properties forms the basis of a selectivity mechanism for vesicle self-reproduction
    Bozic, B
    Svetina, S
    [J]. EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2004, 33 (07): : 565 - 571
  • [7] Exponential DNA replication by laminar convection
    Braun, D
    Goddard, NL
    Libchaber, A
    [J]. PHYSICAL REVIEW LETTERS, 2003, 91 (15)
  • [8] Protein length in eukaryotic and prokaryotic proteomes
    Brocchieri, L
    Karlin, S
    [J]. NUCLEIC ACIDS RESEARCH, 2005, 33 (10) : 3390 - 3400
  • [9] CAJAL SRY, 1908, PRIX NOBEL 1906
  • [10] Energizing cell-free protein synthesis with glucose metabolism
    Calhoun, KA
    Swartz, JR
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 2005, 90 (05) : 606 - 613