Physical limits of cells and proteomes

被引:208
作者
Dill, Ken A. [1 ,2 ,3 ]
Ghosh, Kingshuk [4 ]
Schmit, Jeremy D. [5 ]
机构
[1] SUNY Stony Brook, Laufer Ctr Phys & Quantitat Biol, New York, NY 11794 USA
[2] SUNY Stony Brook, Dept Phys, New York, NY 11794 USA
[3] SUNY Stony Brook, Dept Chem, New York, NY 11794 USA
[4] Univ Denver, Dept Phys & Astron, Denver, CO 80209 USA
[5] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
cell biophysics; protein dynamics; protein stability; diffusion and folding; proteome modeling; PROTEIN STABILITY; SALT BRIDGES; DENATURED STATE; CONTACT ORDER; CHAIN-LENGTH; IN-VIVO; TEMPERATURE; DISTRIBUTIONS; EXTINCTIONS; CONTRIBUTE;
D O I
10.1073/pnas.1114477108
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
What are the physical limits to cell behavior? Often, the physical limitations can be dominated by the proteome, the cell's complement of proteins. We combine known protein sizes, stabilities, and rates of folding and diffusion, with the known protein-length distributions P(N) of proteomes (Escherichia coli, yeast, and worm), to formulate distributions and scaling relationships in order to address questions of cell physics. Why do mesophilic cells die around 50 degrees C? How can the maximal growth-rate temperature (around 37 degrees C) occur so close to the cell-death temperature? The model shows that the cell's death temperature coincides with a denaturation catastrophe of its proteome. The reason cells can function so well just a few degrees below their death temperature is because proteome denaturation is so cooperative. Why are cells so dense-packed with protein molecules (about 20% by volume)? Cells are packed at a density that maximizes biochemical reaction rates. At lower densities, proteins collide too rarely. At higher densities, proteins diffuse too slowly through the crowded cell. What limits cell sizes and growth rates? Cell growth is limited by rates of protein synthesis, by the folding rates of its slowest proteins, and-for large cells-by the rates of its protein diffusion. Useful insights into cell physics may be obtainable from scaling laws that encapsulate information from protein knowledge bases.
引用
收藏
页码:17876 / 17882
页数:7
相关论文
共 73 条
[1]  
Alberts B., 2002, The shape and structure of proteins, Vfourth, DOI 10.1093/aob/mcg023
[2]   Kinetic effects of temperature on rates of genetic divergence and speciation [J].
Allen, Andrew P. ;
Gillooly, James F. ;
Savage, Van M. ;
Brown, James H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (24) :9130-9135
[3]   Crowding and hydrodynamic interactions likely dominate in vivo macromolecular motion [J].
Ando, Tadashi ;
Skolnick, Jeffrey .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (43) :18457-18462
[4]  
[Anonymous], 2007, BIOL CANC
[5]   Adapting proteostasis for disease intervention [J].
Balch, William E. ;
Morimoto, Richard I. ;
Dillin, Andrew ;
Kelly, Jeffery W. .
SCIENCE, 2008, 319 (5865) :916-919
[6]   Entropic stabilization of proteins and its proteomic consequences [J].
Berezovsky, IN ;
Chen, WW ;
Choi, PJ ;
Shakhnovich, EI .
PLOS COMPUTATIONAL BIOLOGY, 2005, 1 (04) :322-332
[7]   Cytoplasmic diffusion: molecular motors mix it up [J].
Brangwynne, Clifford P. ;
Koenderink, Gijsje H. ;
MacKintosh, Frederick C. ;
Weitz, David A. .
JOURNAL OF CELL BIOLOGY, 2008, 183 (04) :583-587
[8]   Thermal Adaptation of Viruses and Bacteria [J].
Chen, Peiqiu ;
Shakhnovich, Eugene I. .
BIOPHYSICAL JOURNAL, 2010, 98 (07) :1109-1118
[9]   Thermodynamics and kinetics of non-native interactions in protein folding: A single point mutant significantly stabilizes the N-terminal domain of L9 by modulating non-native interactions in the denatured state [J].
Cho, JH ;
Sato, S ;
Raleigh, DP .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 338 (04) :827-837
[10]   The effects of disulfide bonds on the denatured state of barnase [J].
Clarke, J ;
Hounslow, AM ;
Bond, CJ ;
Fersht, AR ;
Daggett, V .
PROTEIN SCIENCE, 2000, 9 (12) :2394-2404