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Macromolecular crowding

T. C. Laurent, An early look at macromolecular crowding, Biophys. Chem. 57, 7 (1995). [Pg.145]

S. B. Zimmerman and A. P. Minton, Macromolecular crowding biochemical, biophysical, and physiological consequences, Annu. Rev. Biophys. Biomol. Struct. 22, 27 (1993). [Pg.145]

A. P. Minton, The influence of macromolecular crowding and macromolecular confinement on biochemical reactions in physiological media, J. Biol. Chem. 276, 10577 (2001). [Pg.145]

S. Schnell and T. E. Turner, Reaction kinetics in intracellular environments with macromolecular crowding simulations and rate laws, Prog. Biophys. Mol. Biol. 85, 235 (2004). [Pg.145]

D. Hall and A. P. Minton, Macromolecular crowding qualitative and semiquantitative successes, quantitative challenges, Biochim. Biophys. Acta (Proteins Proteomics) 1649, 127 (2003). [Pg.145]

Ellis RJ. Macromolecular crowding obvious but underappreciated. Trends Biochem. Sci. 2001 26 597-604. [Pg.279]

Leforestier, A. and Livolant, F. (1997) Liquid crystalline ordering of nucleosome core particles under macromolecular crowding conditions evidence for a discotic columnar hexagonal phase. Biophys. J. 73, 1771-1776. [Pg.418]

Johansson, H.-O., Brooks, D.E., Haynes, C.A. (2000). Macromolecular crowding and its consequences. International Review ofCy to logy, 192, 155-170. [Pg.111]

Minton, A.P., Colclasure, G.C., Parker, J.C. (1992). Model for the role of macromolecular crowding in regulation of cellular volume. Proc. Natl. Acad. Sci. USA 89,10504-10506. [Pg.208]

Garner, M.M., and M.B. Burg (1994). Macromolecular crowding and confinement in cells exposed to hypertonicity. Am. J. Physiol. 266 (Cell Physiol. 35) C877-C892. [Pg.286]

Most importantly, reaction rates in nanofluidic systems can be controlled both by shape and volume changes. The important interplay between chemical reactions and geometry has been conceptualized within a theoretical framework for ultra-small volumes and tested on a number of experimental systems, opening pathways to more complex, dynamically compartmentalized ultra-small volume reactors, or artificial model cells, that offer more detailed understanding of cellular kinetics and biophysical phenomena, such as macromolecular crowding. [Pg.466]

As weU as age-related reductions in cell volume, there may also be contributions to macromolecular crowding from age-related decline in proteasomal activity. Decreases in protein degradation would result in increases in the concentration of all cytoplasmic proteins. It has been found that inhibition of proteasomal activity leads to the formation of a-synuclein inclusions without, however, significantly increasing the concentration of a-synuclein. Reduced protease activity has been measured in Parkinson s disease brains. Also protease activity in PC12 cells is known to be reduced by over-expression of a-synuclein. [Pg.58]


See other pages where Macromolecular crowding is mentioned: [Pg.741]    [Pg.483]    [Pg.29]    [Pg.36]    [Pg.41]    [Pg.147]    [Pg.203]    [Pg.204]    [Pg.420]    [Pg.266]    [Pg.267]    [Pg.267]    [Pg.143]    [Pg.215]    [Pg.85]    [Pg.207]    [Pg.208]    [Pg.208]    [Pg.211]    [Pg.210]    [Pg.355]    [Pg.401]    [Pg.57]    [Pg.57]    [Pg.57]    [Pg.65]   
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