scholarly journals Regulation Mechanisms for Molecular Diffusion in the Cell Membrane by the Membrane Skeleton: A Single Molecule Approach.

MEMBRANE ◽  
2002 ◽  
Vol 27 (2) ◽  
pp. 58-66
Author(s):  
Kotono Murase ◽  
Kenneth Ritchie ◽  
Takahiro Fujiwara ◽  
Ryota Iino ◽  
Chieko Nakada ◽  
...  
2002 ◽  
Vol 157 (6) ◽  
pp. 1071-1082 ◽  
Author(s):  
Takahiro Fujiwara ◽  
Ken Ritchie ◽  
Hideji Murakoshi ◽  
Ken Jacobson ◽  
Akihiro Kusumi

The diffusion rate of lipids in the cell membrane is reduced by a factor of 5–100 from that in artificial bilayers. This slowing mechanism has puzzled cell biologists for the last 25 yr. Here we address this issue by studying the movement of unsaturated phospholipids in rat kidney fibroblasts at the single molecule level at the temporal resolution of 25 μs. The cell membrane was found to be compartmentalized: phospholipids are confined within 230-nm-diameter (ϕ) compartments for 11 ms on average before hopping to adjacent compartments. These 230-nm compartments exist within greater 750-nm-ϕ compartments where these phospholipids are confined for 0.33 s on average. The diffusion rate within 230-nm compartments is 5.4 μm2/s, which is nearly as fast as that in large unilamellar vesicles, indicating that the diffusion in the cell membrane is reduced not because diffusion per se is slow, but because the cell membrane is compartmentalized with regard to lateral diffusion of phospholipids. Such compartmentalization depends on the actin-based membrane skeleton, but not on the extracellular matrix, extracellular domains of membrane proteins, or cholesterol-enriched rafts. We propose that various transmembrane proteins anchored to the actin-based membrane skeleton meshwork act as rows of pickets that temporarily confine phospholipids.


2001 ◽  
Vol 81 (1) ◽  
pp. 43-56 ◽  
Author(s):  
Guillaume Lenormand ◽  
Sylvie Hénon ◽  
Alain Richert ◽  
Jacqueline Siméon ◽  
François Gallet

Author(s):  
Qing Hao ◽  
Baruch B. Lieber

When a solute such as angiographic contrast is introduced into a solvent such as blood analog fluid flowing in a straight circular tube, it spreads under the combined action of molecule diffusion and the variation of velocity over the cross-section [8]. If two molecules are being carried in the flow, for example, one in the center and one near the wall, the rate of separation caused by the difference in bulk velocity will greatly exceed that caused by molecule motion. Given enough time, any single molecule would wander randomly throughout the cross section of the pipe because of molecular diffusion, and would sample at random all the advective velocities [4]. Therefore, Taylor [8] adopted the Lagrangian approach to the problem, casting the equations in a coordinate system that moves with the average velocity of the flow and replacing the molecular diffusion coefficient with a dispersion coefficient, and the local concentration with the cross sectional mean concentration. Recasting Taylor’s equation in an inertial coordinate system one obtained the so called advection-dispersion equation.


2002 ◽  
Vol 42 (supplement2) ◽  
pp. S223
Author(s):  
C. Nakada ◽  
Kenneth Ritchie ◽  
T. Fujiwara ◽  
M. Nakamura ◽  
Y. Oba ◽  
...  

FEBS Letters ◽  
2013 ◽  
Vol 587 (24) ◽  
pp. 3912-3920 ◽  
Author(s):  
Yong Yang ◽  
Joy Wolfram ◽  
Jianliang Shen ◽  
Yuliang Zhao ◽  
Xiaohong Fang ◽  
...  

2004 ◽  
Vol 86 (6) ◽  
pp. 4075-4093 ◽  
Author(s):  
Kotono Murase ◽  
Takahiro Fujiwara ◽  
Yasuhiro Umemura ◽  
Kenichi Suzuki ◽  
Ryota Iino ◽  
...  

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