scholarly journals Watching Three-Dimensional Movements of Single Membrane Proteins in Lipid Bilayers

Biochemistry ◽  
2018 ◽  
Vol 57 (31) ◽  
pp. 4735-4740 ◽  
Author(s):  
Li Ma ◽  
Ying Li ◽  
Jianbing Ma ◽  
Shuxin Hu ◽  
Ming Li
Science ◽  
2013 ◽  
Vol 340 (6128) ◽  
pp. 48-52 ◽  
Author(s):  
Gabriel Villar ◽  
Alexander D. Graham ◽  
Hagan Bayley

Living cells communicate and cooperate to produce the emergent properties of tissues. Synthetic mimics of cells, such as liposomes, are typically incapable of cooperation and therefore cannot readily display sophisticated collective behavior. We printed tens of thousands of picoliter aqueous droplets that become joined by single lipid bilayers to form a cohesive material with cooperating compartments. Three-dimensional structures can be built with heterologous droplets in software-defined arrangements. The droplet networks can be functionalized with membrane proteins; for example, to allow rapid electrical communication along a specific path. The networks can also be programmed by osmolarity gradients to fold into otherwise unattainable designed structures. Printed droplet networks might be interfaced with tissues, used as tissue engineering substrates, or developed as mimics of living tissue.


1994 ◽  
Vol 258 ◽  
pp. 167-190 ◽  
Author(s):  
Stuart J. Bussell ◽  
Daniel A. Hammer ◽  
Donald L. Koch

Biological membranes can be considered two-dimensional fluids with suspended integral membrane proteins (IMPs). We have calculated the effect of hydrodynamic interactions on the various diffusion coefficients of IMPs in lipid bilayers. The IMPs are modelled as hard cylinders of radius a immersed in a thin sheet of viscosity μ and thickness h bounded by a fluid of low viscosity μ′. We have ensemble averaged the N-body Stokes equations to the pair level and have renormalized them following the methods of Batchelor (1972) and Hinch (1977). The lengthscale for the hydrodynamic interactions is λa = μh / μ′, Which is O (100a), and the slow decay of the interactions introduces new features in the renormalizations compared to the analogous analyses for three-dimensional suspensions of spheres.We have calculated the asymptotic limits for the short- and long-time tracer diffusivities, Ds and Dl, respectively, and for the gradient diffusivity, Dg, for ϕ [Lt ] 1 and λ [Gt ] 1, where ϕ is the IMP area fraction and λ = μh / (μ′a). The diffusivities are \begin{eqnarray*} D_s/D_0 &=& 1-2\phi[1-(1+\ln (2)-9/32)/(\ln(\lambda)-\gamma)], D_l/D_0 &=& D_s/D_0 - 0.07/(\ln(\lambda)-\gamma), D_g/D_0 &=& 1+\phi[-7+(6\ln(2)+7/16+0.37)/(\ln(\lambda)-\gamma)], \end{eqnarray*} where D0 is the diffusivity in the limit of zero area fraction, and γ = 0.577216 is Euler's constant. The results for Dl and Ds differ only slightly. The decrease in Dg/Do as ϕ increases contrasts with the result for spheres for which Dg/Do > 1.


2021 ◽  
Vol 21 ◽  
Author(s):  
Madhukar Garg ◽  
Anju Goyal ◽  
Sapna Kumari

: Cubosomes are highly stable nanostructured liquid crystalline dosage delivery form derived from amphiphilic lipids and polymer-based stabilizers converting it in a form of effective biocompatible carrier for the drug delivery. The delivery form comprised of bicontinuous lipid bilayers arranged in three dimensional honeycombs like structure provided with two internal aqueous channels for incorporation of number of biologically active ingredients. In contrast liposomes they provide large surface area for incorporation of different types of ingredients. Due to the distinct advantages of biocompatibility and thermodynamic stability, cubosomes have remained the first preference as method of choice in the sustained release, controlled release and targeted release dosage forms as new drug delivery system for the better release of the drugs. As lot of advancement in the new form of dosage form has bring the novel avenues in drug delivery mechanisms so it was matter of worth to compile the latest updates on the various aspects of mentioned therapeutic delivery system including its structure, routes of applications along with the potential applications to encapsulate variety drugs to serve health related benefits.


Membranes ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 562
Author(s):  
Miliça Ristovski ◽  
Danny Farhat ◽  
Shelly Ellaine M. Bancud ◽  
Jyh-Yeuan Lee

Lipid composition in cellular membranes plays an important role in maintaining the structural integrity of cells and in regulating cellular signaling that controls functions of both membrane-anchored and cytoplasmic proteins. ATP-dependent ABC and P4-ATPase lipid transporters, two integral membrane proteins, are known to contribute to lipid translocation across the lipid bilayers on the cellular membranes. In this review, we will highlight current knowledge about the role of cholesterol and phospholipids of cellular membranes in regulating cell signaling and how lipid transporters participate this process.


1988 ◽  
Vol 21 (4) ◽  
pp. 429-477 ◽  
Author(s):  
W. Kühlbrandt

As recently as 10 years ago, the prospect of solving the structure of any membrane protein by X-ray crystallography seemed remote. Since then, the threedimensional (3-D) structures of two membrane protein complexes, the bacterial photosynthetic reaction centres of Rhodopseudomonas viridis (Deisenhofer et al. 1984, 1985) and of Rhodobacter sphaeroides (Allen et al. 1986, 1987 a, 6; Chang et al. 1986) have been determined at high resolution. This astonishing progress would not have been possible without the pioneering work of Michel and Garavito who first succeeded in growing 3-D crystals of the membrane proteins bacteriorhodopsin (Michel & Oesterhelt, 1980) and matrix porin (Garavito & Rosenbusch, 1980). X-ray crystallography is still the only routine method for determining the 3-D structures of biological macromolecules at high resolution and well-ordered 3-D crystals of sufficient size are the essential prerequisite.


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