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Functional crosstalk between cell-surface and intracellular channels mediated by junctophilins essential for neuronal functions. Cerebellum 7 , — Anderie, I. Cell Signal 19 , — Goldstein, B. Tyrosine dephosphorylation and deactivation of insulin receptor substrate-1 by protein-tyrosine phosphatase 1B.

Possible facilitation by the formation of a ternary complex with the Grb2 adaptor protein. Helle, S. Organization and function of membrane contact sites. Acta , — Leitman, J. Compartmentalization of endoplasmic reticulum quality control and ER-associated degradation factors.

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    Table of Contents

    Quintana, A. Sustained activity of calcium release-activated calcium channels requires translocation of mitochondria to the plasma membrane. Poburko, D.

    Table of Contents

    Cell Calcium 40 , — Giorgi, C. Structural and functional link between the mitochondrial network and the endoplasmic reticulum. Wieckowski, M. Isolation of mitochondria-associated membranes and mitochondria from animal tissues and cells. England, M.

    Lipid raft

    Influence of antioxidants mannitol and allopurinol on oxygen free radical generation during and after cardiopulmonary bypass. Circulation 74 , — Nur, T. Starvation and refeeding regulate glycogen synthase gene expression in rat liver at the posttranscriptional level. The fluid mosaic model explains changes in structure and behavior of cell membranes under different temperatures, as well as the association of membrane proteins with the membranes.

    Local Palmitoylation Cycles and Specialized Membrane Domain Organization - Search

    While Singer and Nicolson had substantial evidence drawn from multiple subfields to support their model, recent advances in fluorescence microscopy and structural biology have validated the fluid mosaic nature of cell membranes. Additionally, the two leaflets of biological membranes are asymmetric and divided into subdomains composed of specific proteins or lipids, allowing spatial segregation of biological processes associated with membranes.

    Cholesterol and cholesterol-interacting proteins can concentrate into lipid rafts and constrain cell signaling processes to only these rafts. The existence of non-bilayer lipid formations with important biological functions was confirmed subsequent to publication of the fluid mosaic model. These membrane structures may be useful when the cell needs to propagate a non bilayer form, which occurs during cell division and the formation of a gap junction.

    Featured channels

    The membrane bilayer is not always flat. Local curvature of the membrane can be caused by the asymmetry and non-bilayer organization of lipids as discussed above. More dramatic and functional curvature is achieved through BAR domains , which bind to phosphatidylinositol on the membrane surface, assisting in vesicle formation, organelle formation and cell division. During the decade of , it was acknowledged that individual lipid molecules undergo free lateral diffusion within each of the layers of the lipid membrane.

    Cell membrane

    However, flip-flop might be enhanced by flippase enzymes. The processes described above influence the disordered nature of lipid molecules and interacting proteins in the lipid membranes, with consequences to membrane fluidity, signaling, trafficking and function.

    There are restrictions to the lateral mobility of the lipid and protein components in the fluid membrane imposed by the formation of subdomains within the lipid bilayer. These subdomains arise by several processes e.

    Lipid rafts are membrane nanometric platforms with a particular lipid and protein composition that laterally diffuse, navigating on the liquid bilipid layer. Sphingolipids and cholesterol are important building blocks of the lipid rafts. Cell membrane proteins and glycoproteins do not exist as single elements of the lipid membrane, as first proposed by Singer and Nicolson in Rather, they occur as diffusing complexes within the membrane.

    Some proteins embedded in the bilipid layer interact with the extracellular matrix outside the cell, cytoskeleton filaments inside the cell, and septin ring-like structures. These interactions have a strong influence on shape and structure, as well as on compartmentalization. Moreover, they impose physical constraints that restrict the free lateral diffusion of proteins and at least some lipids within the bilipid layer. When integral proteins of the lipid bilayer are tethered to the extracellular matrix, they are unable to diffuse freely.

    Proteins with a long intracellular domain may collide with a fence formed by cytoskeleton filaments. Furthermore, identification and characterization of DHHC Asp-His-His-Cys palmitoylating enzyme-substrate pairs have contributed to elucidating the regulatory mechanisms and pathophysiological significance of protein palmitoylation. Here, we review the recent progress in protein palmitoylation at the molecular, cellular, and in vivo level and discuss how locally regulated palmitoylation machinery works for dynamic nanoscale organization of membrane domains.

    AB - Palmitoylation is an evolutionally conserved lipid modification of proteins.