Academic literature on the topic 'Supported lipid bilayer, ligand/receptor interactions'

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Journal articles on the topic "Supported lipid bilayer, ligand/receptor interactions"

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Biswas, Kabir H., and Jay T. Groves. "Hybrid Live Cell–Supported Membrane Interfaces for Signaling Studies." Annual Review of Biophysics 48, no. 1 (2019): 537–62. http://dx.doi.org/10.1146/annurev-biophys-070317-033330.

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A wide range of cell–microenvironmental interactions are mediated by membrane-localized receptors that bind ligands present on another cell or the extracellular matrix. This situation introduces a number of physical effects including spatial organization of receptor–ligand complexes and development of mechanical forces in cells. Unlike traditional experimental approaches, hybrid live cell–supported lipid bilayer (SLB) systems, wherein a live cell interacts with a synthetic substrate supported membrane, allow interrogation of these aspects of receptor signaling. The SLB system directly offers f
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Daniel, Susan, Fernando Albertorio, and Paul S. Cremer. "Making Lipid Membranes Rough, Tough, and Ready to Hit the Road." MRS Bulletin 31, no. 7 (2006): 536–40. http://dx.doi.org/10.1557/mrs2006.139.

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Solid-supported lipid bilayers hold strong promise as bioanalytical sensor platforms because they readily mimic the same multivalent ligand-receptor interactions that occur in real cells. Such devices might be used to monitor air and water quality under real-world conditions. At present, however, supported membranes are considered too fragile to survive the harsh environments typically required for non-laboratory use. Specifically, they lack the resiliency to withstand air exposure and the thermal and mechanical stresses associated with device transport, storage, and continuous use over long p
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Di Iorio, Daniele, Yao Lu, Joris Meulman, and Jurriaan Huskens. "Recruitment of receptors at supported lipid bilayers promoted by the multivalent binding of ligand-modified unilamellar vesicles." Chemical Science 11, no. 12 (2020): 3307–15. http://dx.doi.org/10.1039/d0sc00518e.

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The development of model systems that mimic biological interactions and allow the control of both receptor and ligand densities, is essential for a molecular understanding of biomolecular processes, such as the recruitment of receptors at interfaces.
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Alves, Anna Carolina Schneider, Reinaldo Antonio Dias, Luciano Porto Kagami, et al. "Beyond the "Lock and Key" Paradigm: Targeting Lipid Rafts to Induce the Selective Apoptosis of Cancer Cells." Current Medicinal Chemistry 25, no. 18 (2018): 2082–104. http://dx.doi.org/10.2174/0929867325666180111100601.

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For more than 40 years, the fluid mosaic model of cellular membranes has supported our vision of an inert lipid bilayer containing membrane protein receptors that are randomly hit by extracellular molecules to trigger intracellular signaling events. However, the notion that compartmentalized cholesterol- and sphingomyelin-rich membrane microdomains (known as lipid rafts) spatially arrange receptors and effectors to promote kinetically favorable interactions necessary for the signal transduction sounds much more realistic. Despite their assumed importance for the dynamics of ligand-receptor int
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Ghosh Moulick, R., D. Afanasenkau, S. E. Choi, et al. "Reconstitution of Fusion Proteins in Supported Lipid Bilayers for the Study of Cell Surface Receptor–Ligand Interactions in Cell–Cell Contact." Langmuir 32, no. 14 (2016): 3462–69. http://dx.doi.org/10.1021/acs.langmuir.5b04644.

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Jönsson, Peter, Jennifer H. Southcombe, Ana Mafalda Santos, et al. "Remarkably low affinity of CD4/peptide-major histocompatibility complex class II protein interactions." Proceedings of the National Academy of Sciences 113, no. 20 (2016): 5682–87. http://dx.doi.org/10.1073/pnas.1513918113.

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The αβ T-cell coreceptor CD4 enhances immune responses more than 1 million-fold in some assays, and yet the affinity of CD4 for its ligand, peptide-major histocompatibility class II (pMHC II) on antigen-presenting cells, is so weak that it was previously unquantifiable. Here, we report that a soluble form of CD4 failed to bind detectably to pMHC II in surface plasmon resonance-based assays, establishing a new upper limit for the solution affinity at 2.5 mM. However, when presented multivalently on magnetic beads, soluble CD4 bound pMHC II-expressing B cells, confirming that it is active and al
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Zhang, Yun, Yongzhi Qiu, Aaron T. Blanchard, et al. "Platelet integrins exhibit anisotropic mechanosensing and harness piconewton forces to mediate platelet aggregation." Proceedings of the National Academy of Sciences 115, no. 2 (2017): 325–30. http://dx.doi.org/10.1073/pnas.1710828115.

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Platelet aggregation at the site of vascular injury is essential in clotting. During this process, platelets are bridged by soluble fibrinogen that binds surface integrin receptors. One mystery in the mechanism of platelet aggregation pertains to how resting platelets ignore soluble fibrinogen, the third most abundant protein in the bloodstream, and yet avidly bind immobile fibrinogen on the surface of other platelets at the primary injury site. We speculate that platelet integrins are mechanosensors that test their ligands across the platelet–platelet synapse. To investigate this model, we in
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Wang, Li, Xin-Pu Hou, Angelica Ottova, and H. Ti Tien. "Receptor–ligand interactions in a reconstituted bilayer lipid membrane." Electrochemistry Communications 2, no. 5 (2000): 287–89. http://dx.doi.org/10.1016/s1388-2481(00)00008-4.

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Zhdanov, Vladimir P. "Ligand-receptor-mediated attachment of lipid vesicles to a supported lipid bilayer." European Biophysics Journal 49, no. 5 (2020): 395–400. http://dx.doi.org/10.1007/s00249-020-01441-0.

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Torres, Manuel, Catalina Ana Rosselló, Paula Fernández-García, Victoria Lladó, Or Kakhlon, and Pablo Vicente Escribá. "The Implications for Cells of the Lipid Switches Driven by Protein–Membrane Interactions and the Development of Membrane Lipid Therapy." International Journal of Molecular Sciences 21, no. 7 (2020): 2322. http://dx.doi.org/10.3390/ijms21072322.

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The cell membrane contains a variety of receptors that interact with signaling molecules. However, agonist–receptor interactions not always activate a signaling cascade. Amphitropic membrane proteins are required for signal propagation upon ligand-induced receptor activation. These proteins localize to the plasma membrane or internal compartments; however, they are only activated by ligand-receptor complexes when both come into physical contact in membranes. These interactions enable signal propagation. Thus, signals may not propagate into the cell if peripheral proteins do not co-localize wit
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Dissertations / Theses on the topic "Supported lipid bilayer, ligand/receptor interactions"

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Jung, Hyunsook. "SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES." 2009. http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-499.

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Ligand-receptor interactions are ubiquitous on cell membranes. Indeed, many important physiological functions primarily involve such interactions. These include cell signaling, pathogen binding, trafficking of lymphocytes, and the immune response.1-4 Therefore, studying ligand-receptor interactions at appropriate model membrane is of importance for both proper understanding of biological functions and applications to biosensors and bioseparations. Supported lipid bilayers are composed of the same lipid molecules found in the plasma cell membranes of living cells and possess the same two-dimens
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Book chapters on the topic "Supported lipid bilayer, ligand/receptor interactions"

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Saltzman, W. Mark. "Cell Adhesion." In Tissue Engineering. Oxford University Press, 2004. http://dx.doi.org/10.1093/oso/9780195141306.003.0011.

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The external surface of the cell consists of a phospholipid bilayer which carries a carbohydrate-rich coat called the glycocalyx; ionizable groups within the glycocalyx, such as sialic acid (N-acetyl neuraminate), contribute a net negative charge to the cell surface. Many of the carbohydrates that form the glycocalyx are bound to membrane-associated proteins. Each of these components— phospholipid bilayer, carbohydrate-rich coat, membrane-associated protein—has distinct physicochemical characteristics and is abundant. Plasma membranes contain ∼50% protein, ∼45% lipid, and ∼5% carbohydrate by weight. Therefore, each component influences cell interactions with the external environment in important ways. Cells can become attached to surfaces. The surface of interest may be geometrically complex (for example, the surface of another cell, a virus, a fiber, or an irregular object), but this chapter will focus on adhesion between a cell and a planar surface. The consequences of cell–cell adhesion are considered further in Chapter 8 (Cell Aggregation and Tissue Equivalents) and Chapter 9 (Tissue Barriers to Molecular and Cellular Transport). The consequences of cell–substrate adhesion are considered further in Chapter 7 (Cell Migration) and Chapter 12 (Cell Interactions with Polymers). Since the growth and function of many tissue-derived cells required attachment and spreading on a solid substrate, the events surrounding cell adhesion are fundamentally important. In addition, the strength of cell adhesion is an important determinant of the rate of cell migration, the kinetics of cell–cell aggregation, and the magnitude of tissue barriers to cell and molecule transport. Cell adhesion is therefore a major consideration in the development of methods and materials for cell delivery, tissue engineering, and tissue regeneration. The most stable and versatile mechanism for cell adhesion involves the specific association of cell surface glycoproteins, called receptors, and complementary molecules in the extracellular space, called ligands. Ligands may exist freely in the extracellular space, they may be associated with the extracellular matrix, or they may be attached to the surface of another cell. Cell–cell adhesion can occur by homophilic binding of identical receptors on different cells, by heterophilic binding of a receptor to a ligand expressed on the surface of a different cell, or by association of two receptors with an intermediate linker. Cell–matrix adhesion usually occurs by heterophilic binding of a receptor to a ligand attached to an insoluble element of the extracellular matrix.
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Conference papers on the topic "Supported lipid bilayer, ligand/receptor interactions"

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Murgasova, Renata, Jan Sabo, Angelica L. Ottova, and H. Ti Tien. "Ligand-receptor contact interactions using supported bilayer lipid membranes: cyclic voltammetry studies with electron mediators." In Smart Structures & Materials '95, edited by A. Peter Jardine. SPIE, 1995. http://dx.doi.org/10.1117/12.209816.

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