Optical and Scanning Probe Analysis of Glycolipid Reorganization upon Concanavalin A Binding to Mannose-Coated Lipid Bilayers†

Langmuir ◽  
2003 ◽  
Vol 19 (5) ◽  
pp. 1829-1837 ◽  
Author(s):  
Bruce Bondurant ◽  
Julie A. Last ◽  
Tina A. Waggoner ◽  
Andrea Slade ◽  
Darryl Y. Sasaki
2012 ◽  
Vol 45 (3) ◽  
pp. 69-78
Author(s):  
S. H. Olsen ◽  
R. Kapoor ◽  
S. J. Bull

2021 ◽  
pp. 1-9
Author(s):  
Jonathan Op de Beeck ◽  
Jeroen E. Scheerder ◽  
Brian P. Geiser ◽  
Joseph H. Bunton ◽  
Robert M. Ulfig ◽  
...  

Reliable spatially resolved compositional analysis through atom probe tomography requires an accurate placement of the detected ions within the three-dimensional reconstruction. Unfortunately, for heterogeneous systems, traditional reconstruction protocols are prone to position some ions incorrectly. This stems from the use of simplified projection laws which treat the emitter apex as a spherical cap, although the actual shape may be far more complex. For instance, sampled materials with compositional heterogeneities are known to develop local variations in curvature across the emitter due to their material phase specific evaporation fields. This work provides three pivotal precursors to improve the spatial accuracy of the reconstructed volume in such cases. First, we show scanning probe microscopy enables the determination of the local curvature of heterogeneous emitters, thus providing the essential information for a more advanced reconstruction considering the actual shape. Second, we demonstrate the cyclability between scanning probe characterization and atom probe analysis. This is a key ingredient of more advanced reconstruction protocols whereby the characterization of the emitter topography is executed at multiple stages of the atom probe analysis. Third, we show advances in the development of an electrostatically driven reconstruction protocol which are expected to enable reconstruction based on experimental tip shapes.


1985 ◽  
Vol 63 (10) ◽  
pp. 1049-1057 ◽  
Author(s):  
Frances J. Sharom ◽  
Ian Lorimer ◽  
Mary P. Lamb

Pure 5′-nucleotidase (EC 3.1.3.5) and a membrane glycoprotein fraction (partially purified 5′-nucleotidase) were isolated from pig lymphocyte plasma membrane by affinity chromatography techniques, using the cationic detergent dodecyltrimethylammonium bromide as a solubilizing agent. A detergent-dialysis technique was used to reconstitute both partially purified and pure enzyme into large unilamellar phospholipid vesicles, where it remains functional. 5′-Nucleotidase is relatively unstable in detergent solutions, but is highly stable once reconstituted into lipid vesicles. Arrhenius plots of the enzyme in bilayers of dimyristoyl phosphatidylcholine show a break point at 22–23 °C, with a different activation energy above and below the phospholipid gel-to-liquid crystalline phase transition. 5′-Nucleotidase in intact plasma membrane is inhibited more than 95% by concanavalin A in a positively cooperative fashion (Hill coefficient = 2.1), as is partially purified reconstituted enzyme. Purification of the enzyme before reconstitution results in less than 50% inhibition by concanavalin A and a complete loss of positive cooperativity (Hill coefficient < 1.0). The inhibition properties of the enzyme can be fully restored by co-reconstituting pure 5′-nucleotidase with the remaining lymphocyte glycoproteins.


2021 ◽  
Vol 33 (11) ◽  
pp. 115002
Author(s):  
Gianlorenzo Bussetti ◽  
Rossella Yivlialin ◽  
Franco Ciccacci ◽  
Lamberto Duò ◽  
Eugenio Gibertini ◽  
...  

2002 ◽  
Vol 41 (Part 2, No. 2A) ◽  
pp. L149-L151 ◽  
Author(s):  
Hideki Minami ◽  
Kenji Itaka ◽  
Parhat Ahmet ◽  
Daisuke Komiyama ◽  
Toyohiro Chikyow ◽  
...  

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