Structural Arrangement of Lens Fiber Cell Plasma Membrane Protein MP20

1998 ◽  
Vol 66 (4) ◽  
pp. 495-509 ◽  
Author(s):  
MARK L. ARNESON ◽  
CHARLES F. LOUIS
Keyword(s):  
Plasma Membrane ◽  
Membrane Protein ◽  
Fiber Cell ◽  
Lens Fiber ◽  
Plasma Membrane Protein ◽  
Cell Plasma Membrane ◽  
Lens Fiber Cell ◽  
Structural Arrangement ◽  
Cell Plasma

scholarly journals Structural Organization of the Lens Fiber Cell Plasma Membrane Protein MP18

1989 ◽  
Vol 264 (33) ◽  
pp. 19974-19978 ◽  
Author(s):  
A Galvan ◽  
P D Lampe ◽  
K C Hur ◽  
J B Howard ◽  
E D Eccleston ◽  
...  
Keyword(s):  
Plasma Membrane ◽  
Membrane Protein ◽  
Structural Organization ◽  
Fiber Cell ◽  
Lens Fiber ◽  
Plasma Membrane Protein ◽  
Cell Plasma Membrane ◽  
Lens Fiber Cell ◽  
Cell Plasma

scholarly journals Sendai-viral HN and F glycoproteins as probes of plasma-membrane protein catabolism in HTC cells. Studies with fusogenic reconstituted Sendai-viral envelopes

1987 ◽  
Vol 241 (3) ◽  
pp. 801-807 ◽  
Author(s):  
R T Earl ◽  
E E Billett ◽  
I M Hunneyball ◽  
R J Mayer
Keyword(s):  
Plasma Membrane ◽  
Membrane Protein ◽  
Plasma Membranes ◽  
Viral Proteins ◽  
Plasma Membrane Protein ◽  
Lysosomal Degradation ◽  
Cell Plasma ◽  
Degradation Rates ◽  
Htc Cells ◽  
Viral Envelopes

Reconstituted Sendai-viral envelopes (RSVE) were produced by the method of Vainstein, Hershkovitz, Israel & Loyter [(1984) Biochim. Biophys. Acta 773, 181-188]. RSVE are fusogenic unilamellar vesicles containing two transmembrane glycoproteins: the HN (haemagglutinin-neuraminidase) protein and the F (fusion) factor. The fate of the viral proteins after fusion-mediated transplantation of RSVE into hepatoma (HTC) cell plasma membranes was studied to probe plasma-membrane protein degradation. Both protein species are degraded at similar, relatively slow, rates (t1/2 = 67 h) in HTC cells fused with RSVE in suspension. Even slower degradation rates for HN and F proteins (t1/2 = 93 h) were measured when RSVE were fused with HTC cells in monolayer. Lysosomal degradation of the transplanted viral proteins is strongly implicated by the finding that degradation of HN and F proteins is sensitive to inhibition by 10 mM-NH4Cl (81%) and by 50 micrograms of leupeptin/ml (70%).

A review of traditional and emerging methods to characterize lipid–protein interactions in biological membranes

2015 ◽  
Vol 7 (17) ◽  
pp. 7076-7094 ◽  
Author(s):  
Chih-Yun Hsia ◽  
Mark J. Richards ◽  
Susan Daniel
Keyword(s):  
Plasma Membrane ◽  
Membrane Protein ◽  
Protein Interactions ◽  
Protein Structures ◽  
Biological Membranes ◽  
Biological Functions ◽  
Cell Plasma Membrane ◽  
Lipid Interactions ◽  
Cell Plasma ◽  
Lipid Protein Interactions

Lipid–protein interactions are essential for modulating membrane protein structures and biological functions in the cell plasma membrane. In this review we describe the salient features of classical and emerging methodologies for studying protein–lipid interactions and their limitations.

scholarly journals Lipid-Protein Interactions in Fiber Cell Plasma Membrane Isolated From Human and Porcine Eye Lenses

2017 ◽  
Vol 112 (3) ◽  
pp. 319a
Author(s):  
Marija Raguz ◽  
Laxman Mainali ◽  
William J. O‘Brien ◽  
Witold Karol Subczynski
Keyword(s):  
Plasma Membrane ◽  
Protein Interactions ◽  
Fiber Cell ◽  
Cell Plasma Membrane ◽  
Cell Plasma ◽  
Lipid Protein Interactions
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