Fine structure of the band 3 protein in human red cell membranes: Freeze-fracture studies

1978 ◽  
Vol 8 (3) ◽  
pp. 325-335 ◽  
Author(s):  
Ronald S. Weinstein ◽  
Jena K. Khodadad ◽  
Theodore L. Steck
Biochemistry ◽  
1997 ◽  
Vol 36 (31) ◽  
pp. 9596-9604 ◽  
Author(s):  
Scott J. Yi ◽  
Shih-Chun Liu ◽  
Laura H. Derick ◽  
Murray ◽  
Jane E. Barker ◽  
...  

1990 ◽  
Vol 75 (2) ◽  
pp. 262-267 ◽  
Author(s):  
Helen M. Ranney ◽  
Gwen H. Rosenberg ◽  
Martin Morrison ◽  
Thomas J. Mueller

Parasitology ◽  
1994 ◽  
Vol 108 (3) ◽  
pp. 257-267 ◽  
Author(s):  
I. Crandall ◽  
I. W. Sherman

SUMMARYMurine monoclonal antibodies (Mabs) were produced by vaccination of Balb/c mice with live Plasmodium falciparum infected red cells (iRBC). The iRBC Mabs recognized altered forms of the human erythrocyte membrane protein band 3; however, these Mabs did not recognize the band 3 molecule in uninfected or ring-infected red cells. The location of epitopes was determined by studying the binding of the iRBC Mabs after selective proteolysis of band 3 as well as by the reactivity of these Mabs to synthetic peptides that corresponded to putative exofacial regions of band 3. Treatment of uninfected red cell membranes with trypsin under low ionic strength conditions resulted in exposure of cryptic epitopes of band 3 which were recognized by the iRBC Mabs. Several of the anti-iRBC Mabs (two of which were described previously) inhibited the in vitro adherence of infected erythrocytes to C32 amelanotic melanoma cells. A mouse polyclonal serum against a synthetic peptide based on an amino acid sequence motif of band 3 reacted (by immunostaining) only with the surface of iRBC and blocked adhesion. Thus, it appears that cryptic residues of the band 3 protein become exposed upon parasitization, and their presence contributes to the increased adhesiveness of the P. falciparum-infected red cell.


Biochemistry ◽  
2002 ◽  
Vol 41 (27) ◽  
pp. 8630-8637 ◽  
Author(s):  
Afolorunso Andrew Demehin ◽  
Omoefe O. Abugo ◽  
Rajadas Jayakumar ◽  
Joseph R. Lakowicz ◽  
Joseph M. Rifkind

Blood ◽  
1967 ◽  
Vol 29 (5) ◽  
pp. 780-789 ◽  
Author(s):  
RONALD S. WEINSTEIN ◽  
STANLEY BULLIVANT

Abstract A simplified freeze-cleave and replication method of tissue preparation for examination in the electron microscope is applied to studies on red blood cell fine structure. With this technic, the cytoplasm of red blood cells appears to have a uniform pattern of packed granularity, with individual particles approximating the dimensions anticipated for replicas of individual hemoglobin molecules. The cell surface is smooth and partially covered with small particles which may represent antigens, enzymes, or some structural proteins. The possibility that particles seen in cells and on cell membranes may represent an artifact is discussed. Pretreatment of cells prior to freezing influences the plane of cleavage through packed cells so that the plane of cleavage can be preferentially directed either through the cytoplasm or along red cell membranes. The freeze-cleave technic may be of particular value in applications where extensive areas of membrane must be surveyed, such as searching for leukemogenic viruses budding through cell membranes.


1985 ◽  
Vol 85 (1) ◽  
pp. 37-48 ◽  
Author(s):  
Peter L. Dorogi ◽  
A. K. Solomon

Blood ◽  
1967 ◽  
Vol 30 (6) ◽  
pp. 785-791 ◽  
Author(s):  
RONALD S. WEINSTEIN ◽  
ROGER A. WILLIAMS

Abstract Electron microscopic studies on dried isolated red cell ghosts have been reported to show lesions associated with cell membranes in paroxysmal nocturnal hemoglobinuria (PNH). In this study, carbon-platinum replicas of membranes of freeze-cleaved, partially hydrated PNH red cells and isolated PNH cell ghosts failed to confirm the existence of these abnormalities. This suggests that the previously described lesions are the products of drying artifacts, although they may reflect hidden structural differences between PNH and normal red cell membranes.


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