scholarly journals Crystal Structure of the MACPF Domain of Human Complement Protein C8α in Complex with the C8γ Subunit

2008 ◽  
Vol 379 (2) ◽  
pp. 331-342 ◽  
Author(s):  
Daniel J. Slade ◽  
Leslie L. Lovelace ◽  
Maksymilian Chruszcz ◽  
Wladek Minor ◽  
Lukasz Lebioda ◽  
...  
Biochemistry ◽  
2002 ◽  
Vol 41 (22) ◽  
pp. 7030-7037 ◽  
Author(s):  
Eric Ortlund ◽  
Chasta L. Parker ◽  
Steven F. Schreck ◽  
Steve Ginell ◽  
Wladek Minor ◽  
...  

2007 ◽  
Vol 367 (1) ◽  
pp. 224-233 ◽  
Author(s):  
Vengadesan Krishnan ◽  
Yuanyuan Xu ◽  
Kevin Macon ◽  
John E. Volanakis ◽  
Sthanam V.L. Narayana

1973 ◽  
Vol 248 (8) ◽  
pp. 2818-2823
Author(s):  
Carlos R. Sledge ◽  
David H. Bing

1999 ◽  
Vol 341 (1) ◽  
pp. 61-69 ◽  
Author(s):  
Rajneesh MALHOTRA ◽  
Malcolm WARD ◽  
Robert B. SIM ◽  
Michael I. BIRD

The selectin family of adhesion molecules (E-, P- and L-selectins) is involved in leukocyte recruitment to sites of inflammation and tissue damage. Recently it has been shown that L-selectin is involved not only in leukocyte tethering and rolling, but also plays an important role in leukocyte activation. For example, glycosylation-dependent cell-adhesion molecule 1 (GlyCAM-1), a known ligand for L-selectin, has been shown to enhance β2-integrin function. GlyCAM-1 is a secreted protein and is present in mouse serum at a concentration of approx. 1.5 μg/ml. There is no obvious GlyCAM-1 homologue in man and, to date, L-selectin ligand(s) from human serum have not been characterized. Therefore we have used L-selectin affinity chromatography, followed by ion-exchange chromatography, to isolate specific ligand(s) for L-selectin. Using this procedure, we have isolated three major glycoproteins of apparent molecular masses 170 kDa, 70 kDa and 50 kDa. The 170 kDa protein band was digested with trypsin and peptides were analysed by delayed extraction matrix-assisted laser desorption ionization MS and protein database searching. The 170 kDa protein was identified as the human complement protein Factor H. Human Factor H, isolated by a different method, was shown to bind specifically to L-selectin in the presence of CaCl2, and binding was inhibited by anti-L-selectin antibodies, fucoidan and lipopolysaccharide. Only a part of the purified Factor H preparation bound to immobilized L-selectin. The interaction of Factor H with leukocyte L-selectin was shown to induce the secretion of tumour necrosis factor-α (TNF-α). Pretreatment of Factor H with sialidase reduced both the binding of L-selectin to Factor H and the Factor H-induced L-selectin-mediated TNF-α secretion by leukocytes. Taken together, these results demonstrate that a post-translationally modified form of human plasma Factor H is a potential physiological ligand for L-selectin.


2003 ◽  
Vol 278 (47) ◽  
pp. 46974-46982 ◽  
Author(s):  
Christine Gaboriaud ◽  
Jordi Juanhuix ◽  
Arnaud Gruez ◽  
Monique Lacroix ◽  
Claudine Darnault ◽  
...  

2002 ◽  
Vol 267 (1) ◽  
pp. 7-16 ◽  
Author(s):  
Hiroshi Tsukamoto ◽  
Albert Tousson ◽  
Antonella Circolo ◽  
Richard B. Marchase ◽  
John E. Volanakis

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