Pig sperm membrane microdomains contain a highly glycosylated 15–25-kDa wheat germ agglutinin-binding protein

2012 ◽  
Vol 426 (3) ◽  
pp. 356-362 ◽  
Author(s):  
Waraporn Kasekarn ◽  
Takeru Kanazawa ◽  
Kazuki Hori ◽  
Tomoyuki Tsuchiyama ◽  
Xue Lian ◽  
...  
1995 ◽  
Vol 144 (2) ◽  
pp. 153-165 ◽  
Author(s):  
Padmaja Mehta ◽  
Surekha Zingde ◽  
Suresh Advani ◽  
Hema Desai ◽  
Balwant Gothoskar

1990 ◽  
Vol 68 (4) ◽  
pp. 699-704 ◽  
Author(s):  
Yuzuru Kubohara ◽  
Koji Okamoto

A new stalk-specific wheat germ agglutinin (WGA) binding protein, wst34, has been identified in Dictyostelium discoideum and purified by the use of preparative sodium dodecyl sulfate - polyacrylamide gel electrophoresis and a WGA-affinity column. In normal development, wst34 appears during culmination and is maintained in stalk cells. It has a molecular mass of 34 kilodaltons and a pI value of 5.5–6.5. A polyclonal antiserum raised against stalk cell proteins of Dictyostelium mucoroides recognizes wst34 in western blots of D. discoideum proteins.Key words: Dictyostelium discoideum, Dictyostelium mucoroides, wheat germ agglutinin.


1988 ◽  
Vol 6 (5) ◽  
pp. 347-362 ◽  
Author(s):  
Giuliano Elia ◽  
Maria Ferrantini ◽  
Filippo Belardelli ◽  
Enrico Proietti ◽  
Ion Gresser ◽  
...  

1989 ◽  
Vol 62 (02) ◽  
pp. 815 ◽  
Author(s):  
Marjorie B Zucker ◽  
Robert A Grant ◽  
Evelyn A Mauss

2006 ◽  
Vol 6 (9) ◽  
pp. 2959-2966 ◽  
Author(s):  
Na Zhang ◽  
Qineng Ping ◽  
Guihua Huang ◽  
Xiuzhen Han ◽  
Yanna Cheng ◽  
...  

Wheat germ agglutinin (WGA) modified liposomes and solid lipid nanoparticles (SLNs) were evaluated for improving intestinal absorption of insulin. In an in situ local intestinal perfusion experiment, formulations containing 100 IU/kg insulin were administered to the duodenum, jejunum, and ileum of fasted rats. As hypothesized, ileum was the best intestinal location for the absorption of insulin-containing liposomes. Serum insulin concentrations decreased for the various formulations in different absorption sites according to the following trends: Duodenum > ileum > jejunum for WGA-modified insulin-containing liposomes; duodenum > jejunum > ileum for WGA-modified insulin-containing SLNs; ileum > jejunum > duodenum for insulin-containing liposomes; ileum > duodenum > jejunum for insulin-containing SLNs; and duodenum ≥ ileum > jejunum for aqueous solution of insulin. These results imply that the nanoparticle type and delivery site were important factors with respect to increasing the bioavailability of insulin following oral administration. The proteolytic degradation as well as the epithelial permeability were primary determinants influcing insulin mucosal absorption.


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