A Highly Selective Assay for Neutral Endopeptidase Based on the Cleavage of a Fluorogenic Substrate Related to Leu-Enkephalin

1996 ◽  
Vol 237 (2) ◽  
pp. 167-173 ◽  
Author(s):  
Krishnamurti M. Carvalho ◽  
Guy Boileau ◽  
Antonio C.M. Camargo ◽  
Luiz Juliano
1994 ◽  
Vol 219 (1) ◽  
pp. 87-95 ◽  
Author(s):  
N. Goudreau ◽  
C. Guis ◽  
J.M. Soleilhac ◽  
B.P. Roques

1998 ◽  
Vol 5 (1) ◽  
pp. 148A-148A
Author(s):  
S GREENBERG ◽  
J HIRTH ◽  
C MAGILL ◽  
K CLARK

1979 ◽  
Author(s):  
T Harada ◽  
M Ohki ◽  
M Niwa ◽  
S Iwanaga

Limulus hemocyte lysate contains a proclotting enzyme, which is transformed to the active clotting enzyme in the presence of gram-negative bacterial endotoxins. The clotting enzyme coagulates a clottable protein, named coagulogen, contained also in the lysate. This gelation reaction of the lysate, named Limulus test, has been widely employed as a simple and very sensitive assay method for endotoxins. We developed a new fluorogenic substrate, Boc-Leu-Gly-Arg-4-methylcoumarin amide, for Limulus clotting enzyme and established an enzymatic assay method for endotoxins, using the substrate. Because the endotoxin mediates the activation of proclotting enzyme in the lysate, the measurement of amidase activity could be applicable for quantitation of the endotoxins. In fact, the amidase activity determined fluorometrically increased by increasing concentration of E. coli 0111: B4 endotoxin added to the lysate, and a linear relationship between the toxin concentration and the activity was observed in the range of 5X10-6to 5xl0-2 µg endotoxin. The method was a fifty times more sensitive than that of the Limulus test and was very reproducible. However, the method was not directly applicable for the assay of endotoxins in circulating blood, as the amidase activity was strongly inhibited by antithrombin III and α2-plasmin inhibitor. Thus, some pretreatment with heat or chloroform on plasma samples before the assay was required.


2019 ◽  
Author(s):  
Yunyang Zhang ◽  
Janice Mui ◽  
Thimali Arumaperuma ◽  
James P. Lingford ◽  
ETHAN GODDARD-BORGER ◽  
...  

<p>The sulfolipid sulfoquinovosyl diacylglycerol (SQDG) and its headgroup, the sulfosugar sulfoquinovose (SQ), are estimated to harbour up to half of all organosulfur in the biosphere. SQ is liberated from SQDG and related glycosides by the action of sulfoquinovosidases (SQases). We report a 10-step synthesis of SQDG that we apply to the preparation of saturated and unsaturated lipoforms. We also report an expeditious synthesis of SQ and (<sup>13</sup>C<sub>6</sub>)SQ, and X-ray crystal structures of sodium and potassium salts of SQ. Finally, we report the synthesis of a fluorogenic SQase substrate, methylumbelliferyl a-D-sulfoquinovoside, and examination of its cleavage kinetics by two recombinant SQases.</p>


Hypertension ◽  
1995 ◽  
Vol 25 (4) ◽  
pp. 637-642 ◽  
Author(s):  
Joseph G. Motwani ◽  
Chim C. Lang ◽  
Gordon Cramb ◽  
Allan D. Struthers

Hypertension ◽  
1995 ◽  
Vol 25 (6) ◽  
pp. 1178-1184 ◽  
Author(s):  
Zaid A. Abassi ◽  
Shaban Kotob ◽  
Eliahu Golomb ◽  
Federico Pieruzzi ◽  
Harry R. Keiser

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