Cross-neutralization assays of Trimeresurus puniceus and Crotalus atrox venoms by Peruvian antivenoms

Toxicon ◽  
2020 ◽  
Vol 177 ◽  
pp. S35
Author(s):  
Jorge Alejandro Electo Oshiyama ◽  
Dan Erick Vivas-Ruiz ◽  
Alex Daniel Proleón Torres ◽  
Andres Agurto Arteaga ◽  
Fanny Lazo ◽  
...  
Author(s):  
Peter D. Moisiuk ◽  
Daniel R. Beniac ◽  
Ross A. Ridsdale ◽  
Martin Young ◽  
Bhushan Nagar ◽  
...  

Venom from the rattlesnake Crotalus atrox contains a mixture of enzymes that induce a localized effect leading to hemorrhaging, necrosis and edema. As a member of the crotalid family of snake venoms, Crotalus atrox venom contains a C-type lectin that will agglutinate blood cells in a Ca2+-dependent fashion. The lectin is a hydrophilic protein, consisting of two covalently linked, 135 amino acid residues, identical subunits that are rich in aspartic acid, glutamic acid and lysine. Sequence homology with known carbohydrate recognition domains (CRDs) indicates that rattlesnake venom lectin (RSLV) contains a CRD motif that is not linked to accessory domains. Preliminary X-ray diffraction and sedimentation analysis has indicated that lectin from Crotalus atrox forms decamers composed of two five-fold symmetric pentamers. Single particles of RSVL imaged at – 171°C displayed two distinct orientations on the specimen support (Figure a) following incubation in a crystallization Teflon well, coated with a lipid monolayer consisting of phosphatidylcholine and monosialoganglioside. When lying in an end-on orientation, the lectin exhibited a “pentagonal ring” with an outer diameter of 6.7 nm and an inner hollow core of 1.7 nm. A side orientation was also seen, whereby a thickness of 5.8 nm was measured for the lectin. Image processing of 2280 single particles placed in 100 classes (Figure b) led to 3D reconstructions of RSVL (Figure c). Density limited 3D reconstructions showed the lectin to be made of two five-fold symmetrical rings covalently linked between the five subunits that constitute each ring of this homodimer. These results are consistent with sedimentation and preliminary X-ray diffraction analysis on the shape of RSVL and provide the framework for structural verification by 2D electron crystallography.


1981 ◽  
Vol 256 (16) ◽  
pp. 8602-8607
Author(s):  
C. Keith ◽  
D.S. Feldman ◽  
S. Deganello ◽  
J. Glick ◽  
K.B. Ward ◽  
...  

Cell ◽  
2021 ◽  
Author(s):  
Johannes F. Scheid ◽  
Christopher O. Barnes ◽  
Basak Eraslan ◽  
Andrew Hudak ◽  
Jennifer R. Keeffe ◽  
...  
Keyword(s):  
B Cell ◽  

2002 ◽  
Vol 76 (13) ◽  
pp. 6480-6486 ◽  
Author(s):  
Alba-Lucia Combita ◽  
Antoine Touzé ◽  
Latifa Bousarghin ◽  
Neil D. Christensen ◽  
Pierre Coursaget

ABSTRACT The neutralizing activities of polyclonal antibodies and monoclonal antibodies (MAbs) obtained by immunization of mice with L1 virus-like particles (VLPs) were investigated by using pseudovirion infectivity assays for human papillomavirus type 16 (HPV-16), HPV-31, HPV-33, HPV-45, HPV-58, and HPV-59 to obtain a better definition of cross-neutralization between high-risk HPVs. In this study, we confirmed and extended previous studies indicating that most genital HPV genotypes represent separate serotypes, and the results suggest that the classification of serotypes is similar to that of genotypes. In addition, three cross-neutralizing MAbs were identified (HPV-16.J4, HPV-16.I23, and HPV-33.E12). MAb HPV-16.J4 recognized a conserved linear epitope located within the FG loop of the L1 protein, and HPV-16.I23 recognized another located within the DE loop. The results suggested that reactivity of MAb HPV-16.I23 to L1 protein is lost when leucine 152 of the HPV-16 L1 protein is replaced by phenylalanine. This confirmed the existence of linear epitopes within the L1 protein that induce neutralizing antibodies, and this is the first evidence that such linear epitopes induce cross-neutralization. However, the cross-neutralization induced by L1 VLPs represents less than 1% of the neutralizing activity induced by the dominant conformational epitopes, and it is questionable whether this is sufficient to offer cross-protection in vivo.


1970 ◽  
Vol 6 (1) ◽  
pp. 64
Author(s):  
Jeanine Saunders ◽  
Bob D. Johnson
Keyword(s):  

2012 ◽  
Vol 215 (15) ◽  
pp. 2630-2636 ◽  
Author(s):  
T. Kohl ◽  
S. E. Colayori ◽  
G. Westhoff ◽  
G. S. Bakken ◽  
B. A. Young

1965 ◽  
Vol 43 (3) ◽  
pp. 237-244 ◽  
Author(s):  
J Margolis ◽  
Sally Bruce ◽  
B Starzecki ◽  
GJ Horner ◽  
DFJ Halmagyi
Keyword(s):  

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