Rapid Surface Shaving for Proteomic Identification of Novel Surface Antigens for Vaccine Development

2021 ◽  
pp. 47-62
Author(s):  
Laurence Don Wai Luu ◽  
Ruiting Lan
1988 ◽  
Vol 34 (4) ◽  
pp. 494-498 ◽  
Author(s):  
Michael R. W. Brown ◽  
Hosmin Anwar ◽  
J. William Costerton

2017 ◽  
Vol 42 (6) ◽  
Author(s):  
Rabia Cakir Koc ◽  
Yasemin Budama Kilinc

AbstractIntroduction:Toxoplasmosis is a major disease caused byMethods:PAA and SAG1 were covalently conjugated using a water-soluble carbodiimide crosslinker that activates carboxyl groups for spontaneous reaction with primary amines. To demonstrate conjugation of these molecules in size exclusion chromatography (SEC), fluorescence spectroscopy was used.Results:For the first time, one of the most important surface antigens ofDiscussion and conclusion:The obtained SAG1-PAA conjugate can be used for vaccine development against


Author(s):  
Amy K. Bei ◽  
Daniel B. Larremore ◽  
Kazutoyo Miura ◽  
Ababacar Diouf ◽  
Nicholas K. Baro ◽  
...  

As transmission intensity has declined in Senegal, so has the genetic complexity of circulating Plasmodium falciparum parasites, resulting in specific genotypes emerging and persisting over years. We address whether changes in parasite genetic signatures can alter the immune repertoire to variant surface antigens, and whether such responses can influence the expansion or contraction of specific parasite genotypes in the population. We characterize parasites within genotypic clusters, defined as identical by a 24-SNP molecular barcode and a haplotype identifier for other highly polymorphic loci; we measure expression of variant surface antigens (VSA) such as PfEMP-1 by transcript expression typing and expressed var DBL1α sequencing in ex vivo and short-term adapted RNA samples; and we measure IgG responses against VSAs from short-term adapted parasites. We find that parasites within genotypic clusters are genetically identical at other highly polymorphic loci. These parasites express similar Ups var classes and largely the same dominant var DBL1α sequences ex vivo. These parasites are recognized similarly by anti-VSA antibodies after short-term adaptation to culture; however, antibody responses do not correlate with genotype frequencies over time. Both genotype-specific and multiple genotype-reactive surface IgG responses are observed in this population. Parasites with identical genomes are extremely similar in their expression and host antibody recognition of VSAs. Monitoring changes in population-level parasite genomics and transmission dynamics is critical, as fluctuations will influence the breadth of resulting host immune responses to circulating parasite genotypes. These findings suggest shared immune recognition of genetically similar parasites, which has implications for both our understanding of immunity and vaccine development strategies in malaria elimination settings.


2015 ◽  
Vol 11 (2) ◽  
pp. 33-47
Author(s):  
Ashim K. Bagchi ◽  
Rushita A. Bagchi ◽  
Dipak K. Hens ◽  
Fahmida Jahan ◽  
Pragna H. Parikh ◽  
...  

1997 ◽  
Vol 6 (2) ◽  
pp. 81-95 ◽  
Author(s):  
Barbara Saxty ◽  
John Aitken

It has been estimated that 500 million couples world-wide have no access to contraception and that approximately 20% of births between 1995 and 2000 will be unwanted. Such statistics have important implications for the rate of world population growth and the possibility of maintaining a sustainable population. Although political change and the empowerment of women across the world will help address these issues, it will also be important to increase the availability of contraceptives; not only the modalities that are in current use, but also novel methods that will satisfy needs that are presently unfulfilled. One such alternative could be a vaccine targeting the human spermatozoon.


Author(s):  
K. Chien ◽  
I.P. Shintaku ◽  
A.F. Sassoon ◽  
R.L. Van de Velde ◽  
R. Heusser

Identification of cellular phenotype by cell surface antigens in conjunction with ultrastructural analysis of cellular morphology can be a useful tool in the study of biologic processes as well as in diagnostic histopathology. In this abstract, we describe a simple pre-embedding, protein A-gold staining method which is designed for cell suspensions combining the handling convenience of slide-mounted cell monolayers and the ability to evaluate specimen staining specificity prior to EM embedding.


Author(s):  
K. Chien ◽  
R. Van de Velde ◽  
I.P. Shintaku ◽  
A.F. Sassoon

Immunoelectron microscopy of neoplastic lymphoma cells is valuable for precise localization of surface antigens and identification of cell types. We have developed a new approach in which the immunohistochemical staining can be evaluated prior to embedding for EM and desired area subsequently selected for ultrathin sectioning.A freshly prepared lymphoma cell suspension is spun onto polylysine hydrobromide- coated glass slides by cytocentrifugation and immediately fixed without air drying in polylysine paraformaldehyde (PLP) fixative. After rinsing in PBS, slides are stained by a 3-step immunoperoxidase method. Cell monolayer is then fixed in buffered 3% glutaraldehyde prior to DAB reaction. After the DAB reaction step, wet monolayers can be examined under LM for presence of brown reaction product and selected monolayers then processed by routine methods for EM and embedded with the Chien Re-embedding Mold. After the polymerization, the epoxy blocks are easily separated from the glass slides by heatingon a 100°C hot plate for 20 seconds.


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