Development and characterization of a formulation based covalent conjugation with polyacrylic acid and recombinant major surface antigen (SAG1) of Toxoplasma gondii

被引:1
作者
Koc, Rabia Cakir [1 ]
Kilinc, Yasemin Budama [1 ]
机构
[1] Yildiz Tech Univ, Dept Bioengn, TR-34210 Istanbul, Turkey
来源
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI | 2017年 / 42卷 / 06期
关键词
Polymer; Protein; Conjugation; Toxoplasma gondii; Fluorescence; LIGHT-SCATTERING; PROTEIN; VACCINE; CHROMATOGRAPHY; IMMUNIZATION; MICE;
D O I
10.1515/tjb-2016-0158
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Toxoplasmosis is a major disease caused by Toxoplasma gondii that infects approximately half the world's population. The development of an effective vaccine would be extremely valuable for preventing disease. SAG1 is a major surface antigen of parasites and one of the most antigenic proteins of T. gondii. Developing highly antigenic and effective vaccine formulations using new generations of adjuvants and delivery systems is very important. Polyacrylic acid (PAA) is a polymer that increases the immunogenicity of an antigen to which it is covalently linked. The aim of this study was to develop a new formulation candidate with high stability and immunogenicity potential against toxoplasmosis via a covalent conjugation of PAA and the SAG1 protein. Methods: 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 of T. gondii was conjugated to a PAA polymer, SEC and fluorescence spectra results. Discussion and conclusion: The obtained SAG1-PAA conjugate can be used for vaccine development against T. gondii in future.
引用
收藏
页码:643 / 646
页数:4
相关论文
共 16 条
[1]   Immunization with a DNA plasmid encoding the SAG1 (P30) protein of Toxoplasma gondii is immunogenic and protective in rodents [J].
Angus, CW ;
Klivington-Evans, D ;
Dubey, JP ;
Kovacs, JA .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (01) :317-324
[2]   Development of a vaccine for toxoplasmosis: current status [J].
Bhopale, GM .
MICROBES AND INFECTION, 2003, 5 (05) :457-462
[3]  
Bruna-Romero O, 2012, CURRENT TOPICS IN TROPICAL MEDICINE, P169
[4]   DNA immunization with eukaryotic initiation factor-2α of Toxoplasma gondii induces protective immunity against acute and chronic toxoplasmosis in mice [J].
Chen, Jia ;
Huang, Si-Yang ;
Zhou, Dong-Hui ;
Li, Zhong-Yuan ;
Petersen, Eskild ;
Song, Hui-Qun ;
Zhu, Xing-Quan .
VACCINE, 2013, 31 (52) :6225-6231
[5]   Induction of long-lasting protective immunity against Toxoplasma gondii in BALB/c mice by recombinant surface antigen 1 protein encapsulated in poly (lactide-co-glycolide) microparticles [J].
Chuang, Shu-Chun ;
Ko, Jing-Chun ;
Chen, Chaio-Ping ;
Du, Jia-Tze ;
Yang, Chung-Da .
PARASITES & VECTORS, 2013, 6
[6]  
Eroglu BI, 2011, TURK J BIOCHEM, V36, P222
[7]   Alkyl-esters of polyacrylic acid as vaccine adjuvants [J].
Hilgers, LAT ;
Nicolas, I ;
Lejeune, G ;
Dewil, E ;
Strebelle, M ;
Boon, B .
VACCINE, 1998, 16 (16) :1575-1581
[8]   Online size-exclusion high-performance liquid chromatography light scattering and differential refractometry methods to determine degree of polymer conjugation to proteins and protein-protein or protein-ligand association states [J].
Kendrick, BS ;
Kerwin, BA ;
Chang, BS ;
Philo, JS .
ANALYTICAL BIOCHEMISTRY, 2001, 299 (02) :136-146
[9]   Synthesis and characterization of antigenic influenza A M2e protein peptide-poly(acrylic) acid bioconjugate and determination of toxicity in vitro [J].
Kilinc, Yasemin Budama ;
Akdeste, Zeynep Mustafaeva ;
Koc, Rabia Cakir ;
Bagirova, Melahat ;
Allahverdiyev, Adil .
BIOENGINEERED, 2014, 5 (06) :357-362
[10]  
Mitra G, 1993, Hindustan Antibiot Bull, V35, P133