2017
DOI: 10.1186/s13071-017-2387-y
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Screening and identification of host proteins interacting with Toxoplasma gondii SAG2 by yeast two-hybrid assay

Abstract: BackgroundThe identification of receptors or binding partners of Toxoplasma gondii from humans is an essential activity. Many proteins involved in T. gondii invasion have been characterized, and their contribution for parasite entry has been proposed. However, their molecular interactions remain unclear.ResultsYeast two-hybrid (Y2H) experiment was used to identify the binding partners of surface antigens of T. gondii by using SAG2 as bait. Colony PCR was performed and positive clones were sent for sequencing t… Show more

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Cited by 9 publications
(3 citation statements)
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References 30 publications
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“…The results obtained in the different research works reporting on the pathogenesis, immunogenicity, and treatment of T. gondii are worthy to be contextualized. The articles relative to Malaysia indicated some suitable proteins markers that can serve either for treatment or as good candidates for vaccine development [ 70 , 71 , 72 , 77 , 83 , 84 ]. Additionally, the fact that some of the drugs for the treatment of T. gondii are teratogenic and still no cure for the bradyzoite tissue cysts must be taken into consideration.…”
Section: Innovative Diagnostic Approach and Vaccine Development Fomentioning
confidence: 99%
“…The results obtained in the different research works reporting on the pathogenesis, immunogenicity, and treatment of T. gondii are worthy to be contextualized. The articles relative to Malaysia indicated some suitable proteins markers that can serve either for treatment or as good candidates for vaccine development [ 70 , 71 , 72 , 77 , 83 , 84 ]. Additionally, the fact that some of the drugs for the treatment of T. gondii are teratogenic and still no cure for the bradyzoite tissue cysts must be taken into consideration.…”
Section: Innovative Diagnostic Approach and Vaccine Development Fomentioning
confidence: 99%
“…The full length CtBSL (1006 bp), CtJAZ3 (1241 bp) and CtNINJA (1361 bp), CtMYC2 (1062 bp) gene sequences were cloned in pGBKT7 (bait) and pGADT7 (prey) plasmids, respectively, and subsequently transformed into yeast two hybrid GOLD strain (Clontech), using a Frozen-EZ Yeast Transformation II Kit (Zymo Research). The protein interactions were analyzed on SD medium containing X-α-Gal (40 ng/mL) and Aureobasidin A (125 ng/mL), using quadruple dropout method (Lai and Lau, 2017). The list of primers used in this study is given in Table S1.…”
Section: Yeast Two Hybrid Assaymentioning
confidence: 99%
“…The pGBKT7-evpP plasmid and empty pGBKT7 vector were transformed into the yeast strain Y2HGold using theYeast maker TM Yeast Transformation System 2 kit according to the manufacturer's manual (Clontech, Japan), respectively. Total proteins were detected using c-myc tag mouse McAb (Tianjin Saierbio, China) to detect evpP expression as described previously (Lai and Lau, 2017). The culture with recombinant pGBKT7-evpP bait were plated on SD/-Trp, SD/-Trp/X and SD/-Trp/X/A plates.…”
Section: Bait Plasmid Expression Auto-activation and Toxicity Testsmentioning
confidence: 99%