Culminating Project Title
Protein Interaction Testing of TgCycY Putative Cyclin Protein of Toxoplasma gondii for a Novel Drug Target Identification
Date of Award
Culminating Project Type
Biological Sciences - Cell and Molecular: M.S.
College of Science and Engineering
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.
Keywords and Subject Headings
Toxoplasma gondii, TgCycY, TgDj-1, TgCDPK1, microneme secretion, protein-protein interaction
The apicomplexan protozoan parasites cause critical health problems and limitation of anti-parasitic drugs is a major problem. Among the apicomplexan parasites, Toxoplasma gondii (T. gondii) is a highly prevalent obligate intracellular protozoan parasite, which seems to rely mostly on proteins that are defined as cyclin and cell cycle kinases that needs to regulate the cell cycle of the tachyzoites. These proteins regulate DNA replication during the cell cycle and lead to moderate cell division which results toxoplasmosis disease. Before targeting the proteins in T. gondii, it is essential to identify these proteins and define their function in the cell cycle via protein-protein interactions. In vitro, protein-protein interaction testing of Toxoplasma gondii ME49 putative TgCycY cyclin via yeast two-hybrid screen was conducted to identify a protein interaction partner. Even though previously tested in vivo analyses showed no direct interaction between TgCycY and TgCrk2, TgCrk2 hypothesized as a potential interacting partner for the TgCycY with the association of a bridging protein. Hypotheses were made based on the ortholog TgCycY-TgCrk2 complex interactions in Homo sapiens, Drosophila melanogaster, and Saccharomyces cerevisiae. Among the identified 8 protein interaction partners from a cDNA library of asynchronous tachyzoite transcriptome that used in the Y2H screen, only TgDJ-1 protein was introduced as the potential interacting partner for the TgCycY. Other protein partners were excluded due to limitations of the yeast-two hybrid screen and lack of information. Based on the previous studies, TgDJ-1 protein has shown function involved in the micronemes secretion and it has introduced as the regulator of the Toxoplasma gondii secretion, motility, and invasion by interacting with TgCDPK1. TgDJ-1 inhibition did not affect the cell cycle of the tachyzoite. A CDK interacting partner for the TgCycY was not detected in this screen. Previously known fact of Cyclin Y function as a substrate for the CDK and the function of the mediating the ortholog CycY-CDK protein-protein interaction via a third protein was applied to the TgCycYTgDJ-1-TgCDPK1 predicted complex. Due to limitations of the current screen and obtained results, indicated hypotheses 1 & 2 cannot be proven and the results direct the conclusion towards the TgCycY having TgDJ-1 as a new protein interacting partner that has existing literature and role of outside the cell cycle regulation. Overall, our project aims to map at the molecular level interactions of putative TgCycY cyclin protein in vitro and identify its function in the T. gondii tachyzoites to introduce it as a novel drug target. Further study regarding the function of TgCycY-TgDJ-1-TgCDPK1 complex is needed to understand the TgCycY role in micronemes secretion and involvement in the tachyzoites.
Peiris, Wadumesthrige Dinusha Niranjali, "Protein Interaction Testing of TgCycY Putative Cyclin Protein of Toxoplasma gondii for a Novel Drug Target Identification" (2019). Culminating Projects in Biology. 39.
I would first like to thank my husband for continuous support, motivation, and encouragement throughout the program. Special thanks to my parents for guiding, supporting during the whole my educational career and letting me follow my dreams. Without their support, I would not be able to achieve the education that I dreamed. Second, I would also like to give my regards to my advisor Dr. Christopher Kvaal for the guidance, vision, and knowledge that he provided throughout the research project. He is a great scientist and a mentor that I met during my educational career and because of his support I could complete the program even I had to face the setbacks in my life. Special thanks to Dr. Timothy Schuh and Dr. Nathan Bruender not only for their comments, guidance and their knowledge for my thesis project but also for their support to write the thesis. Thanks to St Cloud State University, Graduate school, Department of Biology and Center for international studies for allowing me to complete the degree and experience a whole new level of research work that will build up steps for my future research career.