Abstract
The Protein Data Bank (PDB) contains approximately 188 thousand protein structures, 5000 of which have not been assigned a specific function. As a part of the Biochemistry Authentic Scientific Inquiry Laboratory (BASIL) project, we were tasked with analyzing and determining the function of one of these proteins, PDB ID 3r8e. This protein is a putative kinase, which is of interest due to the key roles kinases play in many cellular processes. Utilizing the modules the BASIL consortium provides, a series of in silico and in vitro experiments were conducted. The 3r8e protein was first studied using a variety of in silico tools, including BLASTp, Pfam, and DALI. Based on our in silico results, glucose was determined to be the most likely substrate for 3r8e and was used for further in vitro characterization of the protein. To confirm the in silico function prediction for the 3r8e protein, bacterial protein overexpression, affinity chromatography purification, and coupled kinase activity assays were utilized. Multiple sugar substrates for 3r8e were tested, including glucose. The coupled kinase assay results confirmed that 3r8e likely plays a role in glucose phosphorylation, aligning with our in silico conclusions. Future directions include repeating the above experiments and testing additional hexose substrates to further characterize the enzymatic activity of 3r8e. Overall, we have strong preliminary evidence that the 3r8e protein is a glucose kinase and future work will allow us to confirm this.
Introduction
Like many proteins with solved crystal structures, protein 3r8e has an uncharacterized and unconfirmed function. Besides the relationship with bacteria in soil, the role of this protein is still undetermined. Apart of a research project, our group set out to solve the function of this protein to then potentially provide further insight of the protein's relationship to the bacteria. Below is the general workflow of how we got our results.
Methods
As you can see in the workflow portion above, we used a variety of in silico tools such as BLASTp, Pfam, DALI, PyRx, and PyMol to help us generate a hypothesis for our uncharacterized proteins function. Using the FASTA sequence found in the Protein Data Bank file, we then were able to find similarities between 3r8e and other characterized proteins. While exploring the DALI database, a significant structural alignment hit was found with protein 3vov. Alignment and highly conserved amino acids can be seen below.
These results along with supporting evidence from the other in silico tools allowed us to then conduct in silico docking experiments to further confirm our hypothesis. Below is a figure with the PyRx docking results of glucose and ATP with our protein.
The -5.1 kcal/mol value shows that our protein of interest hypothesis of a glucose kinase is strong. The confidence behind our in silico results allowed us to move into testing our hypothesis in vitro. Because ATP is a commonality amongst sugar kinases, an has been provided to represent glucose and ATP in the active site.
Experimental Results/Function
Below are the results of our Uncoupled Kinase Assay. Our results from this assay further supports our idea of protein 3r8e assisting in the phosphorylation of glucose.
Project Implications
The goal of this project is to explore the methods it takes to characterize a putative kinase. To do this, we became familiar with online alignment, structure, and function tools, paired with a variety of in vitro lab experiments, such as bacterial protein overexpression, affinity chromatography, coupled kinase assays, and SDS PAGE Gel Electrophoresis. Proteins are biomolecules essential to organisms' survival and understanding how they work in result of their function is pivotal for advances in modern medicine, scientific research, and agriculture.
Conclusions/Future Direction
Conclusions:
- D-Glucose exhibited a specific activity of 4.22 ug/mL
- Specific activity: D-Glucose >> D-Galactose > D-Fructose > Lactose > D-Ribose
- Protein 3r8e is a Glucose Kinase
- Glucose is phosphorylated by our protein
Future Direction:
- Verify experimental results
- Publish results for further application
- Authenticate protein function using further kinase characterization protocols
