Telomerase is a reverse transcriptase that is responsible for the addition of telomeric repeats on to the ends of eukaryotic chromosomes. The purple sea urchin, Strongylocentrotus purpuratus, telomerase enzyme is unique in that its telomerase RNA does not contain the ancestrally conserved CR4/5 domain and instead contains the functionally equivalent eCR4/5 domain. Binding between the purple sea urchin TRBD and eCR4/5 domain is currently poorly understood due to eCR4/5's unique structure. In this work the telomerase RNA binding domain, TRBD, of the purple sea urchin telomerase reverse transcriptase, TERT, was fused to maltose binding protein (MBP) using several different short amino acid linkers and purified via amylose column purification. Short amino acid linkers were cloned into the MBP sea urchin TRBD constructs to facilitate better crystallization of the fusion protein. Future work of this project includes testing telomerase RNA binding affinity to the TRBD constructs and determining the crystal structure of the sea urchin TRBD with bound eCR4/5. Elucidating how eCR4/5 binds to the sea urchin TRBD will provide insights into the evolutionary relationship between eCR4/5 and the pseudoknot/template domain of sea urchin telomerase RNA.