We and others have demonstrated that CD133+/CD44+ cells from established prostate cancer cell lines are also self-renewing and multipotent

July 28, 2017

acids of the A2 domain, showed that mutations in the sequence between residues 1653 and 1663 reduced the rate of cutting, whereas the wild-type 78 amino acid sequence was readily cleaved. This suggests that the mutation A1661G might destabilize the A2 LY2109761 biological activity domain fold as predicted in silico, but at the same time it might abolish recognition by the enzyme, such that cleavage is not observed. The results from the present study suggest a mechanistic model for the interaction between the A2 domain and the enzyme ADATMS13. Studies based on binding assays and mutagenesis have determined that docking of ADATMS13 domains onto specific segments of A2 is essential for the proteolytic function. Thus, unfolding of the A2 domain is necessary not only to expose the cryptic site but also for proper recognition by ADAMTS13. The first major event during unfolding is undocking of helix a6 which is shown here to be facilitated by disruptive mutations located in its vicinity. Besides exposing part of the hydrophobic core and facilitating further unfolding, undocking of a6 allows binding of the ADAMTS13 spacer domain. In fact, specific residues in the spacer domain have been recognized to interact with a C-terminal segment of A2 that includes a6 and this interaction has been determined to be essential for the isolated A2 PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22212565 domain to be efficiently cleaved. Unfolding then proceeds through several intermediates as further a helices and b strands are pulled one after the other from the native fold. The presence of intermediate states is likely to reduce floppiness of the unfolding A2 domain backbone allowing further domains of ADATMS13 to dock at a relatively lower entropic cost. For example, the disintegrin-like domain of ADAMTS13 has been shown to interact with Asp1614 in the a4-less loop of A2 thus correctly orienting the scissile bond towards the metalloprotease domain. It needs to be mentioned that additional binding sites are available to ADAMTS13 in full length VWF because Structural Basis of Type 2A VWD terminus and thus it is not likely to influence the destabilization mechanism of the C-terminal helix observed here. Furthermore, the simulations results are in agreement with the cleavage experiments despite these were performed in the presence of 2 mM of calcium. Thus it can be speculated that calcium might not significantly affect the unfolding pathway of the A2 domain, but as pointed out by a recent study it might reduce the amount of time when the scissile bond is available to ADATMS13 for cleavage. Understanding how different mutations affect the stability of the A2 domain might be relevant also to protein engineering. For example, the A2 domain could be used as a scaffold in biotechnological applications where force sensitivity is required. In this context, it would be interesting to also engineer mutants that make the A2 domain more resistant to cleavage by increasing the stability of the C-terminal helix. For example, mutating P1662 in a6 to an alanine or leucine should increase a helical propensity and improve packing of the hydrophobic core. A previous study showed that stabilizing the C-terminal helices of designed ankyrin repeat proteins dramatically increased the thermodynamic stability of the native state and eliminated an intermediate state in equilibrium refolding experiments. These two studies together indicate that local stabilization or destabilization of a protein through mutations can lead to an increase or decrease, respectively in ther