Despite extensive efforts spanning multiple decades, the development of highly effective Ca 2+ sensitizers for the heart remains an elusive goal. Existing Ca 2+ sensitizers have other targets in addition to cardiac troponin (cTn), which can lead to adverse side effects, such as hypotension or arrhythmias. Thus, there is a need to design Ca 2+ -sensitizing drugs with higher affinity and selectivity for cTn. Previously, we determined that many compounds based on diphenylamine (DPA) were able to bind to a cTnC-cTnI chimera with moderate affinity (K d 10-120 μM). Of these compounds, 3-chlorodiphenylamine (3-Cl-DPA) bound most tightly (K d of 10 μM). Here, we investigate 3-Cl-DPA further and find that it increases the Ca 2+ sensitivity of force development in skinned cardiac muscle. Using NMR, we show that, like the known Ca 2+ sensitizers, trifluoperazine (TFP) and bepridil, 3-Cl-DPA is able to bind to the isolated N-terminal domain (N-domain) of cTnC (K d of 6 μM). However, while the bulky molecules of TFP and bepridil stabilize the open state of the N-domain of cTnC, the small and flexible 3-Cl-DPA molecule is able to bind without stabilizing this open state. Thus, unlike TFP, which drastically slows the rate of Ca 2+ dissociation from the N-domain of isolated cTnC in a dose-dependent manner, 3-Cl-DPA has no effect on the rate of Ca 2+ dissociation. On the other hand, the affinity of 3-Cl-DPA for a cTnC-TnI chimera is at least an order of magnitude higher than that of TFP or bepridil, likely because 3-Cl-DPA is less disruptive of cTnI binding to cTnC. Therefore, 3-Cl-DPA has a bigger effect on the rate of Ca 2+ dissociation from the entire cTn complex than TFP and bepridil. Our data suggest that 3-Cl-DPA activates the cTn complex via a unique mechanism and could be a suitable scaffold for the development of novel treatments for systolic heart failure.
CITATION STYLE
Tikunova, S. B., Cuesta, A., Price, M., Li, M. X., Belevych, N., Biesiadecki, B. J., … Davis, J. P. (2019). 3-Chlorodiphenylamine activates cardiac troponin by a mechanism distinct from bepridil or TFP. Journal of General Physiology, 151(1), 9–17. https://doi.org/10.1085/jgp.201812131
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