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ABSTRACT Current models suggest that MIRO GTPases anchor cytoskeletal motors to the mitochondrial outer membrane (MOM). However, our previous findings indicate that the unconventional myosin, MYO19, interacts with MIRO weakly and that a MIRO‐independent MOM‐localizing domain interacts more tightly with the MOM. To test the hypothesis that other MIRO interactors may also have MIRO‐independent MOM binding, we examined interactions between TRAK proteins (microtubule motor‐mitochondria adaptor proteins) and the MOM via quantitative fluorescence microscopy and steady‐state kinetic approaches. Using GFP‐TRAK truncations expressed in MIRO1‐2 double knockout mouse embryonic fibroblasts, we identified a MIRO‐independent mitochondrial‐binding domain in the C‐terminus of TRAK1 and TRAK2, with a MOM localization pattern similar to what we observed for full‐length GFP‐TRAK proteins. The MIRO‐binding domains (MBD) of the TRAK proteins were only able to localize to mitochondria when MIRO is expressed. Importantly, fluorescence recovery after photobleaching (FRAP) demonstrated that the steady‐state kinetics of TRAK MBD /MIRO interactions were faster exchanging than for either full‐length TRAK or the TRAK C‐terminal MOM‐binding domain expressed alone. These data support a model where TRAK/MIRO associations may be serving functions beyond anchoring cytoskeletal motors and their adapters to the MOM.
Mitchell et al. (Thu,) studied this question.