Cytoskeletal connectors: Deciphering the fundamental mechanisms of cytoskeletal dynamics and transport
National Institute of General Medical Sciences
PROJECT SUMMARY
The cytoskeleton is a dynamic network of filamentous structures, including microtubules and actin, that regulate
essential cellular processes such as cell shape, growth, and signaling. Cytoskeleton also serves as tracks for
molecular motors, which transport a variety of cellular cargoes, including organelles, macromolecules, and
vesicles. These cargoes are linked to motors by specialized connector proteins. Disruptions in connector proteins
are implicated in a range of neurodevelopmental and neurodegenerative diseases, as well as cancers. Despite
their importance, these proteins continue to be understudied, primarily due to their perceived role as passive
linkers and the technical challenges in working with them. However, recent discoveries suggest that connector
proteins may play more active roles, in some cases even have enzymatic functions. This proposal aims to
uncover mechanisms of connector protein functions through a detailed investigation of actin-microtubule and
motor-cargo interactions.
Actin and microtubules are linked by the spectraplakin family of large and evolutionarily conserved proteins,
critical for neuronal development and differentiation. Recent discoveries of ATPase domains within these
proteins suggest they may haves beyond simply linking cytoskeletal components. One goal of this
proposal is to investigate the role of spectraplakin’s ATPase domains via structural, biochemical, and cell biology
approaches. Another goal is to explore how dynamic changes in motor-cargo connectors facilitate the transport
of diverse cargoes along microtubule tracks. The focus will be on the cytoplasmic dynein-1 (dynein) and the
connectors (adaptors) that activate and link dynein to cargo. Dynein is a microtubule minus-end directed motor
that plays essential roles in cell division, and transports hundreds of different cellular cargoes. While several
motor-cargo connectors have been identified, the regulatory mechanisms enabling cargo transport are not fully
understood. We are investigating whether connector proteins work together to activate dynein movement and/or
facilitate cargo handoff between different dynein complexes. Using innovative approaches, including time-
resolved cryo-EM, complex in-vitro reconstitutions, and live-cell imaging in induced neurons, we are uncovering
critical mechanisms that govern cytoskeletal connector proteins, furthering our understanding of how the
cytoskeleton regulates essential cellular processes.