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Toropova, K.

Publications and source records attributed to Toropova, K..

3 recordsLinked to original sources

Context-bridged associative learning: linking neutral tone engram to fear through shared context

In associative fear learning, weak or temporally constrained training may fail to link a conditioned stimulus (CS) with an aversive unconditioned stimulus (US), particularly when the contextual representation is impaired (the immediate shock deficit). Here, we systematically tested behavioral conditions that enable linking of an initially neutral auditory memory trace to an aversive episode. Male C57BL/6 mice were studied in four experiments manipulating (i) preexposure to a CS tone, (ii) the duration of context exploration before immediate footshock, and (iii) whether CS memory was tested in a novel or a familiar-like context. A 5 s tone followed immediately by footshock did not induce reliable fear to either the CS or the training context. CS preexposure three days before conditioning did not facilitate CS aversive memory when animals were tested in a completely novel context. However, robust facilitation emerged when the CS memory was tested in a context similar to the preexposure/conditioning one, indicating strong contextual gating of CS retrieval. Extending context exploration before shock enabled CS fear learning, but reduced (and even reversed) the effect of CS preexposure, consistent with latent inhibition. Together, these results delineate behavioral constraints for linking an initially neutral cue memory to an aversive event and highlight contextual control over the coupling and expression of cue memory traces.

neuroscience↗

Beta-hairpin Mechanism of Autoinhibition and Activation in the Kinesin-2 Family

Members of the kinesin-2 family coordinate with other motors to power diverse physiological processes, but the structural mechanisms regulating kinesin-2 activity have been unknown. Distinctively, kinesin-2s canonically function as heterotrimers of two different motor subunits (e.g. Kif3A and Kif3B) and Kap3, but the role of heterotrimerization has yet to fully emerge. Here, we combine structural, cell biological, and single-molecule approaches to dissect kinesin-2 regulation as a heterodimer, heterotrimer, and quaternary complex with a cargo adaptor (APC). We identify a conserved motif in the tail of kinesin-2s (the beta-hairpin motif) that controls kinesin-2 motility by sequestering the motor domains away from their microtubule track, using striking molecular mimicry. Our data reveal how Kap3 binds via a multipartite interface with Kif3A and Kif3B, and - rather than activating motility directly - provides a platform on which cargo adaptors can engage and occlude the beta-hairpin motif. Together, these data articulate a structural framework for kinesin-2 activation, coordination with dynein, and adaptation for different biological functions.

cell biology↗

IFT-A Structure Reveals Carriages for Membrane Protein Transport into Cilia

Intraflagellar transport (IFT) trains are molecular machines that traffic proteins between cilia and the cell body. With a molecular weight over 80 MDa, each IFT train is a dynamic polymer of two large complexes (IFT-A and -B) and motor proteins, posing a formidable challenge to mechanistic understanding. Here, we reconstituted the complete human IFT-A complex and obtained its structure using cryo-EM. Combined with AlphaFold prediction and genome-editing studies, our results illuminate how IFT-A polymerizes; interacts with IFT-B; and uses an array of {beta}-propeller and TPR domains to create "carriages" of the IFT train that engage TULP adaptor proteins. We show that IFT-A{middle dot}TULP carriages are essential for cilia localization of diverse membrane proteins, as well as ICK - the key kinase regulating IFT train turnaround. These data establish a structural link between IFT-As distinct functions, provide a blueprint for the IFT-A train, and shed light on how IFT evolved from a proto-coatomer ancestor.

cell biology↗