Sayaka Eno on Muck Rack

Sayaka Eno

As seen in: PLOS Biology, eLife
Is this you? As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work. Claim your profile

Get in touch with Sayaka

Contact Sayaka, search articles and posts on X, monitor coverage, and track replies from one place.

Learn more about Muck Rack

Actions

Share this page

Is this you?

As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.
Claim your profile

Articles

Profiling presynaptic scaffolds using split-GFP reconstitution reveals cell-type-specific spatial configurations in the fly brain

|
By Hongyang Wu, Yoh Maekawa, Sayaka Eno
| eLife
eLife Assessment This important work introduces a splitGFP-based labeling tool with an analysis pipeline for the synaptic scaffold protein bruchpilot, with tests in the adult Drosophila mushroom bodies, a learning center in the Drosophila brain. The evidence supporting the conclusions is convincing.
Open in Who Shared View Duplicates (3) Issue with article?

Octopamine signaling regulates the intracellular pattern of the presynaptic active zone scaffold within Drosophila mushroom body neurons

|
By Hongyang Wu, Sayaka Eno, Kyoko Jinnai, Ayako Abe
| PLOS Biology Verified
Loading metrics Open Access Peer-reviewed Research Article ? This is an uncorrected proof. Citation: Wu H, Eno S, Jinnai K, Abe A, Saito K, Maekawa Y, et al. (2025) Octopamine signaling regulates the intracellular pattern of the presynaptic active zone scaffold within Drosophila mushroom body neurons. PLoS Biol 23(10): e3003449.
Open in Who Shared Issue with article?

Octopamine signals coordinate the spatial pattern of presynaptic machineries within individual Drosophila mushroom body neurons

|
By Hongyang Wu, Sayaka Eno, Kyoko Jinnai, Yoh Maekawa
| biorxiv.org
Abstract Neurons need to adjust synaptic output according to the targets. However, the target-specific synaptic structures within individual neurons in the central nervous system remains largely unresolved, due to the high density of neuropils. Applying the CRISPR/Cas9-mediated split-GFP tagging, we devised cell-type specific fluorescent visualization of the endogenous active zone scaffold protein, Bruchpilot (Brp).
Open in Who Shared Issue with article?
See all 7 articles
 •  Privacy  •  Terms  •  Security and Legal  •   •   •   • 

© 2026 Muck Rack

SOC 2® Certified