Reverse target screening identifies putative L-AAA targets in astrocyte-selective toxicity

Park, J. S.; Lee, S. J.

doi:10.1101/2025.10.21.683823

Home/Archive/bioRxiv

bioRxiv · 10.1101/2025.10.21.683823

Reverse target screening identifies putative L-AAA targets in astrocyte-selective toxicity

Park, J. S.·Lee, S. J.

View original source ↗Export metadata ↓

Abstract

L--aminoadipic acid (L-AAA) is widely used to ablate astrocytes, yet the molecular basis of its cell-type selectivity remains unclear. We combined structure-based reverse screening with an enantiomeric control D--aminoadipic acid (D-AAA), network propagation on a signed, directed interactome, and cell-type-resolved transcriptomics to nominate mechanistic targets of L-AAA. Two independent AlphaFold-enabled screens converged on a small set of proteins; integrating apoptosis connectivity and astrocyte enrichment prioritized pyruvate carboxylase (PC). Docking placed L-AAA in the pyruvate/acetyl-CoA pocket of PC and supported stereoselective engagement over D-AAA. These results motivate a testable model in which L-AAA limits PC-driven anaplerosis in astrocytes, constraining oxaloacetate/aspartate supply and redox buffering to lower the threshold for apoptosis. The workflow generalizes to polar metabolites that evade standard chemoproteomics and reframes how L-AAA-based astrocyte ablation should be interpreted. SignificanceL--aminoadipic acid is a staple tool for selective astrocyte ablation, but its molecular effectors have remained elusive. By unifying AlphaFold-enabled reverse screening with network-level apoptosis inference and single-cell expression filters, we nominate pyruvate carboxylase as a plausible mediator of L-AAA toxicity. The resulting metabolism-centric mechanism--partial inhibition of glial anaplerosis that depletes aspartate and erodes NADPH-glutathione buffering--offers concrete, falsifiable predictions and clarifies how L-AAA should be interpreted in vivo and in vitro. Our pipeline is broadly applicable to small, highly polar metabolites that are challenging to profile by conventional target-deconvolution approaches.

Explore related subjects

biochemistry Preprint

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

Park, J. S., Lee, S. J.. 2025-10-22. Reverse target screening identifies putative L-AAA targets in astrocyte-selective toxicity. https://doi.org/10.1101/2025.10.21.683823

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

bioRxiv2026

Hierarchical cysteine oxidation controls reversible amyloid formation in an ankyrin repeat protein

The formation of amyloids, including functional amyloids, is observed for an increasing number of proteins but the molecular mechanisms that control this structural transition remain poorly understood. Here we report that the kinase inhibitor protein P18 (drP18) from Danio rerio (zebrafish), which contains two cysteine residues, undergoes a complex and hierarchical redox switch that strictly governs reversible amyloid formation. We identify cysteine 50 (C50) acting as a regulatory residue. Upon oxidation, C50 forms an intramolecular disulfide bond with the executioner cysteine 128 (C128), thereby blocking it. C50 can become S-glutathionylated, and upon oxidation, C128 then forms intermolecular disulfides that lead to rapid transition into amyloid fibrils. S-glutathionylation of C50 therefore enables amyloid formation of drP18 and the outcome is oxidant-dependent with diamide, hydrogen peroxide, peroxymonocarbonate and hypothiocyanous acid each leading to amyloid assembly with distinct kinetics and morphologies. These amyloids are fully reversible, where disulfide reduction is leading to disassembly. Whereas monomeric drP18 inhibits CDK4-mediated retinoblastoma phosphorylation, the amyloid conformation abolishes this inhibition, and reduction restores both structure and function. Expression of drP18 in zebrafish embryos yields Congo red-positive, oxidation-dependent aggregates in vivo. Together, our findings show that a regulatory cysteine controls an executioner cysteine to induce reversible, functional amyloid formation, revealing that proteins can encode sophisticated mechanisms to control amyloid assembly.

biochemistry↗

bioRxiv2026

Snapshots from the Catalytic Landscape of Chalcone Isomerase

Chalcone isomerase (CHI) catalyzes the cyclization of 3-ring scaffolds of flavonoids, a class of plant-based natural products important for nutrition and disease prevention. A persistent question has been whether the enzyme uses dynamics to facilitate conformational rearrangements of substrates within the active site. To help resolve this question, CHI was crystallized with phloretin, a flexible substrate analogue that cannot undergo cyclization. The crystal structure possesses eight protein molecules per asymmetric unit, revealing different active site conformations that accommodate different bound conformers of phloretin. Together, the structural snapshots depict a series of coordinated, dynamic chemical interactions that lower barriers to substrate rearrangements approaching bond formation. Differential scanning fluorimetry combined with mutational analysis and enzyme kinetics further confirm that phloretin binds to the enzyme active site and that it acts as a competitive inhibitor of CHI. Together these findings answer outstanding questions about the flexibility and dynamics of CHI catalysis, information that may be useful for future biosynthetic design and enzyme engineering goals. Overall, this work supports a catalytic model in which the CHI enzyme operates as a dynamic ensemble of structures necessary to facilitate catalytic substrate rearrangements.

biochemistry↗

bioRxiv2026

Structures of pUG-fold RNA bound to DNMT1 reveal a mechanism for RNA-mediated epigenetic regulation

Many chromatin-associated proteins have been found to bind RNA as a means of epigenetic regulation. Specifically, DNA methyltransferase 1 (DNMT1), which maintains cytosine methylation at CpG dinucleotides, is inhibited by RNA at transcribed DNA loci in cells. However, the mechanisms by which RNA binds DNMT1 and inhibits its activity remain unknown. Here, we determine a series of cryogenic electron microscopy (cryo-EM) structures of human DNMT1 bound to pUG-fold RNA, a non-canonical G-quadruplex previously observed to inhibit activity, revealing two distinct RNA-binding modes. The pUG-fold RNA binds the surface of DNMT1 in its autoinhibited conformation across a positively charged surface between the methyltransferase domain and the CXXC domain, and it binds directly in the active site of an open DNMT1 conformation. RNA binding is sterically incompatible with substrate DNA engagement in both states. Our 2.5 [A] structure captures the intricate network of hydrogen bonds and electrostatic interactions between amino acids in the methyltransferase domain and the tetrad layers of pUG-fold RNA. Metadynamics molecular dynamics simulations provide an orthogonal view of the conformational landscape of DNMT1, revealing the two distinct RNA-binding modes. Furthermore, our analysis of published DNMT1 RIP-seq and eCLIP-seq data confirms that DNMT1-interacting RNAs in cells exhibit a strong propensity to form non-canonical G-quadruplex RNA structures. Collectively, our study provides the first structural basis for pUG-fold RNA recognition by a protein and illustrates how cryo-EM and AI-based methods for protein and RNA structure prediction synergize to inform the mechanism of RNA-mediated regulation of DNMT1.

biochemistry↗