ArticleACS chemical neuroscience2026
Transient Interactions of α-Synuclein N- and C-Termini.
Article in ACS chemical neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
α-Synuclein (αSyn) is a neuronal protein predominantly found at the synapse, involved in vesicle trafficking. αSyn aggregates are also the main component of Lewy bodies, the hallmarks of Parkinson's disease. Interactions between the N- and C-termini of αSyn play crucial roles in its behavior in solution, membrane binding, and aggregation. Studying these interactions provides valuable insights into the physiological and pathological functions of αSyn. Here, we employed photoinduced cross-linking of unmodified proteins (PICUP) to identify the transient contacts of αSyn in different conformational states. By using tyrosine-to-phenylalanine mutations to block the reactivity of specific amino acids, we establish key cross-links in each state. In solution, we identify internal contacts between the N- and C-termini of monomers, as well as intermonomer contacts between C-termini in oligomers. When αSyn is bound to membranes, the internal cross-linking is blocked, while the cross-linking between C-terminal regions persists. In fibrils, cross-linking is significantly reduced, primarily occurring between the C-termini of adjacent monomers. This work highlights the effectiveness of PICUP for reporting on the transient contacts involved in αSyn self-assembly and its coassembly with lipid membranes, while providing a streamlined protocol that opens avenues for studying protein-protein interactions for a wide range of systems.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.