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Explores how spin-selective chemistry affects neural signaling in biological systems, suggesting future research directions.
This paper asks whether spin-selective chemistry in a named protein or receptor can make a causal difference to what a neural receiver does next. The paper begins from established facts: protein state changes neural signaling, and spin chemistry can change the branching of particular molecular reactions. It then separates three increasingly strong proposals. A brief spin event may leave a longer-lived classical protein state; that state may participate in a memory operation; or a spin degree of freedom may itself store selectively writable and readable task information. Evidence for the first proposal is not treated as evidence for the third. The main contribution is a molecule-to-report decision program. It requires an identified spin system, a measured reaction consequence, a classical protein or receptor transducer, a receiver-specific neural effect, and a task-specific perceptual, mnemonic, choice, action, or report effect. Matched spin-insensitive variants, temporal ordering, blockade, two kinds of rescue, held-out prediction, and independent replication are used to distinguish spin effects from ordinary chemistry and global impairment. Recent engineered protein systems make spin preparation, measurement, and control in living biological settings increasingly tractable. They do not yet establish an endogenous neural spin mechanism. The paper therefore presents a falsifiable route into Self Aware Networks, Neural Array Projection Oscillation Tomography, and Phase Wave Differentials rather than claiming that the route has already been observed. This is version 1.0 of the preprint.
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Micah Blumberg (2026) studied this question.
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