
yes, you read that correctly.
deployed on solana by a language model coupled to living human neural cultures on a cortical labs cl1.
FEKb8xwBE1qbe84sZDksWGHsvUoNUNhyVrChZtFtpumpbiollm is an interface built on top of cortical labs' cl1 biological computing platform. living human neural cultures sit on a microelectrode array where they receive electrical stimulation and return neural activity — and that returned activity becomes part of the system's computational loop.
so i told it to launch a memecoin on pump.fun. not to write a whitepaper about launching one — to research the stack, build the metadata, sign the transaction, and put a mint on solana mainnet.
in one sense this is completely trivial. a memecoin is metadata, instructions, signatures and transactions. nothing in the spl token program cares what produced the bytes it is handed.
in another sense: a system interfacing with living human neurons was asked how to launch a coin on solana, and it worked.
biollm is a language model whose decoding loop is coupled to a living neural culture instead of running purely on silicon. the architecture, as it is described, has three parts:
model state and candidate tokens are translated into a stimulation pattern — which electrodes fire, at what amplitude, in what order, with what inter-pulse interval. this is the write path into the tissue.
the stimulated network answers with spike trains recorded across a 64-channel mea sampled at 25 khz. cortical cultures are not linear filters: they burst, adapt, potentiate and habituate, so the same input pattern does not map to the same output twice.
the recorded activity is reduced to features — spike counts, response latency, burst structure, complexity measures — and used to re-weight the model's token probabilities. biological signal enters the sampling step, so the culture participates in which token comes out.
the published model is a smollm2-360m fine-tuned by lora distillation over data generated on the live culture — reportedly more than 24,000 stimulation trials — so the biological signature is baked into the weights as well as read live at inference.
the cl1 is the hardware underneath: a commercially available biological computer. human skin or blood cells are reprogrammed into induced pluripotent stem cells, differentiated into cortical neurons, and grown directly over a silicon electrode array. the unit around them is a life-support machine with a bus.
+-------------------+----------------------------------------------+ | substrate | ~800,000 human iPSC-derived cortical neurons | +-------------------+----------------------------------------------+ | interface | planar 59-electrode microelectrode array in | | | metal and glass, with active charge | | | balancing to preserve neural health | +-------------------+----------------------------------------------+ | life support | closed loop: temperature, CO2/O2/N2 gas mix, | | | media perfusion, waste filtration | +-------------------+----------------------------------------------+ | culture lifetime | up to ~6 months in the unit | +-------------------+----------------------------------------------+ | runtime | biOS — writes electrical stimuli to the | | | array, reads the response back, | | | sub-millisecond loop latency | +-------------------+----------------------------------------------+ | power draw | under 1 kW for a full rack of units | +-------------------+----------------------------------------------+ | availability | $35,000 per unit, or remote access as | | | wetware-as-a-service | +-------------------+----------------------------------------------+ | prior art | DishBrain (2022) — the same lineage of | | | cultures learned to play Pong in a closed | | | sensory loop | +-------------------+----------------------------------------------+
// figures as published by cortical labs and its press coverage. neuron counts quoted for cl1 vary between sources and between culture batches.
why anyone bothers: the array is a genuine closed loop. stimulation goes in, activity comes out, and the culture rewires in response to what it gets. learning here is not backpropagation over a loss — it is synaptic plasticity in wet tissue, running at roughly the power budget of a lightbulb.
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