Bio papers — 2026-09-15

The AbFlow framework introduces a one-step flow-matching method for designing full-atom antibodies end-to-end by using paratope restrictions to guide the process. This approach refines antibody structures, particularly the CDRH3 region, by using an extended velocity field network enhanced by an equivariant surface multi channel encoder that takes surface interaction data as input. This method produces superior antigen antibody complexes and markedly improves binding affinity compared to previous designs.

This success builds on earlier work that focused on optimizing binding affinity through different structural modeling techniques. Stable-Shift addresses the challenge of predicting how genes will respond to genetic changes in ways not seen before, which is important for reducing the need for expensive functional genomics experiments. It achieves this by aggregating single cell measurements into perturbation level expression shifts and fitting a low rank response basis using only training perturbations.

This prediction method achieved a cosine similarity of 0.592 on the K562 Perturb-seq benchmark, outperforming GEARS at 0.569. Furthermore, it showed better correlation with biological context inputs like STRING interactions and Gene Ontology annotations. This suggests that structuring the response prediction based on known biological networks helps capture unseen gene behavior more accurately than methods relying solely on raw data.

We also looked at how models can communicate complex perceptual experiences without changing their core meaning using the Perceptual Reality Transformer, which keeps source accounts alongside generated illustrations. Studies showed that while frozen neural representations can predict complex content well with an AUROC of 0.887 to 0.894, recovering subjective qualities like vividness and persistence is more difficult than predicting the content itself.

Finally, we explored how recurrent neuronal networks in the hippocampus achieve optimal goal-directed navigation through relaxation dynamics instead of explicit planning algorithms. This network learns transition probabilities between spatial locations where obstacles are represented by vanishing connection weights. When a goal is presented, the dynamics relax into a field equivalent to a Linearly solvable Markov Decision Process.

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Important terms

AbFlow
This framework is a one-step flow-matching method for designing complete antibodies from start to finish by using paratope restrictions to steer the process. It refines antibody structures, especially the CDRH3 region, leading to better antigen antibody complexes and stronger binding affinity.
Stable-Shift
This method predicts how genes will react to genetic changes in novel ways without needing costly functional genomics experiments. It does this by grouping single cell data into expression shifts and fitting a low-rank response basis.
Perceptual Reality Transformer
This model communicates complex experiences, like illustrations, while preserving the original meaning of the source accounts. It shows that predicting content is possible, but capturing subjective qualities like vividness is harder.
Recurrent neuronal networks
These networks in the hippocampus achieve goal-directed navigation by relaxing into specific dynamics rather than using explicit planning. They learn movement probabilities between locations where obstacles are represented by weak connections.