FoldToken2: Learning compact, invariant and generative protein structure language
This addresses the problem of protein structure representation, alignment, and generation for computational biology, with incremental improvements over previous work.
The paper tackled the challenge of creating a compact and invariant language for representing protein structures by proposing FoldToken2, which improved reconstruction performance by 20% in TMScore and 81% in RMSD compared to its predecessor.
The equivalent nature of 3D coordinates has posed long term challenges in protein structure representation learning, alignment, and generation. Can we create a compact and invariant language that equivalently represents protein structures? Towards this goal, we propose FoldToken2 to transfer equivariant structures into discrete tokens, while maintaining the recoverability of the original structures. From FoldToken1 to FoldToken2, we improve three key components: (1) invariant structure encoder, (2) vector-quantized compressor, and (3) equivalent structure decoder. We evaluate FoldToken2 on the protein structure reconstruction task and show that it outperforms previous FoldToken1 by 20\% in TMScore and 81\% in RMSD. FoldToken2 probably be the first method that works well on both single-chain and multi-chain protein structures quantization. We believe that FoldToken2 will inspire further improvement in protein structure representation learning, structure alignment, and structure generation tasks.