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Biology subjects

Yanai, G.

Publications and source records attributed to Yanai, G..

3 recordsLinked to original sources

Coarse-tuning to improve a protein foundation model for a domain of proteins: the example of outer membrane beta barrels

Foundation models for proteins have shown great potential in addressing a wide range of challenges in computational molecular biology. State-of-the-art models are trained on large and diverse corpora of protein sequences, enabled by self-supervised training. The models are then used in transfer learning and the embeddings they calculate are used in supervised downstream tasks. We propose a novel focusing mechanism for foundation models, which we call 'coarse-tuning'. In coarse-tuning, we further update the model, using a defined yet unlabeled, dataset to enhance its performance in a specific domain. We demonstrate this approach using Outer Membrane Beta Barrels (OMBBs) - proteins that are found in the distinct biophysical environment of the outer membrane. Our results show that coarse-tuned models outperform the original foundation model when applied to various transfer learning tasks. Additionally, we study the embeddings generated by the coarse-tuned models and compare them to those from the original foundation model, including an investigation of the learned attention matrices via contact map predictions. Our work suggests that a medium-sized dataset (fewer than 100,000 protein sequences) is sufficient to effectively specialize a foundation model to a specific domain, enhancing its utility for domain-specific applications.

molecular biology↗

Contrastive learning unites sequence and structure in a global representation of protein space

Amino acid sequence dictates the three-dimensional structure and biological function of proteins. Yet, despite decades of research, our understanding of the interplay between sequence and structure is incomplete. To meet this challenge, we introduce Contrastive Learning Sequence-Structure (CLSS), an AI-based contrastive learning model trained to co-embed sequence and structure information in a self-supervised manner. We trained CLSS on large and diverse sets of protein building blocks called domains. CLSS represents both sequences and structures as vectors in the same high-dimensional space, where distance relates to sequence-structure similarity. Thus, CLSS provides a natural way to represent the protein universe, reflecting evolutionary relationships, as well as structural changes. We find that CLSS refines expert knowledge about the global organization of protein space, and highlights transitional forms that resist hierarchical classification. CLSS reveals linkage between domains of seemingly separate lineages, thereby significantly improving our understanding of evolutionary design.

bioinformatics↗

Natural and age-related variation in circulating human hematopoietic stem cells

Hematopoietic stem and progenitor cells (HSPCs) deliver life-long multi-lineage output. However, with aging, we exhibit certain characteristic blood count changes and accumulation of clonal disorders. Better understanding of inter-individual variation in HSPC behavior is needed to understand these age-related phenomena and the transition from health to chronic and acute hematological malignancies. Here we study 627K single circulating CD34+ HSPCs (cHSPCs) from 148 healthy individuals, along with their clinical information and clonal hematopoiesis (CH) profiles, to characterize population-wide and age-related hematopoietic variability. Individuals with CH were linked with reduced frequencies of lymphocyte progenitors and higher RDW. An age-related decrease in lymphoid progenitors was observed, predominantly in males. Inter-individual transcriptional variation in expression of a Lamin-A signature and stemness gene programs were linked with aging and presence of macrocytic anemia. Based on our model for healthy cHSPC variation we construct the normal reference for cHSPC subtype frequencies. We show how compositional and expression deviations from this normal reference can robustly identify myeloid malignancies and pre-malignant states. Together, our data and methodologies present a novel resource, shedding light on various age-related hematopoietic processes, and a comprehensive normal cHSPC reference, which can serve as a tool for diagnosing and characterizing hematological disorders.

molecular biology↗