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Tucs, A.

Publications and source records attributed to Tucs, A..

2 recordsLinked to original sources

pLM-bVAE: protein language model-enhanced binary representation improves quantum annealing-based protein sequence design

Quantum annealing (QA) has been explored as an approach for protein design in vast combinatorial sequence spaces. Applying QA to protein sequence design requires amino acid sequences to be encoded as binary vectors, and optimized vectors to be decoded back into amino acid sequences. Thus, both the quality of binary encoding and sequence reconstruction accuracy are important for effective QA-based optimization. Binary variational autoencoder (bVAE) has been used to map protein sequences to binary representations in QA-based protein sequence design. However, bVAE was originally developed for natural language modeling, and its suitability for proteins has not been systematically evaluated. Here, we present pLM-bVAE, which incorporates protein representations derived from a pretrained protein language model (pLM) into the original bVAE model. In computational experiments on three public protein variant datasets, pLM-bVAE showed higher sequence reconstruction accuracy and binary encoding performance than bVAE. Moreover, we incorporated pLM-bVAE into a QA-based protein sequence design framework. Across all three datasets, pLM-bVAE generated more high-scoring sequences with greater sequence dissimilarity from the training and validation data than bVAE. Our results demonstrate that pLM-bVAE provides an effective binary representation for improving QA-based protein sequence design. Availability The source code used in this manuscript is available at https://github.com/hueda8/pLM-bVAE.

bioinformatics↗

Prefusion conformation of SARS-CoV-2 receptor-binding domain favors interactions with human receptor ACE2

A new coronavirus pandemic COVID-19, caused by Severe Acute Respiratory Syndrome coronavirus (SARS-CoV-2), poses a serious threat across continents, leading the World Health Organization to declare a Public Health Emergency of International Concern. In order to block the entry of the virus into human host cells, major therapeutic and vaccine design efforts are now targeting the interactions between the SARS-CoV-2 spike (S) glycoprotein and the human cellular membrane receptor angiotensin-converting enzyme, hACE2. By analyzing cryo-EM structures of SARS-CoV-2 and SARS-CoV-1, we report here that the homotrimer SARS-CoV-2 S receptor-binding domain (RBD) that binds with hACE2 has expanded in size, undergoing a large conformational change relative to SARS-CoV-1 S protein. Protomer with the up-conformational form of RBD, which binds with hACE2, exhibits higher intermolecular interactions at the RBD-ACE2 interface, with differential distributions and the inclusion of specific H-bonds in the CoV-2 complex. Further interface analysis has shown that interfacial water promotes and stabilizes the formation of CoV-2/hACE2 complex. This interaction has caused a significant structural rigidification, favoring proteolytic processing of S protein for the fusion of the viral and cellular membrane. Moreover, conformational dynamics simulations of RBD motions in SARS-CoV-2 and SARS-CoV-1 point to the role in modification in the RBD dynamics and their likely impact on infectivity.

bioinformatics↗