Potassium tetratitanate (K2Ti4O9) has been synthesized by solid state method using K2CO3 and TiO2, and studied as an anode material for potassium ion batteries for the first time. A discharge capacity of 80 mAh g−1 has been obtained at a current density of 100 mA g−1 (0.8 C rate) and 97 mAh g−1 at 30 mA g−1 (0.2 C rate), initially. The discharge capacity is stable at low rates of cycling. The uptake of K+ on charging K2Ti4O9 electrodes is quantitatively studied. The proposed mechanism of charging involves reduction of two Ti ions from 4+ oxidation state to 3+ oxidation state, which facilitates insertion of two K+ ions per formula unit. The rate capability experiments suggest that K2Ti4O9 is capable of undergoing charge-discharge cycling at high rates (up to 15 C rate), but with a low discharge capacity. Thus K2Ti4O9 is a promising anode material for future K-ion batteries.
Motivation
Accurate prediction of binding between a major histocompatibility complex (MHC) allele and a peptide plays a major role in the synthesis of personalized cancer vaccines. The immune system struggles to distinguish between a cancerous and a healthy cell. In a patient suffering from cancer who has a particular MHC allele, only those peptides that bind with the MHC allele with high affinity, help the immune system recognize the cancerous cells.
Results
MHCAttnNet is a deep neural model that uses an attention mechanism to capture the relevant subsequences of the amino acid sequences of peptides and MHC alleles. It then uses this to accurately predict the MHC-peptide binding. MHCAttnNet achieves an AUC-PRC score of 94.18% with 161 class I MHC alleles, which outperforms the state-of-the-art models for this task. MHCAttnNet also achieves a better F1-score in comparison to the state-of-the-art models while covering a larger number of class II MHC alleles. The attention mechanism used by MHCAttnNet provides a heatmap over the amino acids thus indicating the important subsequences present in the amino acid sequence. This approach also allows us to focus on a much smaller number of relevant trigrams corresponding to the amino acid sequence of an MHC allele, from 9251 possible trigrams to about 258. This significantly reduces the number of amino acid subsequences that need to be clinically tested.
Availability and implementation
The data and source code are available at https://github.com/gopuvenkat/MHCAttnNet.
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