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Biology subjects

Kakhaki, P. D.

Publications and source records attributed to Kakhaki, P. D..

3 recordsLinked to original sources

A strategy for ionic current analysis of nanopore protein readouts

BackgroundNanopore-based protein reading holds promise for single-molecule proteomics, but analyzing the resulting ionic current signals presents substantial computational challenges. Unlike nucleic acids, peptide-associated ionic signals exhibit complex patterns with subtle transitions between amino acids that can be obscured by noise. We developed an integrated computational strategy for processing nanopore protein ionic current signals from synthetic protein constructs containing all 20 amino acids in controlled sequence contexts. We started with denoising to remove artifacts, followed by change point detection using variable-number and fixed-number segmentation methods. ResultsWe employed dynamic time warping barycenter averaging to generate amino acid-specific reference templates. In parallel, we performed classification of amino acid regions using bidirectional LSTM networks trained on segment-level statistical features. Accuracy for 20-way amino acid classification remained limited, while charge-based binary classification reached 93.3% accuracy. Pairwise classification revealed that certain amino acids, particularly negatively charged residues, generate distinctive signatures. We used a profile hidden Markov model to capture sequential structure of protein translocation. ConclusionThis approach provides computational strategies for automated segmentation, classification, and modeling of nanopore peptide translocation ionic current data.

bioinformatics↗

Intact and single-molecule analysis of heparan sulfate

Establishing tools to couple biological processes to a DNA sequence has transformed our ability to monitor life at the molecular scale due to the scalability, flexibility, and low cost of DNA sequencing. Key examples include DNA-protein (ChIP-seq1), RNA-protein (CLIP-seq2), protein-protein (proximity ligation assay3), and Cas-based recording of cellular events4. In contrast, this paradigm has not yet significantly enhanced studies of glycans, which are mostly limited to non-DNA based chemical and biochemical assays. While classical asparagine-linked and serine/threonine-linked glycans can be directly sequenced using mass spectrometry, glycosaminoglycans - notable players in the extracellular matrix - cannot be easily analyzed in their full-length form. Here we introduce HS-nano-seq, a generalized framework to selectively label, process, and detect features of heparan sulfate on a nanopore sequencing platform. Recognizing that heparan sulfate is biochemically analogous to a nucleic acid, we report purification techniques using rapid nucleic acid strategies and conjugation methods to couple DNA adapters, generating HS-DNA chimeras resolved as discrete species by capillary electrophoresis (CE). The CE assay can distinguish features of chain length and sulfation patterns. At the single-molecule level enabled by nanopore sensing, we classify a library of synthetic heparan sulfate standards and demonstrate that nanopore ionic current fingerprints encode sulfation-dependent structural features of individual HS chains. Analysis of intact, cell-derived HS could discriminate features of individual chains with different sulfation patterns, defining the heterogeneity of binding motifs across cell types and how cells organize and program the tethered extracellular matrix. More broadly, HS-nano-seq establishes a framework for achieving full-length readouts of ECM glycopolymers that are amenable to the same biological interrogation as nucleic acids.

biochemistry↗

tRNA isodecoder analysis using Nanopore ionic current signals and deep learning

tRNA are short non-coding RNA characterized by their distinct tertiary structure and abundant chemical modifications. Conventional analysis strategies do not fully characterize tRNA isodecoders. We demonstrate that this limitation can be resolved for tRNA using nanopore ionic current data. We developed tRNAZAP, a deep learning strategy that uses nanopore ionic current signal information to classify native tRNA strands at isodecoder-level resolution without relying on sequence information. Additionally, the ionic current level classification allows for pairwise alignment of read sequences to reference sequences, producing optimal tRNA alignments. We applied tRNAZAP to direct tRNA sequencing data from Escherichia coli and Saccharomyces cerevisiae, and recovered 2.6% and 13.1% more aligned reads than BWA-MEM, respectively. tRNAZAP resolved these reads at an isodecoder-level and with consistently higher alignment identity. tRNAZAP is a powerful complement to sequence-based profiling and can contribute towards resolving the isodecoder landscape in more complex organisms including humans.

genomics↗