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Simmel, F.

Publications and source records attributed to Simmel, F..

2 recordsLinked to original sources

Systematic non-natural base-pairs for strand displacement circuits in complex environments

Nucleic acid strand displacement (SD) circuits have enabled impressive realizations of molecular computing in vitro, but operating them in contention with competing reaction pathways can cause signal leak and circuit failure. Further, operating SD circuits in complex environments, ranging from pools of nucleic acids to living organisms, can exacerbate these challenges. To address these issues, we explore the incorporation of isoC and isoG non-natural bases in single- and multi-step SD cascades and started by studying their promiscuity. We combined the non-natural bases with a mismatch strategy, showing them to be fully compatible. The synthesis we show between strategic placement of non-natural bases and systematic mismatch optimization of SD circuits offers a design space for future circuits that are fast, robust, and biologically compatible. Comparing circuit slowdowns by random pool backgrounds in the presence and absence of non-natural base pairs reveals a significant difference. Using isoC:isoG base pairs in the toehold region shows the greatest effect, with some further positive effects caused by additional non-natural bases in the branch migration domain. Such insights will pave the way for developing SD circuits that operate in complex environments, expanding the applications of molecular computing in a wider range of scenarios.

bioengineering↗

High Performance protocol for ultra-short DNA sequencing using Oxford Nanopore Technology (ONT)

In recent years, Oxford Nanopore Technologies (ONT) has gained substantial attention across various domains of nucleic acids research, owing to its unique advantages over other sequencing platforms. Originally developed for long-read sequencing, ONT technology has evolved, with recent advancements enhancing its applicability beyond long reads to include short, synthetic DNA-based applications. However, sequencing short DNA fragments with nanopore technology often results in lower data quality, likely due to a lack of protocols optimised for these fragment sizes. To address this challenge, we refined the standard ONT library preparation protocol to improve its performance for ultra-short DNA targets. Utilising the same core reagents required for conventional ONT workflows, we introduced targeted alterations to enhance compatibility with shorter fragment lengths. We then benchmarked these adjustments against libraries prepared using the standard ONT protocol. Here, we present a comprehensive, step-by-step protocol that is accessible to researchers of varied technical expertise, facilitating high-quality sequencing of ultra-short DNA fragments. This protocol represents a significant improvement in sequencing quality for short DNA fragments using ONT technology, broadening the range of possible applications. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=167 SRC="FIGDIR/small/632410v1_ufig1.gif" ALT="Figure 1"> View larger version (40K): org.highwire.dtl.DTLVardef@1c99f4eorg.highwire.dtl.DTLVardef@1f9cf50org.highwire.dtl.DTLVardef@199c8acorg.highwire.dtl.DTLVardef@1459f48_HPS_FORMAT_FIGEXP M_FIG C_FIG

molecular biology↗