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Biology subjects

Aylott, J. W.

Publications and source records attributed to Aylott, J. W..

2 recordsLinked to original sources

Fluorescent pH-sensitive nanosensors enable precise low-volume monitoring in high-throughput bioprocess manufacturing

Abstract / SummaryBiopharmaceutical manufacturing requires precise pH control during production to ensure product quality and process performance. However, achieving this precision in low-volume, high-throughput automated settings present significant challenges with existing technology, often leading to inefficiencies and inaccuracies. This study introduces fluorescent nanosensors as a novel solution for accurate pH monitoring in micro-scale environments. Employing ratiometric fluorescence measurement, these nanosensors use analyte responsive and reference fluorophores in inert polyacrylamide matrices to perform dynamic measurements over pH 3.5 - 7.5. Nanosensors (35.26 {+/-} 3.66 nm diameter) were synthesised with a neutral or positive surface charge (-5.08 {+/-} 4.05 mV and +12.87 {+/-} 1.25 mV, respectively). An automated workflow, using sacrificial and at line sample analysis, was developed by integrating the nanosensors with a TECAN automated liquid handling platform and a fluorescence spectrophotometer. The method was verified using in-process samples obtained from a monoclonal antibody purification, to highlight the compatibility of the nanosensors to different buffer systems in a typical biopharmaceutical manufacturing process. We show that pH-sensitive nanosensors can effectively monitor pH through the various stages of purification, demonstrating high accuracy (pH {+/-} 0.23-0.40) even in sample volumes as low as 12.5 L. The application of nanosensors represents a significant advancement in high-throughput scale-down bioprocess development by enabling precise, automated pH adjustment. This study improves the understanding of biopharmaceutical manufacturing, through the application of fluorescent nanosensors, paving-the-way for optimisations in low-volume and high-throughput product production. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=77 SRC="FIGDIR/small/612862v1_ufig1.gif" ALT="Figure 1"> View larger version (23K): org.highwire.dtl.DTLVardef@1fe2ef1org.highwire.dtl.DTLVardef@bbf524org.highwire.dtl.DTLVardef@1db0edcorg.highwire.dtl.DTLVardef@aca81c_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioengineering↗

In situ protein identification and mapping using secondary ion mass spectrometry

Protein characterisation at surfaces currently requires digestion prior to either liquid extraction of the protein for mass spectrometry analysis or in situ matrix-assisted desorption/ionisation. Here, we show that direct assignment of individual proteins and mixtures at surfaces can be achieved by employing secondary ion mass spectrometry (SIMS) with gas cluster ion beam (GCIB) bombardment and an Orbitrap analyser. Potential applications of the method are illustrated by demonstrating imaging of a protein film masked by a gold grid and the analysis of a protein monolayer biochip.

biochemistry↗