iScience (Jan 2022)

ProtSeq: Toward high-throughput, single-molecule protein sequencing via amino acid conversion into DNA barcodes

  • Jessica M. Hong,
  • Michael Gibbons,
  • Ali Bashir,
  • Diana Wu,
  • Shirley Shao,
  • Zachary Cutts,
  • Mariya Chavarha,
  • Ye Chen,
  • Lauren Schiff,
  • Mikelle Foster,
  • Victoria A. Church,
  • Llyke Ching,
  • Sara Ahadi,
  • Anna Hieu-Thao Le,
  • Alexander Tran,
  • Michelle Dimon,
  • Marc Coram,
  • Brian Williams,
  • Phillip Jess,
  • Marc Berndl,
  • Annalisa Pawlosky

Journal volume & issue
Vol. 25, no. 1
p. 103586

Abstract

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Summary: We demonstrate early progress toward constructing a high-throughput, single-molecule protein sequencing technology utilizing barcoded DNA aptamers (binders) to recognize terminal amino acids of peptides (targets) tethered on a next-generation sequencing chip. DNA binders deposit unique, amino acid-identifying barcodes on the chip. The end goal is that, over multiple binding cycles, a sequential chain of DNA barcodes will identify the amino acid sequence of a peptide. Toward this, we demonstrate successful target identification with two sets of target-binder pairs: DNA-DNA and Peptide-Protein. For DNA-DNA binding, we show assembly and sequencing of DNA barcodes over six consecutive binding cycles. Intriguingly, our computational simulation predicts that a small set of semi-selective DNA binders offers significant coverage of the human proteome. Toward this end, we introduce a binder discovery pipeline that ultimately could merge with the chip assay into a technology called ProtSeq, for future high-throughput, single-molecule protein sequencing.

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