Literature DB >> 33174564

Nanopore sensing of single-biomolecules: a new procedure to identify protein sequence motifs from molecular dynamics.

Adrien Nicolaï1, Aniket Rath, Patrice Delarue, Patrick Senet.   

Abstract

Solid-state nanopores have emerged as one of the most versatile tools for single-biomolecule detection and characterization. Nanopore sensing is based on the measurement of variations in ionic current as charged biomolecules immersed in an electrolyte translocate through nanometer-sized channels, in response to an external voltage applied across the membrane. The passage of a biomolecule through a pore yields information about its structure and chemical properties, as demonstrated experimentally with sub-microsecond temporal resolution. However, extracting the sequence of a biomolecule without the information about its position remains challenging due to the fact there is a large variability of sensing events recorded. In this paper, we performed microsecond time scale all-atom non-equilibrium Molecular Dynamics (MD) simulations of peptide translocation (motifs of alpha-synuclein, associated with Parkinson's disease) through single-layer MoS2 nanopores. First, we present an analysis based on the current threshold to extract and characterize meaningful sensing events from ionic current time series computed from MD. Second, a mechanism of translocation is established, for which side chains of each amino acid are oriented parallel to the electric field when they are translocating through the pore and perpendicular otherwise. Third, a new procedure based on the permutation entropy (PE) algorithm is detailed to identify protein sequence motifs related to ionic current drop speed. PE is a technique used to quantify the complexity of a given time series and it allows the detection of regular patterns. Here, PE patterns were associated with protein sequence motifs composed of 1, 2 or 3 amino acids. Finally, we demonstrate that this very promising procedure allows the detection of biological mutations and could be tested experimentally, despite the fact that reconstructing the sequence information remains unachievable at this time.

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Year:  2020        PMID: 33174564     DOI: 10.1039/d0nr05185c

Source DB:  PubMed          Journal:  Nanoscale        ISSN: 2040-3364            Impact factor:   7.790


  1 in total

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

Authors:  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:  iScience       Date:  2021-12-11
  1 in total

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