Identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 29511176.
- Also identified by DOI 10.1038/s41467-018-03418-2 and PMC identifier 5840376.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
There are still unmet needs in finding new technologies for biomedical diagnostic and industrial applications. A technology allowing the analysis of size and sequence of short peptide molecules of only few molecular copies is still challenging. The fast, low-cost and label-free single-molecule nanopore technology could be an alternative for addressing these critical issues. Here, we demonstrate that the wild-type aerolysin nanopore enables the size-discrimination of several short uniformly charged homopeptides, mixed in solution, with a single amino acid resolution. Our system is very sensitive, allowing detecting and characterizing a few dozens of peptide impurities in a high purity commercial peptide sample, while conventional analysis techniques fail to do so.
Medical subject headings
- Bacterial Toxins
- Peptides
- Pore Forming Cytotoxic Proteins