On possible trypsin-induced biases in peptides analysis with aerolysin nanopore

被引:6
作者
Afshar Bakshloo, Mazdak [1 ,2 ]
Yahiaoui, Safia [1 ,2 ]
Ouldali, Hadjer [1 ,2 ]
Pastoriza-Gallego, Manuela [1 ,2 ]
Piguet, Fabien [1 ,2 ]
Oukhaled, Abdelghani [1 ,2 ]
机构
[1] CY Cergy Paris Univ, CNRS, LAMBE, F-95000 Cergy, France
[2] Univ Evry, Univ Paris Saclay, CNRS, LAMBE, F-91000 Evry, France
关键词
aerolysin; enzymatic degradation; low-abundance; nanopore; peptides; MEMBRANE-CHANNEL; PROTEIN; PORE;
D O I
10.1002/pmic.202100056
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nanopore-based single-molecule analysis technique is a promising approach in the field of proteomics. In this Technical Brief, the interaction between the biological nanopore of Aerolysin (AeL) and peptides is investigated, focusing on potential biases depending on the AeL activation protocol. Our results reveal that residual trypsin, which may be unintentionally introduced in analyte solution when using a classical AeL activation protocol, can induce a significant formation of shorter peptides by enzymatic degradation of longer ones, which may lead to unwanted effects and/or misinterpretations. AeL free-trypsin activation protocol eliminates this bias and appears more appropriate for peptide/proteins analysis, specifically in the perspective of nanopore-based molecular fingerprinting or of low-abundance species characterization.
引用
收藏
页数:8
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