Afshar Bakshloo Mazdak, Yahiaoui Safia, Ouldali Hadjer, Pastoriza-Gallego Manuela, Piguet Fabien, Oukhaled Abdelghani
CY Cergy Paris Université, CNRS, LAMBE, Cergy, 95000, France.
Université Paris-Saclay, Univ Evry, CNRS, LAMBE, Evry-Courcouronnes, 91000, France.
Proteomics. 2022 Jun;22(11-12):e2100056. doi: 10.1002/pmic.202100056. Epub 2022 Apr 7.
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.
基于纳米孔的单分子分析技术是蛋白质组学领域一种很有前景的方法。在本技术简报中,研究了气单胞菌溶素(AeL)的生物纳米孔与肽之间的相互作用,重点关注取决于AeL激活方案的潜在偏差。我们的结果表明,在使用经典的AeL激活方案时,可能会无意中引入到分析物溶液中的残留胰蛋白酶,可通过对较长肽的酶促降解诱导较短肽的大量形成,这可能导致不良影响和/或错误解读。AeL无胰蛋白酶激活方案消除了这种偏差,似乎更适合肽/蛋白质分析,特别是从基于纳米孔的分子指纹识别或低丰度物种表征的角度来看。