Strategy to improve the quantitative LC-MS analysis of molecular ions resistant to gas-phase collision induced dissociation: application to disulfide-rich cyclic peptides.

Due to observed collision induced dissociation (CID) fragmentation inefficiency, developing sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) assays for CID resistant compounds is especially challenging. As an alternative to traditional LC-MS/MS, we present here a methodology that preserves the intact analyte ion for quantification by selectively filtering ions while reducing chemical noise. Utilizing a quadrupole-Orbitrap MS, the target ion is selectively isolated while interfering matrix components undergo MS/MS fragmentation by CID, allowing noise-free detection of the analyte's surviving molecular ion. In this manner, CID affords additional selectivity during high resolution accurate mass analysis by elimination of isobaric interferences, a fundamentally different concept than the traditional approach of monitoring a target analyte's unique fragment following CID. This survivor-selected ion monitoring (survivor-SIM) approach has allowed sensitive and specific detection of disulfide-rich cyclic peptides extracted from plasma.

[1]  R. Cooks,et al.  Orbitrap mass spectrometry: instrumentation, ion motion and applications. , 2008, Mass spectrometry reviews.

[2]  Nuno Bandeira,et al.  Interpretation of tandem mass spectra obtained from cyclic nonribosomal peptides. , 2009, Analytical chemistry.

[3]  W. Hendrickson,et al.  A structural superfamily of growth factors containing a cystine knot motif , 1993, Cell.

[4]  David J. Craik,et al.  Seamless Proteins Tie Up Their Loose Ends , 2006, Science.

[5]  William DeMaio,et al.  Spectral accuracy of molecular ions in an LTQ/Orbitrap mass spectrometer and implications for elemental composition determination , 2009, Journal of the American Society for Mass Spectrometry.

[6]  Albert J R Heck,et al.  Improving SRM assay development: a global comparison between triple quadrupole, ion trap, and higher energy CID peptide fragmentation spectra. , 2011, Journal of proteome research.

[7]  W. Lambert,et al.  Adduct formation in quantitative bioanalysis: Effect of ionization conditions on paclitaxel , 2004, Journal of the American Society for Mass Spectrometry.

[8]  S. A. McLuckey Principles of collisional activation in analytical mass spectrometry , 1992, Journal of the American Society for Mass Spectrometry.

[9]  Petia Shipkova,et al.  Application of ion trap technology to liquid chromatography/mass spectrometry quantitation of large peptides. , 2008, Rapid communications in mass spectrometry : RCM.

[10]  F. Engler,et al.  Electron transfer dissociation coupled to an Orbitrap analyzer may promise a straightforward and accurate sequencing of disulfide-bridged cyclic peptides: a case study. , 2010, Journal of mass spectrometry : JMS.

[11]  D. Mckenzie,et al.  High-throughput bioanalysis of bile acids and their conjugates using UHPLC coupled to HRMS. , 2013, Bioanalysis.

[12]  Derek J. Bailey,et al.  Parallel Reaction Monitoring for High Resolution and High Mass Accuracy Quantitative, Targeted Proteomics* , 2012, Molecular & Cellular Proteomics.

[13]  D. Craik,et al.  Disulfide-rich macrocyclic peptides as templates in drug design. , 2014, European journal of medicinal chemistry.

[14]  N. Neamati,et al.  In vivo activation of the p53 tumor suppressor pathway by an engineered cyclotide. , 2013, Journal of the American Chemical Society.

[15]  S. A. McLuckey,et al.  Collision-induced dissociation (CID) of peptides and proteins. , 2005, Methods in enzymology.

[16]  D J Crouch,et al.  Determination of buprenorphine in human plasma by gas chromatography-positive ion chemical ionization mass spectrometry and liquid chromatography-tandem mass spectrometry. , 1997, Journal of analytical toxicology.

[17]  Fabio Garofolo,et al.  Large-molecule quantification: sensitivity and selectivity head-to-head comparison of triple quadrupole with Q-TOF. , 2013, Bioanalysis.

[18]  D. Craik,et al.  The cystine knot motif in toxins and implications for drug design. , 2001, Toxicon : official journal of the International Society on Toxinology.

[19]  B. Domon,et al.  Targeted Proteomic Quantification on Quadrupole-Orbitrap Mass Spectrometer* , 2012, Molecular & Cellular Proteomics.

[20]  Julie H. Campbell,et al.  Engineering pro-angiogenic peptides using stable, disulfide-rich cyclic scaffolds. , 2011, Blood.