Iterative correction of suppressed peptide profiles from FTMS measurements

Xuepo Ma, T. Hestilow, Jian Cui, Jianqiu Zhang
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Abstract

Analysis of peptide profiles from a Liquid Chromatography Fourier Transform Mass Spectrometry (LC/FTMS) measurement reveals a non-linear distortion in intensity. Investigation of the measured CVi /C12 ratios comparing with theoretical ones shows that the non-linearity can be attributed to low intensity signal suppression of low abundance peptide peaks. We find that the suppression is homogenous for different isotopes of identical peptides but non-homogenous for different peptides. We developed an iterative correction algorithm that corrects the intensity distortions for peptides with relatively high abundance. This algorithm can be applied in a wide range of applications using FTMS.
从FTMS测量抑制肽谱的迭代校正
从液相色谱傅立叶变换质谱(LC/FTMS)测量肽谱分析揭示了强度的非线性失真。实测的CVi /C12比值与理论值比较表明,非线性可归因于低丰度肽峰的低强度信号抑制。我们发现对相同多肽的不同同位素的抑制是均匀的,而对不同多肽的抑制是不均匀的。我们开发了一种迭代校正算法,用于校正相对较高丰度的肽的强度扭曲。该算法可广泛应用于FTMS的应用中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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