MRCQuant- an accurate LC-MS relative isotopic quantification algorithm on TOF instruments
© Haskins et al; licensee BioMed Central Ltd. 2011
Received: 29 July 2010
Accepted: 15 March 2011
Published: 15 March 2011
Relative isotope abundance quantification, which can be used for peptide identification and differential peptide quantification, plays an important role in liquid chromatography-mass spectrometry (LC-MS)-based proteomics. However, several major issues exist in the relative isotopic quantification of peptides on time-of-flight (TOF) instruments: LC peak boundary detection, thermal noise suppression, interference removal and mass drift correction. We propose to use the Maximum Ratio Combining (MRC) method to extract MS signal templates for interference detection/removal and LC peak boundary detection. In our method, MRCQuant, MS templates are extracted directly from experimental values, and the mass drift in each LC-MS run is automatically captured and compensated. We compared the quantification accuracy of MRCQuant to that of another representative LC-MS quantification algorithm (msInspect) using datasets downloaded from a public data repository.
MRCQuant showed significant improvement in the number of accurately quantified peptides.
MRCQuant effectively addresses major issues in the relative quantification of LC-MS-based proteomics data, and it provides improved performance in the quantification of low abundance peptides.
The large-scale identification, characterization and quantification of proteins in biological samples by liquid chromatography-mass spectrometry (LC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based proteomic methods play a crucial role in biomedical research [1, 2]. For example, in biomarker discovery studies, a common aim is to elucidate a set of proteins that can be used to reliably differentiate diseased and normal samples by abundance measurements. Precision and accuracy are critical for confident protein biomarker discovery and validation. In "bottom-up" approaches, proteins are cleaved by sequence-specific proteases such as trypsin prior to analysis. A protein fold change can be inferred from the relative abundance of peptides across samples, where peptide identification and quantification can be accomplished in separate steps . In this paper, we consider the problem of relative isotopic quantification of peptides in LC-MS based on time-of-flight (TOF) instruments. It is assumed herein that a list of candidate peptides has been compiled a priori, and that we are interested in measuring the relative abundance of their isotopes (natural or labeled).
The measurement of peptide abundance is complicated by the fact that a peptide forms both LC and MS peaks during its LC elution interval. To quantify a peptide, it requires the integration of its complete LC peaks, which is sometimes impossible due to strong interference from other peptide species or contaminants. However, relative quantification is still possible for the uncorrupted segments of LC peaks with slightly different isotopic compositions. Relative isotope abundance measurement is particularly important in chemical and metabolic labeling experiments for the quantification of differential expression of isotopically-labeled peptide pairs and their corresponding proteins. In "label-free" LC-MS peptide detection, measurement of relative natural isotope abundance is employed for peptide detection. In both cases, there exist several significant challenges: 1. The determination of LC peak boundaries to exclude noisy scans; 2. Background noise suppression in LC peaks; 3. Interference detection and removal; and 4. Mass drift correction. To achieve accurate relative quantification, these issues have to be addressed. Current software packages have not addressed these issues effectively. QUIL  and ProteinQuant  determine LC peak boundaries by the apex and the full-width-half-maximum (FWHM) of a peak, i.e., it is assumed that for a given LC elution peak, the distance between its starting point and its apex is the FWHM of the peak. This assumption is problematic when elution peaks (especially low abundance ones) are asymmetrical and jagged. Some software packages use an intensity threshold or local minima to determine the boundaries of LC peaks. The main problem of these methods is: one is never sure whether noise or interference-corrupted scans are included within the peak boundaries, which could greatly degrade quantification accuracy. Among popular software packages, msInspect  and SuperHirn  use thresholds, ASAPRatio  and MapQuant  use peak apex and FWHM. Recently, MaxQuant  uses local minima for LC peak detection after Extracted-Ion-Chromatogram (XIC) smoothing. See  for a comprehensive review of software tools currently available for LC-MS quantification.
On the problem of background noise suppression, almost all current software packages use Savitzky-Golay or other types of filters [6, 8, 10] to smooth XICs. However, through our own observation, elution process variations share similar frequency characteristics with that of instrument and Poisson noise (see [Additional file 1] for a detailed description of this phenomenon). Applying filters will distort elution process variations which adversely affect quantification accuracy.
For interference detection and removal, most software packages de-convolute peptide peaks and only consider peak centroids. Although this procedure decouples peptides with similar masses to a degree, it is susceptible to thermal noise, which can cause errors in the calculation of peak centroids. In addition, this procedure cannot provide interference detection, which is critical for accurate quantification.
Also, automatic mass drift correction is not implemented in these software packages, and users are generally expected to supply mass calibration information. This requirement introduces another source of variability, since the accurate determination of mass drift over all m/z ranges is a challenging problem. These issues become more severe when peptide abundance is low. Consequently, they have been bottlenecks in quantitative proteomic studies. For example, it is observed that whenever the signal intensity is low, the measurement of isotopically-labeled peptide pairs tends to be erroneous . If we can computationally improve the coverage of accurate quantification, the chance for protein biomarker discovery will improve accordingly.
We limit the scope of this paper to TOFMS instruments where the Gaussian additive thermal noise model is appropriate [12, 13], (note that this is different from the Poisson plus multinomial noise model for the XICs). In contrast, in FTMS, the assumption of Gaussian additive noise does not hold which is noted in  as the phenomenon of increased noise in XICs.
In this paper, we propose a Maximum Ratio Combining (MRC) based Quantification (MRCQuant) algorithm to address current issues in quantification. MRCQuant was developed based on the observation that peptide species register identical MS peak signals (scaled and noise corrupted) in different MS scans and m/z locations. Sometimes, the registered peaks have high Signal-to-Noise ratios (SNRs), while in other occasions, the peaks are noisy with low SNRs. While quantification at high SNRs is very accurate, quantification at low SNRs is problematic due to noise. We can extract the Maximum Likelihood estimate of peptide MS signals from MS peaks at high SNRs using MRC, hence referred to as MS templates. Note that these templates are extracted directly from experiment, and are not "predefined", thus they can capture slight variations in the shape and center locations of MS peaks caused by different environmental factors and instrument designs. Subsequently, extracted MS templates can be used as references when quantifying low SNR peaks. This method can effectively remove background noise without filtering out elution process variations. In addition, extracted MS templates can be compared to MS peaks for interference detection and removal. After interference and noise removal, accurate quantification can be performed.
MRCQuant provides measurements of isotopic abundance for each peptide of interest at all charge states and all isotope positions of interest. The output of the algorithm can be further processed to infer relative protein abundance in labeled experiments, or the results can be used for peptide detection based on isotope pattern in LC-MS data. The peptide list of interest can be compiled from peptides identified from multiple LC-MS/MS runs or from LC-MS peak detection algorithms such as msInspect .
Maximum Ratio Combining (MRC) is an averaging method that has been widely applied in Telecommunications  for estimating the actual transmitted signal from multiple copies received through Additive White Gaussian Noise (AWGN) channels. MRC assigns averaging weights proportional to the square root of SNRs of received copies. MRC is mathematically derived based on the Maximum Likelihood principle. MRC provides an estimation of the transmitted signal with the highest SNR possible among all averaging methods. Given a peptide, we consider its MS peaks in multiple MS scans as copies of its real MS signal, which can be optimally estimated through MRC.
A reference template, not specific to any particular peptide, is defined as an estimation of the general MS peak shape in an LC-MS experiment. Such a peak shape is usually determined by instrument characteristics and environmental factors. Slight variations could exist between a reference template and particular peptide peak. This template can be translated and adjusted (in width) to different mass/charge (m/z) locations. (See support information for details of template translation). A reference template is described by its center m/z and its m/z -intensity pair values. Reference templates can either be extracted from LC-MS datasets at high SNRs, or can be theoretically predicted based on instrument resolution and characteristics. There may be several reference templates at different m/z values in an LC-MS dataset.
A peptide template is defined as an estimation of the MS peak signal registered by a specific peptide in one experiment. Comparing to reference templates, peptide templates are better estimations of MS peak signals for individual peptides. Peptide templates are generally extracted from MS peaks registered at the highest (most abundant) isotope and charge state position of peptides, where SNRs are high. Each peptide has its own template.
Here we describe the MRCQuant algorithm for relative peptide isotope quantification on LC-MS. The input of the algorithm includes an LC-MS dataset and a list of peptides to be quantified annotated by their monoisotopic mass and/or amino acid sequence. The mass annotation can be obtained through an LC-MS peptide identification algorithm like msInspect. The output of the algorithm is a matrix of abundance measurements, with a maximum of P columns, where P is the total number of peptides to be quantified, and whose rows are indexed by cs * maxcs + iso, where cs ∈ [1, maxcs] represents charge state, maxcs is the maximum number of charge states considered, and iso represents the isotope position. For a given peptide, we need to first detect its LC peaks. A peptide at a given mass forms a series of 2 D peptide peaks at different isotope and charge state positions. These 2 D peaks form LC and MS peaks if they are viewed from the elution time and m/z dimension. To establish the connection between a group of 2 D peaks to a specific peptide mass, we need to verify that: 1. their LC peaks at different isotope and charge state positions should be the same; and 2. their MS peaks match a reference template translated to their expected m/z locations. After LC peak identification, we need to accurately detect LC peak boundaries and perform quantification. To accomplish these goals, the proposed algorithm performs the following: 1. Extracts or theoretically predicts reference templates. 2. For each peptide of interest, performs LC peak detection at its highest isotope and charge state position using a reference template. 3.
Extracts peptide templates based on the MRC principle, which are used for accurate LC peak boundary detection and interference/noise removal at lower SNRs. Finally, quantification is performed based on peptide templates. The goal of the algorithm is to record accurate relative ion counts at all charge states and isotope positions.
Generation of reference templates
Reference templates can either be extracted from experiments directly, or obtained through theoretical prediction. Theoretically predicted templates can adopt different peak shapes according to different instrument characteristics (resolution for example). Mass drifts can be accounted by shifting the center of theoretically predicted templates according to mass calibrations. Next, we discuss in detail how to extract reference templates from LC-MS data at high SNRs. Given an input peptide list, we select a subset of peptide that register uncorrupted MS peaks, from which we extract a number of reference templates centered at different m/z values. The underlying assumption is that MS peaks registered by the same instrument should be similar (except that MS peaks are scaled both in m/z and intensity). Thus, it is possible to use the estimated MS peak signals at high SNRs as reference templates for initial LC peak detection. Note that slight deviation of actual MS signals to reference templates is allowed since the templates are used for LC peak detection but not quantification. The number of templates can be selected by the user, and 4 templates have been used in our simulations with good results. Later, when quantifying a peptide at a given m/z value, we will not use a reference template, instead, we will use a peptide template for accurate quantification at low SNRs. This ensures that the template with the closest m/z value will be selected for LC peak boundary detection, interference detection and removal.
Determine the XICs of the peptide of interest at all charge states and isotope positions.
Determine the LC elution interval for the peptide of interest. To achieve this, we apply a high threshold at half maximum of the most intense (base) LC peak among all XICs. On the XIC with the tallest LC peak, all intervals above the threshold are considered as possible LC elution intervals. Then at the charge state of the base peak, we further check the correlations between the LC peaks on possible intervals at the two highest isotope positions (usually 12 C and 13 C). The interval corresponding to the peptide of interest should have a high correlation; otherwise the LC peaks must have been registered by other peptides, or have been corrupted by interference signals. The correlation is checked by R-squared statistics , and we apply a stringent threshold (> 0.9). We accept LC intervals with correlations higher than the threshold. If none of the intervals pass the threshold, we move on to the next peptide for possible template extraction. If multiple intervals have high correlations, which indicates that multiple peptides with similar mass occur on the same XIC, then we reject all intervals and move on to the next peptide since we can not detect the peptide interval unambiguously. This iterative procedure ensures that 1. We select a correct and unambiguous elution interval for the peptide of interest, and 2. The MS signal has not been corrupted by interference or noise.
If the elution interval is accepted, we determine the range of m/z values that the reference template spans (defined as the MS window of the template). The size of the MS window is determined by instrument resolution.
We average all MS peaks within the MS window and the accepted elution interval based on the MRC principle. The resulted MRC signal is an estimation of the MS peak signal registered by the peptide, and it can be used as a reference template.
After performing the above steps for each peptide, a list of reference templates has been obtained for LC peak detection. The details of XIC extraction, determination of MS windows, and the theoretical derivation of reference templates can be found in [Additional file 1].
LC peak detection
After obtaining a list of reference templates, the algorithm moves on to accurately detect and quantify the LC peak for each peptide of interest. Given a peptide, we start LC peak detection by inspecting its XICs. Usually, several LC peaks above the background noise level exist on an XIC, where, one is generated by the peptide of interest and the rest belong to others. We need to correctly identify the LC peak and its boundaries so that noise signals are not included in relative quantification. We perform the following processing steps:
Candidate LC peak generation
Given a peptide's mass (m) at a charge state (z), determine its theoretical m/z values at different isotope positions.
At the m/z value of its base peak, estimate its MS window and generate the XIC.
Apply an intensity threshold at 3 times the estimated background noise standard deviation to identify LC peak candidates.
Determine the FWHM elution intervals of LC peak candidates by applying thresholds at half maximum of these LC peak candidates. These FWHM boundaries are set as initial LC peak boundaries. In this way, we only include MS scans with relatively high SNRs.
Check the correlation between LC peaks at the most intense and the second most intense isotope positions within the initial boundaries of each LC peak candidate. The correlation is checked using R-squared statistics, and all candidates with R statistics greater than 0.9 will be accepted. In this way, all intervals with good correlations between two isotopes will be selected.
If the maximum R-statistic is less than 0.9, then the LC peak candidate with the maximum R statistics will be selected. This corresponds to the case when correlations between isotope elution profiles are poor due to noise or interference, and the peptide of interest may or may not exist. In such cases, we select the best candidate for further verification in the MS dimension.
At the end of this process, a list of k LC peak candidates, each denoted by its start and end scan, is generated at each charge state. The charge state with the highest total ion count within initial LC peak boundaries will be selected.
Next, one of these LC peak candidates will be identified as the initial LC peak.
LC peak identification
We select the closest reference template to the peptide of interest in m/z values, which ensures the best match between the template and local MS peaks. We then translate the template to the local m/z value of the peptide of interest. Details of template translation can be found in [Additional file 1].
For each LC peak candidate, estimate its local MS peak signal by averaging all MS peaks (using MRC) within its initial boundaries. By employing MRC, noise in individual MS peaks will be maximally suppressed.
The estimated local MS signal will be compared to the selected reference template. The LC peak candidate with the best matched local MS signal will be identified as the final LC peak.
If none of the local MS signals match with the reference template well (with R statistics < 0.4), then LC peak detection failed for the given peptide. This could happen when a peptide identification algorithm wrongly reports the center mass of the peptide, which leads to a mismatch between the reference template and the local MS signal. Although it is possible to correct such wrongly reported mass, however, it is beyond the scope of this paper.
At the end of this processing step, an LC peak has been identified for the peptide of interest with initial boundaries detected using a high intensity threshold at half the maximum of the LC peak.
We do not assume specific LC peak shapes (e.g. Gaussian), and the algorithm can be applied in various LC conditions (e.g., different reverse-phase gradients). If reference templates are extracted from an LC-MS experiment directly, then they will be centered at their theoretical m/z values plus the mass drift of the experiment. Thus, mass drift will be automatically accounted when applying such reference templates for LC peak detection. If a theoretical reference template is used, then its center needs to be shifted according to user provided mass calibration information.
Peptide template extraction
For a peptide of interest, its identified LC peak has an initial elution interval that covers the intensity region above half of the LC peak maximum, and it is obtained at the highest charge state and isotope position. These conditions ensure that the MRC signal associated with the identified LC peak is estimated at a high SNR, and it can be treated as the peptide template of interest. Such a template captures accurate MS peak shape information, which can be used for LC peak boundary detection and quantification.
Accurate LC peak boundary detection
The initial LC peak boundaries are obtained by applying a high intensity threshold, and many MS scans that belong to the peptide of interest are excluded. We need to accurately extend the boundaries so that all MS scans of the peptide will be accounted. If the boundaries exclude a significant segment of the LC peak, then quantification will be less accurate since combining fewer scans cannot suppress noise sufficiently. If the boundaries are extended too far to include scans that contain interference and noise, then quantification accuracy will also be reduced.
The problem of LC peak boundary detection can be translated to the problem of detecting of all scans that contain the peptide template. It can be further formulated as a hypothesis testing problem:
H0: A given MS scan only contains noise;
H1: The scan contains noise plus the peptide template.
We test the hypothesis by comparing the peptide template to the MS peak signal in a given scan. If the R-statistic is greater than a threshold (0.5), then H1 is accepted.
We start this hypothesis testing procedure from the initial LC peak starting scan to extend the head of the LC peak. Then we apply the same procedure to the tail end of the peak. Whenever encountering a scan that does not contain the template, the extension process will be terminated.
For a given peptide, we have obtained its peptide template and LC peak boundaries after LC peak detection. Based on these inputs, we can accurately quantify the peptide at other charge state and isotope positions. At a given "local m/z value" of low SNR, quantification consists of three processing steps: 1. Obtain a local MRC signal by averaging all MS peaks (using MRC) within the detected LC peak boundaries to optimally suppress noise; 2. Compare the translated peptide template with the local MRC signal for interference detection and removal. This step also provides an estimation of the scaling factor for the local MRC signal in reference to the peptide template, which can be multiplied to the total ion count of the template to derive the total ion count of the peptide at the local m/z value.
Local MRC signal are derived using weights proportional to the LC peak intensities obtained at the LC peak detection stage. The details of other processing steps are described below.
Interference detection and removal
The input to this processing step includes the local MRC signal and the translated peptide template, whose correlation is calculated using the R-square statistic . If the correlation is greater than 0.9, then it is considered that the interference signal does not exists. Otherwise, the local MRC signal is considered as interference corrupted, and we have to perform interference removal within its MS window.
We model a local MRC signal as the superposition of the translated peptide template (scaled by a) and an interference signal which is modeled as an order l polynomial. The interference removal problem is equivalent to the accurate estimation of the scale factor a and the polynomial parameters.
When assuming Gaussian noise, the Maximum Likelihood estimation of these parameters is equivalent to their least-square-estimation (LSE). Note that the correlation between the interference and the peptide template signal must be minimized to yield a good estimate of a. Otherwise, the estimated interference signal could contain partial template signal. Consequently, besides finding the LSE of parameters, the second objective is to find parameters that minimize the correlation between the template and the interference signal. In addition, there is the constraint that both the template and the interference signal should be positive at all m/z values. These requirements lead us to formulate a constrained multiple objective optimization problem. We utilize the Quadratic Programming algorithm  to numerically search for the solution of model parameters. The selection of polynomial order is based on the Bayesian Information Criteria (BIC) . See [Additional file 1] for details.
Note that there exist various peak identification algorithms [19, 20] that are specially designed to deal with the problem of overlapping peptide peaks. These algorithms are generally exponentially complex with the number of overlapping peaks considered. In this paper, the focus is on accurate quantification after peptide identification. Thus, the problem is simplified to only extract signals for the peptide of interest. The knowledge of overlapping peptides can help in improving quantification accuracy, but since peak identification algorithms may or may not provide such information, we uniformly treat overlapping signals as interference. The MRC process also has the effect of suppressing interfering signals since higher weights are given to tall MS peaks of the peptide of interest but not interfering peaks. This treatment also limits the computational complexity, which is linear to the number of peptides to be quantified.
Quantification based on local MRC signal
where w(t) are normalizing weights used for MRC. Thus if the total ion count of the peptide template is C t , the total ion count of the LC peak C p can be estimated as , where C t * a = C m is the estimated total ion count of the local MRC signal.
Data Collection and processing
We developed our algorithm based on an LC-MS dataset collected from a tryptic digest of horse myoglobin at a concentration of 600 fmol (unless noted, all illustrations in this paper are generated based on this dataset). For reference, we also obtained an LC-MS/MS dataset for peptide sequence information at 100 fmol. LC-MS/MS was performed with a splitless nanoLC-2 D pump (Eksigent), a 50 μ m-i.d. column packed with 10 cm of 5 μ m-o.d. C18 particles, and a linear ion trap tandem mass spectrometer (LTQ-XLS; ThermoFisher). The top 7 most abundant eluting ions were fragmented by (data-dependent) collision-induced dissociation (CID). The LC gradient was 2 to 98% 0.1% formic acid/acetonitrile in 60 min (60-120 min) at 400 nL/min. Tandem mass spectra were extracted by Mascot Distiller version 2.3.1. Charge-state-deconvolution and deisotoping were not performed. All MS/MS samples were analyzed using Mascot (Matrix Science, London, UK; version 2.3.2). Mascot was set up to search the Swiss-Prot database assuming the digestion enzyme trypsin. Mascot was searched with a fragment ion mass tolerance of 0.80 Da and a parent ion tolerance of 2.0 Da. Oxidation of methionine and iodoacetamide derivative of cysteine were specified in Mascot as variable modifications. LC-MS was performed with a splitless nanoLC-2 D pump (Eksigent), a 50 μ m-i.d. column packed with 10 cm of 5 micro-o.d. C18 particles, and a time-of-flight mass spectrometer (MicrOTOF; Bruker Daltonics). The LC gradient was 2 to 98% 0.1%formic acid/acetonitrile in 60 min (60-120 min) at 400 nL/min. Mascot search correctly linked 13 peptides observed in the sample to horse myoglobin with an 80% sequence coverage.
For algorithm verification, we downloaded a QTOF dataset from the repository of Seattle Proteome Center at http://regis-web.systemsbiology.net/PublicDatasets/. The repository was created for testing various algorithms. It contains LC-MS/MS datasets of an 18 protein digest. For details of data collection please refer to . There are multiple LC-MS/MS datasets collected on various instruments within the repository. We downloaded datasets related to protein mixture 4 of the 18 protein mix. Among which, from a total of 21 runs on LTQ-FT, QStar and QTOF, we compiled a list of 784 LC-MS/MS-identified peptides for the same protein mixture. These peptides were all identified with a PeptideProphet™ score greater than 0:9. We also performed LC-MS peak detection using msInspect on one of the QTOF datasets QT 20060925_mix 4_23.mzxml (mix4_23) that identified 1952 peptides. Subsequently we quantify these peptides by MRCQuant. MsInspect was selected because it is the most representative LC-MS peptide identification and quantification algorithm and has been shown to outperform other peak detection algorithms . It applies a conservative noise threshold initially. Subsequently, MS scans are centroided; XICs are smoothed; LC peak length filter is applied; and LC peaks that appear and disappear together are pooled and treated as signals registered by identical peptides at different isotope positions and charge states. Subsequently, peptides are identified by comparing their theoretically predicted isotope patterns and measured isotope patterns using Kullback-Leibler(KL) distance. Other popular software packages such as ASAPRatio  differ slightly in the details, but the main procedure, MS peak detection in each MS scan followed by quantification based on XICs, is similar to that of msInspect. Among these software packages, msInspect provides relative quantification accuracy measurements in the form of KL distance, which enables us to compare performances. Other software packages do not provide this measurements, therefore, relative quantification accuracy cannot be accessed.
When using the msInspect software package (Build 599) to process mix 4_23 dataset, we tried to optimize the number of peptides being reported. We selected the "walksmooth" option when running the command "findPeptides", and we set msInspect parameters "minpeaks" to 2 and "maxkl" to 10. The "walksmooth" option greatly improves the number of features as well as the KL scores reported. A total of 1952 features were reported. In comparison, if the default settings of msInspect are used, 933 features were reported with worse KL scores.
The peptides reported by msInspect were further processed by MRCQuant. We used extracted templates at high SNRs as reference MS templates. We rejected some msInspect reported features either because: their reported msInspect KL scores are negative, or our algorithm determines that the LC peaks reported by msInspect cannot be found. The latter case could be caused by inaccurate mass reporting by msInspect. When the mass is reported inaccurately, the reference template and the local MS signal would deviate from each other significantly, and our algorithm rejects LC peaks when the R statistic between the reference template and the local MS signal is less than 0.4. Correcting the incorrectly reported mass is a peptide identification problem which is beyond the scope of this paper. This results in a peptide list of length 964 with accurately reported mass values.
Relative quantification accuracy evaluation
If two sets of isotope ratios entirely agree with one another, then their KL score equals to zero. Otherwise, a KL score is always positive, and the larger it is, the bigger the difference between the two sets of isotope ratios.
Different KL scores indicate different levels of quantification accuracy, and it is possible to compare the performance of different algorithms by the reported number of peptides at different KL score thresholds. For example, we can claim that algorithm one is better than algorithm two, if algorithm one reports more peptides with KL scores less than a threshold.
Obviously, we cannot set the KL threshold to infinity, and now the question becomes what could constitute an "acceptable range of KL thresholds". We know that given a KL score, there always exist the probability that it is the divergence between an arbitrarily generated and an authentic isotope distribution. The higher the KL score is, the higher the probability. If the KL score of a reported peptide is high, it is very probable that the real peptide signal does not exist, and the reported isotope distribution is generated based on observations of random noise. This probability is defined as the False-Detection-Rate (FDR), which can be converted from a KL score in reference to a KL null distribution (the distribution of KL scores between authentic peptide and arbitrarily generated isotope ratios). Obviously, when the FDR is high, it is not meaningful to compare the reported number of peptides between two algorithms anymore, since a significant portion of reported peptides should have been falsely detected. In this paper, we adopt a cutoff FDR of 12%, and we compare the number of reported peptides at different FDRs less than 0.12.
Given a KL score reported by an algorithm, to convert it to FDR, the p-value of the KL score is first generated based on the KL null distribution. Subsequently, the FDR is estimated using the method described in  based on the p-value. The Matlab function, mafdr(·), is used to estimate the FDRs from the p-values.
The null distribution on KL score is generated by calculating the KL scores between arbitrarily generated isotope distributions with authentic ones. Without observations, an arbitrary distribution on isotopes is generated by drawing maxiso random numbers uniformly distributed on 0, and then these numbers are normalized to form a distribution. We generate authentic theoretical isotope distributions by randomly drawing mass values from the peptide list reported by msInspect, and then for these mass values, we calculate their theoretical isotope ratios using the method in .
Results and Discussion
Performance comparison between MRCQuant and msInspect
We also compared the performance of msInspect and MRCQuant based on LC-MS/MS-identified peptides. However, when allowing a 10 ppm tolerance, there are only 31 LC-MS/MS-identified peptides that overlap with msInspect-reported peptides. In other words, most peptides compiled from multiple LC-MS/MS runs were not reported by msInspect. With such a small number of overlaps, we could not perform a meaningful comparison. In contrast to the low detection rate of LC-MS/MS-identified peptides by msInspect, MRCQuant quantified 423 LC-MS/MS-identified peptides in total, among which, 203 have an FDR <= 0.1.
Performance at different intensity levels
Effect of using different templates
In this paper, we describe a new algorithm called "MRCQuant" for LC-MS relative quantification of "bottom-up" proteomics data based on extracted MS templates. Reference- and peptide- MS templates are extracted from scans with relatively high SNRs using MRC, a process that optimally suppresses noise.
Subsequently, these templates are used for detecting LC peak boundaries, detecting interference, and removing noise at lower SNRs. MRCQuant performs automatic mass drift correction by utilizing extracted MS templates which capture mass deviation from theoretical mass values. These techniques address major deficiencies in previous LC-MS quantification algorithms effectively. We demonstrate significant improvement in relative quantification accuracy with a larger number of detected peptides at low FDRs compared to msInspect. We expect that MRCQuant can be integrated with various LC-MS processing software to improve the overall performance. For example, MRCQuant can be readily modified and applied in label and label-free proteomic experiments for quantitative analysis. The proposed algorithm can also be incorporated in LC-MS peak detection algorithms that use isotope ratios.
Availability and requirements
Relevant data and source Matlab scripts are available at project home page:http://compgenomics.utsa.edu/MRCquant.html
This work is supported by San Antonio Life Sciences Institute Research Enhancement, and a grant from National Institute of Health (NIH 2G12RR013646-11). The authors thank the RCMI Proteomics and Protein Biomarkers Cores at UTSA for assistance with experiment design, sample preparation, data collection, results interpretation, and manuscript preparation. We thank the Computational Biology Initiative (UTSA/UTHSCSA) for providing access and training to the analysis software used. Lastly, the authors gratefully acknowledge the support of the Cancer Therapy and Research Center (CTRC) at the University of Texas Health Science Center San Antonio, an NCI-designated Cancer Center. (NIH P30CA54174). This work is also partially supported by grants from the Virginia G. Piper Charitable Trust and the Flinn Foundation of Arizona.
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