The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index; 5 of the 34 sources its claims cite were checked for support.
A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards
Open accessAbstract
Absolute protein quantification using mass spectrometry (MS)-based proteomics delivers protein concentrations or copy numbers per cell. Existing methodologies typically require a combination of isotope-labeled spike-in references, cell counting, and protein concentration measurements. Here we present a novel method that delivers similar quantitative results directly from deep eukaryotic proteome datasets without any additional experimental steps. We show that the MS signal of histones can be used as a "proteomic ruler" because it is proportional to the amount of DNA in the sample, which in turn depends on the number of cells. As a result, our proteomic ruler approach adds an absolute scale to the MS readout and allows estimation of the copy numbers of individual proteins per cell. We compare our protein quantifications with values derived via the use of stable isotope labeling by amino acids in cell culture and protein epitope signature tags in a method that combines spike-in protein fragment standards with precise isotope label quantification. The proteomic ruler approach yields quantitative readouts that are in remarkably good agreement with results from the precision method. We attribute this surprising result to the fact that the proteomic ruler approach omits error-prone steps such as cell counting or protein concentration measurements. The proteomic ruler approach is readily applicable to any deep eukaryotic proteome dataset-even in retrospective analysis-and we demonstrate its usefulness with a series of mouse organ proteomes.
Overview
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Written from the paper’s full text.
TL;DR
The paper introduces a label-free “proteomic ruler” that uses histone MS signal as a proxy for DNA amount to estimate total protein per cell and protein copy numbers without spike-in standards or cell counting. It reports agreement with spike-in/SILAC and biochemical estimates across cell lines, plasma, and mouse tissues.
Key findings
- In four human cell lines, histone peptides accounted for 2.07–4.03% of total MS signal; equating that to 6.5 pg DNA per diploid cell gave protein mass per cell within 1.24 ± 0.29-fold of cell-counting values.
- Ribosomal protein signal was 3.61–5.27% of total MS signal, and RNA estimates from this signal were within 1.01 ± 0.13-fold of biochemical RNA measurements.
- Reanalysis of a PrEST-SILAC dataset gave copy numbers deviating on average 1.5-fold from spike-in values; label-free estimates used 19.4 peptides per protein on average versus 4.7 for PrEST-SILAC, and larger deviations occurred when PrEST-SILAC used ≤2 peptides or label-free used ≤11 peptides.
- In mouse organs, ovary cells had 42 pg protein per cell and leg muscle about 675 pg per nucleus; liver averaged 464 ± 35 pg per cell, thymus 59 ± 31 pg, and dendritic cell subtypes 64 ± 14 to 95 ± 25 pg.
Methods
- Samples included human plasma, four cultured human cell lines (U87-MG, A549, PC-3, Hep-G2), and mouse tissues; proteins were processed by FASP with LysC/trypsin digestion, and DNA/RNA were released by RNase/DNase and measured by A260.
- LC-MS/MS used Q Exactive with HCD or LTQ Orbitrap with CID; data analyzed in MaxQuant/Andromeda against human and mouse UniProt proteomes, with 1% FDR and a Perseus plugin for absolute abundance calculations.
- Absolute scaling used the Total Protein Approach and histone proteomic ruler; comparisons were made with cell counting, DNA-based cell number estimates, biochemical RNA/protein measurements, PrEST-SILAC copy numbers, and retrospective dendritic cell proteome data.
Limitations
- The authors state the method requires eukaryotic whole-cell proteome data with unbiased chromatin representation and sufficient depth; histone fraction stabilized only from about 12,000 peptides onward. They also note that in syncytial muscle the ruler yields protein per nucleus rather than per cell.
- The authors acknowledge assumptions that allow omission of spike-ins, and they report typical agreement within about a factor of 2 with precision measurements or literature values.
- Evident from the text: validation is limited to a small set of cell lines, plasma, and selected mouse tissues; accuracy depends on known genome size/ploidy and on the assumed DNA-to-histone mass relationship; the retrospective dendritic cell dataset came from in-gel digestion, which the paper notes is incompatible with direct DNA quantification.
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Claims the paper makes
27 Own interpretation · 27 Own result · 25 Not checked yet · 10 No basis given · 1 Supported so far · 1 Partly supported · 1 Own method · accuracy not yet measured
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In the paper
“Existing methodologies typically require a combination of isotope-labeled spike-in references, cell counting, and protein concentration measurements.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > Abstract
What the sources say
- Partly supportedcites [9] Schwanhausser, 2011, Global quantification of mammalian gene expression control, Nature sourceExperimental — accuracy not yet measured
The Reproducibility section (p. 8) reports spike-in experiments to validate absolute protein quantification. It does not say those spike-ins were isotope-labeled or generally required, and the cited passages do not establish a requirement for cell counting or protein concentration assays. (LLM, conf=0.78)
- Partly supportedcites [10] Beck, 2011, The quantitative proteome of a human cell line, Mol. Syst. Biol sourceExperimental — accuracy not yet measured
The Results describe heavy-isotope-labeled reference peptides spiked into extracts from a specified number of U2OS cells, supporting the spike-in and cell-count elements for this study. The Materials and methods section also describes spiking AQUA peptides, but the passages do not establish that protein concentration assays were required or that existing workflows typically require all three measurements. (LLM, conf=0.84)
- Partly supportedcites [11] Zeiler, 2012, A protein epitope signature tag (PrEST) library allows SILAC-based absolute quantification and multiplexed determination of protein copy numbers in cell lines, Mol. Cell. Proteomics sourceExperimental — accuracy not yet measured
The Abstract describes established absolute-quantification methods using labeled spike-in standards, and the Results and Experimental Procedures describe measuring a standard’s protein concentration and counting cells to calculate HeLa protein copy numbers (page not provided). Cell counting is supported for copy-number determination, but the paper does not establish it as a typical requirement of absolute protein quantification workflows generally. (LLM, conf=0.86)
plain- Asserted: passes — The authors put it forward as true.
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- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“which in turn depends on the number of cells.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > Abstract
What the sources say
- Not checked yetcites [23] Papadimitriou, 1993, Measurement of cell numbers in microtiter culture plates using the fluorescent dye Hoechst 33258, J. Immunol. Methods source
- Supportedcites [24] Shimada, 2010, Normalization using ploidy and genomic DNA copy number allows absolute quantification of transcripts, proteins and metabolites in cells, Plant Methods source
In Results and Discussion, Table 1 expresses genomic DNA copy number per sample volume and genome copy number per cell, supporting the relationship between sample DNA and cell number. The paper also accounts for ploidy, which affects DNA copy number per cell. (LLM, conf=0.85)
- Supportedcites [25] Silva, 2013, Measurement of DNA concentration as a normalization strategy for metabolomic data from adherent cell lines, Anal. Chem source
In Results and Discussion (“DNA concentration is a robust surrogate for cell number”), DNA concentration had a strong linear relationship with seeded cell number (R² = 0.98), supporting the claim that DNA amount depends on cell number. The Conclusions note that ploidy, nuclei per cell, and cell-cycle effects can alter the DNA-to-cell-number ratio. (LLM, conf=0.92)
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In the paper
“we demonstrate its usefulness with a series of mouse organ proteomes.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > Abstract
boosted- Asserted: passes — The authors put it forward as true.
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In the paper
“The proteomic ruler approach yields quantitative readouts that are in remarkably good agreement with results from the precision method.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > Abstract
boostedcorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“We were able to quantify proteins within their expected physiological ranges over at least 5 orders of magnitude (Fig. 1, supplemental Table S1).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
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In the paper
“the fraction of the cumulative histone to total MS signal changed only by 5% to 10% (Fig. 4D).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
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“Dividing the total amount of protein input by these cell numbers, we obtained a protein mass per cell that was very similar to that obtained by dividing the total protein input amount by the counted cell numbers (supplemental Table S2).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
plainn = 4- Asserted: passes — The authors put it forward as true.
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- Rests on an assumption: The analyzed cell lines have diploid genomes, so their DNA mass per cell is 6.5 pg.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Within the first few thousand peptides, the histone fraction is overestimated because histones contribute some of the most intense peptides.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“From a depth of around 12,000 or more peptides, however, the histone fraction stabilizes within tight margins.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
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“Our results were within a factor of 1.01 ± 0.13 of the biochemical measurements”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
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In the paper
“Yields were greater than 95% and were independent of the protein content (Fig. 2B)”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
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In the paper
“In triplicate analyses, MaxQuant identified about 7000 proteins in each of the cell lines (supplemental Table S1).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
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In the paper
“Interestingly, our observed similarities in cell sizes correlate with overall patterns of proteomic similarity on the level of individual proteins that were observed in the original study (36).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
What the sources say
- Not checked yetcites [36] Luber, 2010, Quantitative proteomics reveals subset-specific viral recognition in dendritic cells, Immunity source
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In the paper
“Independent of the tissue of origin, low-abundant proteins had an average molecular mass of around 100 kDa, and this value decreased with increasing cellular abundance of the proteins to around 40 kDa for the most abundant proteins.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
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In the paper
“Notably, in skeletal muscle cells, filaments and motorproteins such as titin and myosins are notable exceptions to the trend of abundant proteins being smaller, as they are both large (>150 kDa) and very abundant (>1 million copies per cell) in this tissue, resulting in a profound increase in the average molecular protein mass in a muscle cell (Fig. 6C, circles).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
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In the paper
“Ovaries consist predominantly of small follicular cells and showed the least protein per cell (42 pg).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
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In the paper
“Here we present a novel method that delivers similar quantitative results directly from deep eukaryotic proteome datasets without any additional experimental steps.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > Abstract
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In the paper
“DNA concentration was shown to be proportional to the cell count and was successfully used to normalize enzyme activities, transcript and protein amounts, and metabolome data (23–25).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
What the sources say
- Not checked yetcites [23] Papadimitriou, 1993, Measurement of cell numbers in microtiter culture plates using the fluorescent dye Hoechst 33258, J. Immunol. Methods source
- Not checked yetcites [24] Shimada, 2010, Normalization using ploidy and genomic DNA copy number allows absolute quantification of transcripts, proteins and metabolites in cells, Plant Methods source
- Not checked yetcites [25] Silva, 2013, Measurement of DNA concentration as a normalization strategy for metabolomic data from adherent cell lines, Anal. Chem source
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In the paper
“However, cells are not necessarily uniform; therefore scaling by cell numbers may be inaccurate, as a 25% variation of the diameter of a sphere-shaped cell corresponds to a 2-fold change in cell volume.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > Abstract
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In the paper
“The total protein concentration in plasma varies around a typical value of 70 g/l within a narrow margin (22)”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
What the sources say
- Not checked yetcites [22] Kratz, 2004, Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Laboratory reference values, N. Engl. J. Med source
plain- Asserted: passes — The authors put it forward as true.
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In the paper
“As a result, our proteomic ruler approach adds an absolute scale to the MS readout and allows estimation of the copy numbers of individual proteins per cell.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > Abstract
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In the paper
“We termed the method the Total Protein Approach, because we relate this proportion to a total protein mass. To obtain copy numbers, we specifically used the total protein mass per cell, which needs to be determined or estimated separately.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > Abstract
What the sources say
- Not checked yetcites [16] Wisniewski, 2012, Extensive quantitative remodeling of the proteome between normal colon tissue and adenocarcinoma, Mol. Syst. Biol source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“In tissues, not only are cell sizes variable, but visual counting of cells is also problematic. For instance, up to 5-fold differences in calculated cell volumes have been reported for enterocytes of the intestinal mucosa (15).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > Abstract
What the sources say
- Not checked yetcites [15] Crowe, 1993, Morphometric analysis of small intestinal mucosa. IV. Determining cell volumes, Virchows Archive A Pathol. Anat. Histopathol source
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In the paper
“In contrast to in-solution or in-gel approaches, the FASP method is reactor based (26) and allows sequential processing of the sample and separation of reaction products.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
What the sources say
- Not checked yetcites [26] Zhou, 2011, Proteomic reactors and their applications in biology, FEBS J source
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In the paper
“The human genome contains around 3.2 × 109 base pairs (28).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
What the sources say
- Not checked yetcites [28] 2004, Finishing the euchromatic sequence of the human genome, Nature source
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In the paper
“This indicates that, with the exception of histone H3, the fraction of the MS signal derived from histone peptides that have PTMs is low and can be neglected in the overall data scaling process.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
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In the paper
“In eukaryotic cells, DNA is packaged in chromatin by histones, and the mass of the DNA is about equal to the combined mass of histones (29).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
What the sources say
- Not checked yetcites [29] van Holde, 1989
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“This depth of analysis is easily attainable with minimal sample fractionation and also with single run analyses on latest-generation machines (30).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
What the sources say
- Not checked yetcites [30] Nagaraj, 2012, System-wide perturbation analysis with nearly complete coverage of the yeast proteome by single-shot ultra HPLC runs on a bench top Orbitrap, Mol. Cell. Proteomics source
plain- Asserted: passes — The authors put it forward as true.
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In the paper
“which is reasonable given that non-hepatocytes contribute the same amount of DNA or histones but less overall protein mass.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
plain- Asserted: passes — The authors put it forward as true.
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In the paper
“which is expected to be slightly smaller than observed cell sizes, given the numerous dendrites projecting from the cell surfaces.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
plainconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“This observation underlines the benefits of approaches that rely on multiple independent quantifications instead of single peptide ratios”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
plaincorrelational- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. It may be too vague to check against evidence.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“We conclude that for those proteins quantified with more than a few peptides, the proteomic ruler approach could offer a surprisingly high level of accuracy, making it an attractive alternative to label-based methods.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
hedgedconditional- Asserted: passes — The authors put it forward as true.
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A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Using the MS signal derived from histones and relating it to a known amount of DNA per cell provides accurate estimates of the total protein amount per cell that can be used as scaling factors for calculating cellular copy numbers of any protein of interest.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > DISCUSSION
plaindirect- Asserted: passes — The authors put it forward as true.
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- The authors state this as an assumption: A protein's cumulative mass in the proteomic sample is directly proportional to the MS signals summed over all peptides derived from it.
In the paper
“Perseus is part of the freely available MaxQuant suite (20).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
What the sources say
- Not checked yetcites [20] Cox, 2008, MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification, Nat. Biotechnol source
plain- Asserted: passes — The authors put it forward as true.
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In the paper
“This dependence was observed in earlier studies and is thought to reflect the evolutionary advantage of decreasing the size of abundant proteins for reasons of biosynthetic cost (38).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
What the sources say
- Not checked yetcites [38] Warringer, 2006, Evolutionary constraints on yeast protein size, BMC Evolutionary Biol source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Importantly, this information comes for free, in that it incorporates absolute quantification into any kind of in-depth proteome dataset, even in retrospective analysis.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > DISCUSSION
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“proteins having a high fraction of theoretical peptides per sequence length and a high number of actually identified peptides, most of which are group-unique, are expected to yield better quantification.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: fails — The paper may give no reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds.
The paper relies on this without support.
Protein determination reagents can cross-react with non-protein cell components such as thiols, nucleic acids, and phospholipids.
“An additional, often ignored source of errors is the cross-reactivity of the reagents with non-proteinaceous cell components such as thiols, nucleic acids, and phospholipids.”
The paper relies on this without support.
The summed MS signal from all histone-derived peptides is proportional to cumulative histone mass.
“This value reflects the cumulative histone mass.”
The paper relies on this without support.
The analyzed cell lines have diploid genomes, so their DNA mass per cell is 6.5 pg.
“We used a value of 6.5 pg for a diploid human cell to calculate cell numbers.”
The authors state this as an assumption.
A protein's cumulative mass in the proteomic sample is directly proportional to the MS signals summed over all peptides derived from it.
“our copy number calculation assumes a direct proportionality between a protein's cumulative mass in the proteomic sample and the MS signals summed over all peptides derived from it (see Eq. 3).”
The paper relies on this without support.
Many obligate protein complexes are well characterized in terms of composition and stoichiometry, with subunits expressed at equimolar levels.
“Many obligate protein complexes are well characterized in terms of their composition and stoichiometry with subunits expressed at equimolar levels.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Also, DNA and histones are good proxies for each other as the number of histones per cell is proportional toward amount of DNA per cell, that is, same for all 2N human cells (Wiśniewski et al, 2014) (note: not applicable for cell lines with different karyotypes)”
From Gene‐specific correlation of RNA and protein levels in human cells and tissues (2016) · cites this paper as Wiśniewski et al, 2014
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
“Fig. 5C shows that our histone proteomic-ruler-derived copy numbers of members of the pyruvate dehydrogenase complex and the TRiC chaperone closely match the expected 1:1 stoichiometry among subunits.”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
“C, pyruvate dehydrogenase complex. D, TRiC chaperonin.”
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
“we ranked all peptides by intensity and calculated the histone-MS fraction as a function of the number of identified peptides (Fig. 4E).”
§ A “Proteomic Ruler” for Protein Copy Number and Concentration Estimation without Spike-in Standards* > RESULTS
“D, histone MS signal fraction as a function of the depth of analysis, simulated by intensity-based ranking of peptides.”
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Metadata
- Authors
- Wiśniewski, J. R., Hein, M. Y., Cox, J., & Mann, M.
- Affiliations
- Max Planck Institute of Biochemistry (DE)
- Corresponding author
- Wiśniewski, Jacek R.
- Mann, Matthias
- Venue
- Molecular & Cellular Proteomics
- Publisher
- Elsevier BV
- Published
- 2014-12
- Volume
- 13
- Issue
- 12
- Pages
- 3497-3506
- ISSN
- 1535-9476 (ISSN-L)
- PMC
- PMC4256500
- OpenAlex
- W2152983548
- Cited by
- 690
- References
- 44
- Citations by year
- 2026: 58 · 2025: 77 · 2024: 82 · 2023: 67 · 2022: 69 · 2021: 57 · 2020: 73 · 2019: 40 · 2018: 62 · 2017: 39 · 2016: 35 · 2015: 25 · 2014: 5
- FWCI
- 14.86
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Molecular & Cellular Proteomics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Max Planck Digital Library (submittedVersion, other-oa)
- MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
- Funders
- European Commission (201648)
- Max-Planck-Gesellschaft
- Topics
- Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
- Physical Sciences › Chemistry › Spectroscopy › Mass Spectrometry Techniques and Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Advanced Biosensing Techniques and Applications
- Keywords
- absolute protein quantification, histones, DNA content
- MeSH terms
- Amino Acids, Animals, Cell Count, DNA, Histones, Humans, Isotope Labeling, Reference Standards, Gene Expression, Proteome, Cell Line, Tumor, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
A language model drew the claims from the paper on 2026-10-05, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-05 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
Cited sources are checked with a language model’s help (gpt-6-sol).
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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