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Citation for this paper:

Abbatiello, S., Ackermann, B. L., Borchers, C., Bradshaw, R. A., Carr, S. A., Chalkley, R., … Zimmerman, L. (2017). New Guidelines for Publication of Manuscripts Describing

Development and Application of Targeted Mass Spectrometry Measurements of Peptides and Proteins. Molecular & Cellular Proteomics, 16(3), 327-328.

https://doi.org/10.1074/mcp.E117.067801.

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New Guidelines for Publication of Manuscripts Describing Development and

Application of Targeted Mass Spectrometry Measurements of Peptides and Proteins

Susan Abbatiello, Bradley L. Ackermann, Christoph Borchers, Ralph A. Bradshaw,

Steven A. Carr, Robert Chalkley, … Lisa Zimmerman

March 2017

© 2017 Susan Abbatiello et al. This is an open access article distributed under the terms of the Creative Commons Attribution License. https://creativecommons.org/licenses/by-nc-nd/4.0/

This article was originally published at:

https://doi.org/10.1074/mcp.E117.067801

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New Guidelines for Publication of Manuscripts

Describing Development and Application of

Targeted Mass Spectrometry Measurements of

Peptides and Proteins

Susan Abbatiello‡§, Bradley L. Ackermann¶, Christoph Borchers

储,

Ralph A. Bradshaw**, Steven A. Carr‡

e

, Robert Chalkley§§, Meena Choi¶¶,

Eric Deutsch

储储, Bruno Domon

a

, Andrew N. Hoofnagle

b

, Hasmik Keshishian‡,

Eric Kuhn‡, Daniel C. Liebler

c

, Michael MacCoss

b

, Brendan MacLean

b

, DR Mani‡,

Hendrik Neubert

d

, Derek Smith

储, Olga Vitek¶¶, and Lisa Zimmerman

c

Molecular & Cellular Proteomics is pleased to announce new guidelines and requirements for papers describing the development and application of targetedmass spectrometry measurements of peptides, modified peptides and proteins

(PDF). These guidelines will be implemented for papers sub-mitted starting June, 2017.

Over the past several years, representatives from aca-demia, clinical laboratories, and pharma, who are active de-velopers and users of targeted mass spectrometry methods and analysis tools for quantification of peptides and proteins in complex biological or clinical samples, have worked to-gether to develop a set of guidelines and requirements for

authors who want to publish targeted proteomics papers. Our goals were to define what information authors must provide regarding how such analyses were performed and the result-ing data analyzed to ensure that reviewers and readers have the ability to independently establish that the measurements being reported using targeted MS methods are reliable—i.e. that they specifically identify and quantify the analytes tar-geted in a sample—and that the measurements are reproduc-ible. The guidelines and requirements for authors that have been developed grew out of an NCI-sponsored meeting and subsequent publication describing a tiered, fit-for-purpose approach to targeted assay development in mass spec-trometry-based proteomics (1). We have also incorporated numerous helpful and important suggestions from the com-munity obtained during the 4-month-long public commen-tary period.

The need for establishing guidelines for targeted MS meas-urements parallels the situation in discovery proteomics prior to 2004 when similar issues relating to lack of ability to as-certain reliability of published results prompted the journal Molecular & Cellular Proteomics to develop and adopt the first set of guidelines for publication of peptide and protein iden-tification data using mass spectrometry (2). These guidelines, which have been repeatedly revised and updated over the past several years (3–5), have been embraced in whole or in part by other journals. The goal now, as it was then, is to try

From the ‡Broad Institute of MIT and Harvard, Cambridge, Mas-sachusetts; ¶Eli Lilly, Indianapolis, IN;储University of Victoria, Vic-toria, British Colombia; **University of California, Irvine, California; §§University of California, San Francisco, California; ¶¶Northeast-ern University, Boston, Massachusetts;储储Institute for Systems Bi-ology, Seattle, Washington;aLuxembourg Clinical Proteomics

Cen-ter, Luxembourg;bUniversity of Washington, Seattle, Washington; cVanderbilt University, Nashville, Tennessee; dPfizer, Andover,

Massachusetts

Received February 9 2017

Published, February 9, 2017, MCP Papers in Press, DOI 10.1074/ mcp.E117.067801

Author contributions: S.E.A., B.L.A., C.H.B., R.A.B., S.A.C., R.J.C., M.C., E.W.D., B.D., A.N.H., H.K., E.K., D.C.L., M.J.M., B.M., D.M., H.N., D.S., O.V., and L.Z. wrote the paper.

REFERENCES

1. Carr, S. A., et al. (2014) Targeted peptide measurements in biology and medicine: Best practices for mass spectrometry-based assay devel-opment using a fit-for-purpose approach. Mol. Cell. Proteomics 13, 907–917

2. Carr, S. A., Aebersold, R., Baldwin, M., Burlingame, A., Clauser, K., and Nesvizhski A. (2004) The need for guidelines in publication of

peptide and protein identification data. Mol. Cell. Proteomics 3, 531–533

3. Bradshaw, R. A., Burlingame, A. L., and Carr S. A. (2005) Revised draft guidelines for proteomic data publication. Mol. Cell. Proteomic 4, 1223–1225

4. Chalkley, R. J., Clauser, K. R., and Carr, S. A. (2009) Updating the MCP proteomic publication guidelines. ASBMB Today 16 –17

5.http://www.mcponline.org/site/misc/ms_guidelines.xhtml

Editorial

© 2017 by The American Society for Biochemistry and Molecular Biology, Inc. This paper is available on line at http://www.mcponline.org

crossmark

Molecular & Cellular Proteomics 16.3

327

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to ensure that reliable and reproducible high quality data and results are entering the proteomics literature. We have endeavored to avoid making these guidelines overly pre-scriptive and intend to be flexible so as to allow for new technologies and approaches that will inevitably arise. We also intend to regularly revisit and revise the guidelines as

needed, as we have done for our other documents for author guidance.

eTo whom correspondence should be addressed: Proteomics, The

Broad Institute of MIT and Harvard, 415 Main St., Cambridge, MA 02142. Tel.: 617-714 7630; E-mail: scarr@broad.mit.edu.

§ Currently at Thermo Scientific, Cambridge, MA.

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