Hi everyone, the iPRG 2012 study has been announced. Your participation in
the study is encouraged.





[image: cid:[email protected]]
Association of Biomolecular Resource Facilities
*Business Office:
*9650 Rockville Pike, Bethesda, MD  20814
Tel: 301-634-7306     Fax: 301-634-7455     Email: [email protected]



*Re: iPRG-2012: Proteome Informatics Research Group Study:*

*Detecting modified peptides in a complex mixture*



Dear Potential Study Participant,

Nature uses a wide variety of protein post-translational modifications to
regulate protein structure and activity and tandem mass spectrometry has
emerged as the most powerful analytical approach to detect these moieties.
However, modified peptides present special challenges for
characterization.  First, they are generally present at sub-stoichiometric
levels, meaning that without enrichment strategies samples are dominated by
unmodified peptides, so finding the modified peptides may be a challenge.
Secondly, the modifications may have unique fragmentation behaviors in
collision-induced dissociation (CID), which may need to be considered by
database search engines.  Finally, if there are multiple residues within a
given peptide that could bear a particular modification type, then it is
necessary to identify fragment ions that frame either side of the
modification site in order to be able to localize the exact site of
modification within the peptide.

The Proteome Informatics Research Group (iPRG) of the Association of
Biomolecular Resource Facilities (ABRF) invites you to participate in a
collaborative data analysis study to enable proteomics laboratories to
evaluate their ability to find a variety of post-translationally modified
peptides within a complex peptide mixture background. The dataset consists
of nearly twenty thousand high resolution and high mass accuracy tandem
mass spectra. Within the sample there are peptides with a range of
different natural and chemical modifications. This study will enable
participants to evaluate their data analysis capabilities and approaches
relative to others in analyzing a common data set, with a particular
emphasis on their ability to detect and characterize peptides with
modifications of potential biological significance..

Participants will be supplied with data in a range of formats and a
template for reporting results.  Upon completion, the participant will also
be asked to complete a web-based questionnaire summarizing the methods they
used.  Results submission is anonymous, so whether you are experienced in
this type of analysis or not, we encourage you to take part.

This study will be launched on January 5th 2012 and results must be
returned by February 3rd 2012 in order to enable sufficient time to analyze
the results for presentation at the 2012 ABRF Meeting (March 17th-20th 2012
in Orlando, FL). If you would like to take part or get more information,
please download the study participation instructions from the ABRF iPRG web
site:
http://www.abrf.org/index.cfm/group.show/ProteomicsInformaticsResearchGroup.53.htm

This study is open to both ABRF members and non-members. However, we do
strongly encourage non-members to join, and thus help support ABRF (for
more information visit http://www.abrf.org). A summary of the results of
this study will be presented orally and as a poster at the ABRF 2012
meeting, subsequently posted on the ABRF website, and published in a peer
reviewed journal.

We thank you for your support of the ABRF and look forward to your
participation in this year's study.



Sincerely,

* *

*The ABRF Proteome Informatics Research Group (iPRG)*

Robert Chalkley – UCSF (Chair)

Nuno Bandeira - UCSD

Matt Chambers – Vanderbilt University

Karl Clauser - Broad Institute of MIT and Harvard

John Cottrell – Matrix Science Ltd

Eric Deutsch - Institute for Systems Biology

Eugene A. Kapp - WEHI

Henry Lam - Hong Kong University of Science and Technology

W. Hayes McDonald - Vanderbilt University

Ruixang Sun – Chinese Academy of Sciences

Thomas Neubert (EB Liaison) - New York University

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