<<< Full experiment listing

PXD048271-1

PXD048271 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleWideband PRM: Highly Accurate and Sensitive Method for High-Throughput Targeted Proteomics
DescriptionTargeted mass spectrometry (MS) approaches, which are powerful methods for uniquely and confidently quantifying a specific panel of proteins in complex biological samples, play a crucial role in validation and clinical translation of protein biomarkers discovered by global proteomic profiling. Common targeted MS methods, such as multiple reaction monitoring (MRM) and parallel-reaction monitoring (PRM), employ specific mass spectrometric technologies to quantify protein levels by comparing the transitions of specific endogenous (Endo) peptides with those of stable isotope labeled (SIL) peptide counterparts. These methods utilizing amino acid analyzed (AAA) SIL peptides warrants sensitive and precise measurements required for targeted MS assays. Compared to MRM, PRM provides higher experimental throughput by simultaneously acquiring all transitions of the target peptides and thereby compensate for different ion suppression among transitions of a target peptide. However, PRM still suffers different ion suppressions between Endo and SIL peptides due to poor spray stability as the Endo and SIL peptides were monitored at different liquid chromatography (LC) retention times. Here we introduce a new targeted MS method, termed as wideband PRM (WBPRM), designed for high-throughput targeted MS approach. WBPRM employs a wide isolation window for simultaneous fragmentations of both Endo and SIL peptides along with multiplexed single ion monitoring (SIM) scans for enhanced MS sensitivity of target peptides. Compared to PRM, WBPRM was demonstrated to provide increased sensitivity, precision, and accuracy of quantitative measurements of target peptides with increased throughput, allowing more target peptide measurements in a short experiment time. Its adaptability to a MS method provided by the manufacture makes it a facile method to implement for MS based assays, particularly in complex biological samples, where the needs for higher accuracy, sensitivity and efficiency are paramount.
HostingRepositoryPRIDE
AnnounceDate2024-08-14
AnnouncementXMLSubmission_2024-08-14_10:21:34.093.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterDowoon Nam
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListphosphorylated residue; 6x(13)C labeled residue; iodoacetamide derivatized residue
InstrumentOrbitrap Exploris 480
Dataset History
RevisionDatetimeStatusChangeLog Entry
02024-01-05 01:46:27ID requested
12024-08-14 10:21:34announced
22024-10-22 06:54:58announced2024-10-22: Updated project metadata.
Publication List
10.1021/acs.analchem.4c00518;
Nam D, Ji M, Kang C, Kim H, Yang H, Bok KH, Bae J, Hong J, Lee SW, Wideband PRM: Highly Accurate and Sensitive Method for High-Throughput Targeted Proteomics. Anal Chem, 96(25):10219-10227(2024) [pubmed]
Keyword List
submitter keyword: PRM,targeted proteomics, parallel reaction monitoring, absolute quantification
Contact List
Sang-Won Lee
contact affiliationDepartment of Chemistry and Center for ProteoGenome Research, Korea University, Seoul 02841, Republic of Korea
contact emailsw_lee@korea.ac.kr
lab head
Dowoon Nam
contact affiliationKorea University
contact emaildowoon0517@korea.ac.kr
dataset submitter
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2024/08/PXD048271
PRIDE project URI
Repository Record List
[ + ]