Targeted Proteomics VS Discovery Proteomics

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targeted and discovery proteomics

At present, strategies for proteomics research can be divided into discovery proteomics and targeted proteomics. Discovery proteomics is more concerned with protein screening and dynamics, while targeted proteomics focuses more on detec�ng target proteins/pep�des to achieve the absolute quan�fica�on.

SRM / MRM eliminates a large number of interfering ions through two-stage ion selec�on. The chemical background of the mass spectrum is reduced, and the signal-to-noise ra�o of the target detector is significantly improved, thereby achieving high detec�on sensi�vity.

PRM can quan�fy 50 proteins simultaneously in an hour without the use of an�bodies. Comprehensive scanning of product ions can be easily done without selec�ng ion pairs and op�mizing the fragment energy.

Compared with the tradi�onal SRM/MRM technology, the PRM can detect all target ions from the target ion pair fragment detec�on conversion, reducing workload and with higher resolu�on.

SWATH-DIA is suitable for high-throughput large-scale protein quan�ta�ve analysis. The peak informa�on of the MS1 precursor ion and MS2 fragment ion is very complete, so retrospec�ve analysis a�er some �me is necessary. It can be easily operated without grouping. The number of SWATH-DIA quan�ta�ve pep�des has greatly increased, enhancing the number of the corresponding quan�fiable protein and the sequence coverage of the detected protein.

In MSX-DIA, the mass range is divided into much narrower precursor isola�on windows, each of which is usually about 4 m / z wide. All ion and fragment spectra can be collected without losing any informa�on. The data is easy to trace. Even if certain proteins or compounds cannot be found at current levels, they can be traced back in the future.

examples of applications

Targeted proteomics is used for in-depth analysis and quan�ta�ve measurement of selected proteins in biological samples. Informa�on on the protein of interest is required before analysis. Our TPro™ Pla�orm is designed to quan�fy up to 150 proteins with high precision and throughput in a dynamic range of 6 orders of magnitude.

Supplementary tool for ligand binding assay (LBA) in the area of monoclonal an�body (mAb) dose pharmacokine�cs (PK). Systems biology and clinical proteomics research.

Predict transporter-mediated drug clearance and promote drug discovery / development research.

The goal of discovery proteomics is to gather informa�on about all proteins and protein structures in biological samples. With li�le knowledge on the sample, discovery proteomics can iden�fy thousands of proteins and protein structures in one experiment. Our DPro™ Platform can analyze up to 9,000 proteins per sample under different condi�ons and iden�fy significantly regulated proteins.

Host cell protein analysis.

Iden�fica�on of chemical modifica�ons. The workhorse of biomarker discovery.

Drug target discovery.

PROTEOMICS TARGETED V S DISCOVERY
Targeted Proteomics Discovery Proteomics Cells/tissue Sample Protein Extraction Separation Detection Detection Precursor Ion Collision Cell Q1 Q2 Fragment Software Analysis Bioinformatics Analysis Split to Peptides Precursor Ion Precursor Ion Q3 SRM/MRM SWATH MSX-DIA PRM 1 2 4 5 3 Collision Cell Q1 Q2 Fragment Orbitrap Orbitrap 1 3 2 5 4 25Da Precursor Ion Fragmentation Fragmentation Intensity m/z SWATH 1 Scanning Scanning MS/MS Retention Time Retention Time Intensity Intensity Targeted Proteomics Discovery Proteomics characteristics
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