Proteomics evaluation of five economical commercial abundant protein depletion kits for enrichment of diseases‐specific biomarkers from blood serum

Author:

Ahsan Nagib12ORCID,Fornelli Luca13,Najar Fares Z.4,Gamagedara Sanjeewa5,Hossan Mohammad Robiul6,Rao R. Shyama Prasad7,Punyamurtula Ujwal8,Bauer Andrew9,Yang Zhibo1,Foster Steven B.12,Kane Maureen A.10

Affiliation:

1. Department of Chemistry and Biochemistry University of Oklahoma Norman Oklahoma USA

2. Mass Spectrometry Proteomics and Metabolomics Core Facility Stephenson Life Sciences Research Center The University of Oklahoma Norman Oklahoma USA

3. Department of Biology University of Oklahoma Norman Oklahoma USA

4. High‐Performance Computing Center (HPCC) Oklahoma State University Stillwater Oklahoma USA

5. Department of Chemistry University of Central Oklahoma Edmond Oklahoma USA

6. School of Engineering University of Central Oklahoma Edmond Oklahoma USA

7. Center for Bioinformatics NITTE deemed to be University Mangaluru Karnataka India

8. Department of Cancer Biology Dana‐Farber Cancer Institute Boston Massachusetts USA

9. Department of Neurosurgery University of Oklahoma‐Health Science Center Oklahoma Oklahoma USA

10. Department of Pharmaceutical Sciences University of Maryland Baltimore Maryland USA

Abstract

AbstractBlood serum is arguably the most analyzed biofluid for disease prediction and diagnosis. Herein, we benchmarked five different serum abundant protein depletion (SAPD) kits with regard to the identification of disease‐specific biomarkers in human serum using bottom‐up proteomics. As expected, the IgG removal efficiency among the SAPD kits is highly variable, ranging from 70% to 93%. A pairwise comparison of database search results showed a 10%–19% variation in protein identification among the kits. Immunocapturing‐based SAPD kits against IgG and albumin outperformed the others in the removal of these two abundant proteins. Conversely, non‐antibody‐based methods (i.e., kits using ion exchange resins) and kits leveraging a multi‐antibody approach were proven to be less efficient in depleting IgG/albumin from samples but led to the highest number of identified peptides. Notably, our results indicate that different cancer biomarkers could be enriched up to 10% depending on the utilized SAPD kit compared with the undepleted sample. Additionally, functional analysis of the bottom‐up proteomic results revealed that different SAPD kits enrich distinct disease‐ and pathway‐specific protein sets. Overall, our study emphasizes that a careful selection of the appropriate commercial SAPD kit is crucial for the analysis of disease biomarkers in serum by shotgun proteomics.

Funder

National Science Foundation

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

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