A sample preparation workflow for adipose tissue shotgun proteomics and proteogenomics

Author:

Khudyakov Jane I.12ORCID,Deyarmin Jared S.1,Hekman Ryan M.1,Pujade Busqueta Laura1,Maan Rasool1,Mody Melony J.1,Banerjee Reeti1,Crocker Daniel E.3ORCID,Champagne Cory D.2ORCID

Affiliation:

1. University of the Pacific, Stockton, CA, USA

2. National Marine Mammal Foundation, San Diego, CA, USA

3. Sonoma State University, Rohnert Park, CA, USA

Abstract

Animals with large adipose stores, such as marine mammals, may provide insights into evolution and function of this multifunctional tissue in health and disease. In the absence of sequenced genomes, molecular information can be rapidly obtained by proteomics and transcriptomics, but their application to adipose tissue is hindered by low nucleic acid and protein yields. We sequenced and compared proteomes isolated from blubber of four elephant seals using phenol and guanidine thiocyanate (Qiazol) or detergent (sodium deoxycholate) buffer. Qiazol recovered more subcellular proteins such as metabolic enzymes, in addition to extracting RNA, facilitating proteogenomic analyses of small lipid-rich tissue biopsies. We also compared proteomics data analysis platforms and found that de novo peptide sequencing improved protein identification sensitivity compared to database search alone. We report sample preparation and data analysis workflows for proteogenomics and a proteome of elephant seal blubber containing 2,678 proteins, including many of interest for further functional studies.

Funder

Office of Naval Research

Publisher

The Company of Biologists

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

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