Optimisation of urine sample preparation for shotgun proteomics

Urine reflects the renal function and urinary and kidney systems, but it may also reflect the presence of cancer in other parts of the body. Urine also has potential for providing prognostic information during therapeutic treatments thanks to non-invasive monitoring. A quick and reproducible protein...

Full description

Bibliographic Details
Main Authors: Tkáčiková Soňa, Talian Ivan, Sabo Ján
Format: Article
Language:English
Published: De Gruyter 2020-08-01
Series:Open Chemistry
Subjects:
Online Access:https://doi.org/10.1515/chem-2020-0150
id doaj-2379d4da8ea54fcb8ed444a7be6fa78b
record_format Article
spelling doaj-2379d4da8ea54fcb8ed444a7be6fa78b2021-09-06T19:19:37ZengDe GruyterOpen Chemistry2391-54202020-08-0118185085610.1515/chem-2020-0150chem-2020-0150Optimisation of urine sample preparation for shotgun proteomicsTkáčiková Soňa0Talian Ivan1Sabo Ján2Department of Medical and Clinical Biophysics, Faculty of Medicine, Pavol Jozef Šafárik University in Košice, tr. SNP 1, 040 11 Košice, SlovakiaDepartment of Medical and Clinical Biophysics, Faculty of Medicine, Pavol Jozef Šafárik University in Košice, tr. SNP 1, 040 11 Košice, SlovakiaDepartment of Medical and Clinical Biophysics, Faculty of Medicine, Pavol Jozef Šafárik University in Košice, tr. SNP 1, 040 11 Košice, SlovakiaUrine reflects the renal function and urinary and kidney systems, but it may also reflect the presence of cancer in other parts of the body. Urine also has potential for providing prognostic information during therapeutic treatments thanks to non-invasive monitoring. A quick and reproducible protein purification procedure is essential to allow data comparison between proteomic studies in urine biomarker discovery. The article describes a simple, reproducible and cheap sample preparation procedure with a maximum protein yield (400 µg) obtained from only 10 mL of urine utilising cut-off filter desalting and digestion. The reported procedure removes yellowish background coloration residues and thus prevents the errors in spectrophotometric protein concentration determination. Different extraction solvents used in the presented procedure point to the possibility of partial elimination of abundant proteins (albumin and keratin family), as well as to the improvement of the sequence coverage of proteins identified, which helps to reveal changes in the urinary proteome. With this workflow, proteins can be easily obtained on standard laboratory equipment within 3 h. Data are available via ProteomeXchange with identifier PXD019738.https://doi.org/10.1515/chem-2020-0150urineproteomicsprotein extractionmass spectrometry.
collection DOAJ
language English
format Article
sources DOAJ
author Tkáčiková Soňa
Talian Ivan
Sabo Ján
spellingShingle Tkáčiková Soňa
Talian Ivan
Sabo Ján
Optimisation of urine sample preparation for shotgun proteomics
Open Chemistry
urine
proteomics
protein extraction
mass spectrometry.
author_facet Tkáčiková Soňa
Talian Ivan
Sabo Ján
author_sort Tkáčiková Soňa
title Optimisation of urine sample preparation for shotgun proteomics
title_short Optimisation of urine sample preparation for shotgun proteomics
title_full Optimisation of urine sample preparation for shotgun proteomics
title_fullStr Optimisation of urine sample preparation for shotgun proteomics
title_full_unstemmed Optimisation of urine sample preparation for shotgun proteomics
title_sort optimisation of urine sample preparation for shotgun proteomics
publisher De Gruyter
series Open Chemistry
issn 2391-5420
publishDate 2020-08-01
description Urine reflects the renal function and urinary and kidney systems, but it may also reflect the presence of cancer in other parts of the body. Urine also has potential for providing prognostic information during therapeutic treatments thanks to non-invasive monitoring. A quick and reproducible protein purification procedure is essential to allow data comparison between proteomic studies in urine biomarker discovery. The article describes a simple, reproducible and cheap sample preparation procedure with a maximum protein yield (400 µg) obtained from only 10 mL of urine utilising cut-off filter desalting and digestion. The reported procedure removes yellowish background coloration residues and thus prevents the errors in spectrophotometric protein concentration determination. Different extraction solvents used in the presented procedure point to the possibility of partial elimination of abundant proteins (albumin and keratin family), as well as to the improvement of the sequence coverage of proteins identified, which helps to reveal changes in the urinary proteome. With this workflow, proteins can be easily obtained on standard laboratory equipment within 3 h. Data are available via ProteomeXchange with identifier PXD019738.
topic urine
proteomics
protein extraction
mass spectrometry.
url https://doi.org/10.1515/chem-2020-0150
work_keys_str_mv AT tkacikovasona optimisationofurinesamplepreparationforshotgunproteomics
AT talianivan optimisationofurinesamplepreparationforshotgunproteomics
AT sabojan optimisationofurinesamplepreparationforshotgunproteomics
_version_ 1717778142625529856