Publication:
Syringe-push membrane absorption as a simple rapid method of urine preparation for clinical proteomics

dc.contributor.authorSomchai Chutipongtanateen_US
dc.contributor.authorChannarong Changtongen_US
dc.contributor.authorChurat Weeraphanen_US
dc.contributor.authorSuradej Hongengen_US
dc.contributor.authorChantragan Srisomsapen_US
dc.contributor.authorJisnuson Svastien_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherChulabhorn Graduate Instituteen_US
dc.date.accessioned2018-11-23T09:49:11Z
dc.date.available2018-11-23T09:49:11Z
dc.date.issued2015-01-01en_US
dc.description.abstract© 2015 Chutipongtanate et al. Background: The analysis of urinary proteome might reveal biomarkers of clinical value. However, current methods of urine preparation for down-stream proteomic analysis are complicated, time-consuming, and/or expensive. This study aims to develop a robust, simple, inexpensive and readily accessible urine preparation method to facilitate clinical proteomic workflow. Result: Syringe-push membrane absorption (SPMA) was successfully developed by a combination of 5-ml medical syringe and protein-absorbable membrane. Comparing three membranes i.e., nitrocellulose, polyvinylidene difluoride (PVDF) and Whatman no.1, nitrocellulose combined with SPMA (nitrocellulose-SPMA) provided the greatest quality of proteome profile as demonstrated by 2-DE. The quality of the proteome profile and the performance of nitrocellulose- SPMA were systematically compared with three current methods of urine preparation (i.e., ultrafiltration, dialysis/ lyophilization and precipitation). While different methods of urine preparation provided comparable proteome quality, nitrocellulose-SPMA had better working performance due to acceptable recovery yield, less workload, short working time, high accessibility and low unit cost. In addition, protein absorbed on nitrocellulose harvested from the SPMA procedure could be stored as a dried membrane at room temperature for at least 1-month without protein degradation or modification. Conclusions: SPMA is a simple rapid method of preparing urine for downstream proteomic analysis. Because of it is highly accessible and has long storage duration, this technique holds potential benefit for large-scale multi-center research and future development of clinical investigation based upon urinary proteomic analysis.en_US
dc.identifier.citationClinical Proteomics. Vol.12, No.1 (2015)en_US
dc.identifier.doi10.1186/s12014-015-9087-4en_US
dc.identifier.issn15590275en_US
dc.identifier.issn15426416en_US
dc.identifier.other2-s2.0-84988733161en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/35585
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84988733161&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleSyringe-push membrane absorption as a simple rapid method of urine preparation for clinical proteomicsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84988733161&origin=inwarden_US

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