Different techniques for urinary protein analysis of normal and lung cancer patients

Many components in urine are useful in clinical diagnosis and urinary proteins are known as important components to define many diseases such as proteinuria, kidney, bladder and urinary tract diseases. In this study, we focused on the comparison of different sample preparation methods for isolating...

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Main Authors: Tantipaiboonwong P., Sinchaikul S., Sriyam S., Phutrakul S., Chen S.-T.
Format: Conference or Workshop Item
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-16344387536&partnerID=40&md5=a008b95dee75a657bc6cd20a52d248bc
http://cmuir.cmu.ac.th/handle/6653943832/5008
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-50082014-08-30T02:56:03Z Different techniques for urinary protein analysis of normal and lung cancer patients Tantipaiboonwong P. Sinchaikul S. Sriyam S. Phutrakul S. Chen S.-T. Many components in urine are useful in clinical diagnosis and urinary proteins are known as important components to define many diseases such as proteinuria, kidney, bladder and urinary tract diseases. In this study, we focused on the comparison of different sample preparation methods for isolating urinary proteins prior to protein analysis of pooled healthy and lung cancer patient samples. Selective method was used for preliminary investigation of some putative urinary protein markers. Urine samples were passed first through a gel filtration column (PD-10 desalting column) to remove high salts and subsequently concentrated. Remaining interferences were removed by ultrafiltration or four precipitation methods. The analysis of urinary proteins by high-performance liquid chromatography and sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed many similarities in profiles among preparation methods and a few profiles were different between normal and lung cancer patients. In contrast, the results of two-dimensional gel electrophoresis (2-DE) showed more distinctly different protein patterns. Our finding showed that the sequential preparation of urinary proteins by gel filtration and ultrafiltration could retain most urinary proteins which demonstrated the highest protein spots on 2-D gels and able to identify preliminary urinary protein markers related to cancer. Although sequential preparation of urine samples by gel filtration and protein precipitation resulted in low amounts of proteins on 2-D gels, high Mr proteins were easily detected. Therefore, there are alternative choices for urine sample preparation for studying the urinary proteome and identifing urinary protein markers important for further preclinical diagnostic and therapeutic applications. © 2005 WILEY-VCH Verlag GmbH & Co. KGaA. 2014-08-30T02:56:03Z 2014-08-30T02:56:03Z 2005 Conference Paper 16159853 10.1002/pmic.200401143 15693063 PROTC http://www.scopus.com/inward/record.url?eid=2-s2.0-16344387536&partnerID=40&md5=a008b95dee75a657bc6cd20a52d248bc http://cmuir.cmu.ac.th/handle/6653943832/5008 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
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language English
description Many components in urine are useful in clinical diagnosis and urinary proteins are known as important components to define many diseases such as proteinuria, kidney, bladder and urinary tract diseases. In this study, we focused on the comparison of different sample preparation methods for isolating urinary proteins prior to protein analysis of pooled healthy and lung cancer patient samples. Selective method was used for preliminary investigation of some putative urinary protein markers. Urine samples were passed first through a gel filtration column (PD-10 desalting column) to remove high salts and subsequently concentrated. Remaining interferences were removed by ultrafiltration or four precipitation methods. The analysis of urinary proteins by high-performance liquid chromatography and sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed many similarities in profiles among preparation methods and a few profiles were different between normal and lung cancer patients. In contrast, the results of two-dimensional gel electrophoresis (2-DE) showed more distinctly different protein patterns. Our finding showed that the sequential preparation of urinary proteins by gel filtration and ultrafiltration could retain most urinary proteins which demonstrated the highest protein spots on 2-D gels and able to identify preliminary urinary protein markers related to cancer. Although sequential preparation of urine samples by gel filtration and protein precipitation resulted in low amounts of proteins on 2-D gels, high Mr proteins were easily detected. Therefore, there are alternative choices for urine sample preparation for studying the urinary proteome and identifing urinary protein markers important for further preclinical diagnostic and therapeutic applications. © 2005 WILEY-VCH Verlag GmbH & Co. KGaA.
format Conference or Workshop Item
author Tantipaiboonwong P.
Sinchaikul S.
Sriyam S.
Phutrakul S.
Chen S.-T.
spellingShingle Tantipaiboonwong P.
Sinchaikul S.
Sriyam S.
Phutrakul S.
Chen S.-T.
Different techniques for urinary protein analysis of normal and lung cancer patients
author_facet Tantipaiboonwong P.
Sinchaikul S.
Sriyam S.
Phutrakul S.
Chen S.-T.
author_sort Tantipaiboonwong P.
title Different techniques for urinary protein analysis of normal and lung cancer patients
title_short Different techniques for urinary protein analysis of normal and lung cancer patients
title_full Different techniques for urinary protein analysis of normal and lung cancer patients
title_fullStr Different techniques for urinary protein analysis of normal and lung cancer patients
title_full_unstemmed Different techniques for urinary protein analysis of normal and lung cancer patients
title_sort different techniques for urinary protein analysis of normal and lung cancer patients
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-16344387536&partnerID=40&md5=a008b95dee75a657bc6cd20a52d248bc
http://cmuir.cmu.ac.th/handle/6653943832/5008
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