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<strong>JIOMICS</strong> | VOL 5 | ISSUE 2 | DECEMBER 2015 | 1-62<br />

JOURNAL OF INTEGRATED OMICS<br />

Journal of Integrated Omics<br />

A METHODOLOGICAL JOURNAL<br />

HTTP://WWW.<strong>JIOMICS</strong>.COM<br />

Special Issue: Proceeding Abstracts of the 4 th International Congress on Analytical Proteomics (ICAP 2015)<br />

Some proteins of possible -clinical interest found in samples of human<br />

intestinal mucus (HIM)<br />

Gómez-Buitrago Paola-Andrea* 1 , González-Correa Carlos-Augusto 1 , Taborda-Ocampo Gonzalo 1 , Acuña-Sornoza Ricardo 2 ,<br />

Santacoloma-Osorio Mario 3 , Zezzi-Arruda Marco-Aurelio 4 .<br />

1<br />

Research Group on Electrical Bio-Impedance, Doctoral Program on Biomedical Sciences, University of Caldas, Manizales, Colombia.<br />

2<br />

Colombian National Coffee Research Center CENICAFE, Chinchiná, Colombia. 3 linical Department, University of Caldas, Manizales,<br />

Colombia. 4 State University of Campinas, Institute of Chemistry, Campinas, Brazil. *Corresponding author: quimicapao@gmail.com<br />

Available Online: 31 December 2015<br />

Abstract<br />

Purpose: To report the identification of some proteins isolated from samples of human intestinal mucus (HIM) with possible clinical<br />

interest.<br />

Experimental description: HIM was collected from six volunteers admitted to a leaning program which included a colon cleansing protocol<br />

and a rectosigmoidoscopy. Protein extraction was achieved by a denaturalization buffer, separation was performed by gel electrophoresis<br />

both with SDS-PAGE and 2D-PAGE. Protein shotgun was done with solution desalinization by SPE and albumin depletion. Digested peptides<br />

were analysed using a NanoAcquity UPLC cromatograph coupled to a HDSM espectrometer, equiped with a NanoESI source. Samples were<br />

injected to a C 18 precolumn with a flow of 5 μL/min water/acetonitrile (97:3) with 0,1% formica cid and then transfered to an analytical column<br />

C 18 and eluted with a flow of 1 μL/min.<br />

Partial results: 1. A methodology for the analysis of HIM from a single person is reported, from the preparation of the patients for the<br />

collection of the sample, till protein characterization of the mucus. This is done using mass spectrometry, using three different techniques: SDS<br />

-PAGE, 2D-PAGE y shotgun; 2. 14 proteins of clinical interest have been identified so far: Annexin A2, Calcium-activated chloride channel<br />

regulator, Chain crystal structure of human calcineurin complexed with cyclosporin A and human cyclophilin, Complement C3, Disulfide<br />

isomerase, Galectin-3 y 4, Inmunoglobulin programmed cell death 1 ligand, LAMTOR3, Muc2, Nuclear Protein 8, RuvB like 2, Tyrosine Protein<br />

phosphatase non receptor type 11 and Zymogen granule membrane protein 16.<br />

Conclusion: The proteomic study of HIM can be a very useful tool for the study of different diseases, not only of those directly related to<br />

the digestive system, bus also many associated with the immune system.<br />

Keywords: electrophoresis, human intestinal mucus, shotgun proteomics.<br />

1-62: 9

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