JIOMICS
JIOMICS Internacional
JIOMICS Internacional
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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 />
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