Computational Selection of RNA Aptamer against Angiopoietin-2 and Experimental Evaluation
Angiogenesis plays a decisive role in the growth and spread of cancer and angiopoietin-2 (Ang2) is in the spotlight of studies for its unique role in modulating angiogenesis. The aim of this study was to introduce a computational simulation approach to screen aptamers with high binding ability for A...
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doaj-07e63685dbd64b119a831771d44f5a712020-11-24T23:11:34ZengHindawi LimitedBioMed Research International2314-61332314-61412015-01-01201510.1155/2015/658712658712Computational Selection of RNA Aptamer against Angiopoietin-2 and Experimental EvaluationWen-Pin Hu0Jangam Vikram Kumar1Chun-Jen Huang2Wen-Yih Chen3Department of Biomedical Informatics, Asia University, Taichung City 41354, TaiwanDepartment of Biomedical Informatics, Asia University, Taichung City 41354, TaiwanGraduate Institute of Biomedical Engineering, National Central University, Jhongli 32001, TaiwanDepartment of Chemical and Materials Engineering, National Central University, Jhongli 32001, TaiwanAngiogenesis plays a decisive role in the growth and spread of cancer and angiopoietin-2 (Ang2) is in the spotlight of studies for its unique role in modulating angiogenesis. The aim of this study was to introduce a computational simulation approach to screen aptamers with high binding ability for Ang2. We carried out computational simulations of aptamer-protein interactions by using ZDOCK and ZRANK functions in Discovery Studio 3.5 starting from the available information of aptamers generated through the systematic evolution of ligands by exponential enrichment (SELEX) in the literature. From the best of three aptamers on the basis of ZRANK scores, 189 sequences with two-point mutations were created and simulated with Ang2. Then, we used a surface plasmon resonance (SPR) biosensor to test 3 mutant sequences of high ZRANK scores along with a high and a low affinity binding sequence as reported in the literature. We found a selected RNA aptamer has a higher binding affinity and SPR response than a reported sequence with the highest affinity. This is the first study of in silico selection of aptamers against Ang2 by using the ZRANK scoring function, which should help to increase the efficiency of selecting aptamers with high target-binding ability.http://dx.doi.org/10.1155/2015/658712 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wen-Pin Hu Jangam Vikram Kumar Chun-Jen Huang Wen-Yih Chen |
spellingShingle |
Wen-Pin Hu Jangam Vikram Kumar Chun-Jen Huang Wen-Yih Chen Computational Selection of RNA Aptamer against Angiopoietin-2 and Experimental Evaluation BioMed Research International |
author_facet |
Wen-Pin Hu Jangam Vikram Kumar Chun-Jen Huang Wen-Yih Chen |
author_sort |
Wen-Pin Hu |
title |
Computational Selection of RNA Aptamer against Angiopoietin-2 and Experimental Evaluation |
title_short |
Computational Selection of RNA Aptamer against Angiopoietin-2 and Experimental Evaluation |
title_full |
Computational Selection of RNA Aptamer against Angiopoietin-2 and Experimental Evaluation |
title_fullStr |
Computational Selection of RNA Aptamer against Angiopoietin-2 and Experimental Evaluation |
title_full_unstemmed |
Computational Selection of RNA Aptamer against Angiopoietin-2 and Experimental Evaluation |
title_sort |
computational selection of rna aptamer against angiopoietin-2 and experimental evaluation |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2015-01-01 |
description |
Angiogenesis plays a decisive role in the growth and spread of cancer and angiopoietin-2 (Ang2) is in the spotlight of studies for its unique role in modulating angiogenesis. The aim of this study was to introduce a computational simulation approach to screen aptamers with high binding ability for Ang2. We carried out computational simulations of aptamer-protein interactions by using ZDOCK and ZRANK functions in Discovery Studio 3.5 starting from the available information of aptamers generated through the systematic evolution of ligands by exponential enrichment (SELEX) in the literature. From the best of three aptamers on the basis of ZRANK scores, 189 sequences with two-point mutations were created and simulated with Ang2. Then, we used a surface plasmon resonance (SPR) biosensor to test 3 mutant sequences of high ZRANK scores along with a high and a low affinity binding sequence as reported in the literature. We found a selected RNA aptamer has a higher binding affinity and SPR response than a reported sequence with the highest affinity. This is the first study of in silico selection of aptamers against Ang2 by using the ZRANK scoring function, which should help to increase the efficiency of selecting aptamers with high target-binding ability. |
url |
http://dx.doi.org/10.1155/2015/658712 |
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1725603799009067008 |