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...

Full description

Bibliographic Details
Main Authors: Wen-Pin Hu, Jangam Vikram Kumar, Chun-Jen Huang, Wen-Yih Chen
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2015/658712
id doaj-07e63685dbd64b119a831771d44f5a71
record_format Article
spelling 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
work_keys_str_mv AT wenpinhu computationalselectionofrnaaptameragainstangiopoietin2andexperimentalevaluation
AT jangamvikramkumar computationalselectionofrnaaptameragainstangiopoietin2andexperimentalevaluation
AT chunjenhuang computationalselectionofrnaaptameragainstangiopoietin2andexperimentalevaluation
AT wenyihchen computationalselectionofrnaaptameragainstangiopoietin2andexperimentalevaluation
_version_ 1725603799009067008