Immobilization of amino acids leucine and glycine on polypyrrole for biosensor applications: A density functional theory study
Adsorption based on the immobilization of amino acids, i.e. leucine and glycine, on the surface of undoped polypyrrole (Ppy) is investigated. Calculations are done based on density functional theory using Gaussian03 software and applying GGA with 6-31G(d) basis set and exchange-correlation model of...
Saved in:
Main Authors: | , , , , , , , |
---|---|
Format: | text |
Published: |
Animo Repository
2011
|
Subjects: | |
Online Access: | https://animorepository.dlsu.edu.ph/faculty_research/1425 https://animorepository.dlsu.edu.ph/context/faculty_research/article/2424/type/native/viewcontent |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | De La Salle University |
id |
oai:animorepository.dlsu.edu.ph:faculty_research-2424 |
---|---|
record_format |
eprints |
spelling |
oai:animorepository.dlsu.edu.ph:faculty_research-24242021-06-28T02:10:16Z Immobilization of amino acids leucine and glycine on polypyrrole for biosensor applications: A density functional theory study Dipojono, Hermawan K. Safitri, Irma Nugraha, Budi, Eko Mursito Nuryanti, Saputro, Adhitya G. David, Melanie Y. Kasai, Hideaki Adsorption based on the immobilization of amino acids, i.e. leucine and glycine, on the surface of undoped polypyrrole (Ppy) is investigated. Calculations are done based on density functional theory using Gaussian03 software and applying GGA with 6-31G(d) basis set and exchange-correlation model of PBE (Perdew, Burke, Ernzerhof) level of theory. The energy of the Ppy doped with amino acids are minimized with respect to the orientation and distance of the amino acids to the Ppy. Neutral leucine carboxyl shows greater binding energy as compared to that other leucine configurations. It has adsorption energy of 0.25 eV at optimum distance of 2.2 Å from the surface of Ppy. As for the glycine, the zwitterionic carboxyl exhibits the strongest binding energy among other glycine configurations. It has adsorption energy of 0.76 Ev at optimum distance of 1.7 Å from the surface of Ppy. The adsorption processes for both amino acids should proceed easily because the activation barriers are either absent or very small. 2011-01-01T08:00:00Z text text/html https://animorepository.dlsu.edu.ph/faculty_research/1425 https://animorepository.dlsu.edu.ph/context/faculty_research/article/2424/type/native/viewcontent Faculty Research Work Animo Repository Amino acids Leucine Glycine Pyrroles Biosensors Density functionals Adsorption Physics |
institution |
De La Salle University |
building |
De La Salle University Library |
continent |
Asia |
country |
Philippines Philippines |
content_provider |
De La Salle University Library |
collection |
DLSU Institutional Repository |
topic |
Amino acids Leucine Glycine Pyrroles Biosensors Density functionals Adsorption Physics |
spellingShingle |
Amino acids Leucine Glycine Pyrroles Biosensors Density functionals Adsorption Physics Dipojono, Hermawan K. Safitri, Irma Nugraha, Budi, Eko Mursito Nuryanti, Saputro, Adhitya G. David, Melanie Y. Kasai, Hideaki Immobilization of amino acids leucine and glycine on polypyrrole for biosensor applications: A density functional theory study |
description |
Adsorption based on the immobilization of amino acids, i.e. leucine and glycine, on the surface of undoped polypyrrole (Ppy) is investigated. Calculations are done based on density functional theory using Gaussian03 software and applying GGA with 6-31G(d) basis set and exchange-correlation model of PBE (Perdew, Burke, Ernzerhof) level of theory. The energy of the Ppy doped with amino acids are minimized with respect to the orientation and distance of the amino acids to the Ppy. Neutral leucine carboxyl shows greater binding energy as compared to that other leucine configurations. It has adsorption energy of 0.25 eV at optimum distance of 2.2 Å from the surface of Ppy. As for the glycine, the zwitterionic carboxyl exhibits the strongest binding energy among other glycine configurations. It has adsorption energy of 0.76 Ev at optimum distance of 1.7 Å from the surface of Ppy. The adsorption processes for both amino acids should proceed easily because the activation barriers are either absent or very small. |
format |
text |
author |
Dipojono, Hermawan K. Safitri, Irma Nugraha, Budi, Eko Mursito Nuryanti, Saputro, Adhitya G. David, Melanie Y. Kasai, Hideaki |
author_facet |
Dipojono, Hermawan K. Safitri, Irma Nugraha, Budi, Eko Mursito Nuryanti, Saputro, Adhitya G. David, Melanie Y. Kasai, Hideaki |
author_sort |
Dipojono, Hermawan K. |
title |
Immobilization of amino acids leucine and glycine on polypyrrole for biosensor applications: A density functional theory study |
title_short |
Immobilization of amino acids leucine and glycine on polypyrrole for biosensor applications: A density functional theory study |
title_full |
Immobilization of amino acids leucine and glycine on polypyrrole for biosensor applications: A density functional theory study |
title_fullStr |
Immobilization of amino acids leucine and glycine on polypyrrole for biosensor applications: A density functional theory study |
title_full_unstemmed |
Immobilization of amino acids leucine and glycine on polypyrrole for biosensor applications: A density functional theory study |
title_sort |
immobilization of amino acids leucine and glycine on polypyrrole for biosensor applications: a density functional theory study |
publisher |
Animo Repository |
publishDate |
2011 |
url |
https://animorepository.dlsu.edu.ph/faculty_research/1425 https://animorepository.dlsu.edu.ph/context/faculty_research/article/2424/type/native/viewcontent |
_version_ |
1703981052552282112 |