Cargando…

SRM-MS Method Development for Hepcidin-25 Peptide

As advanced mass spectrometry- (MS-) based hepcidin analysis offers to overcome the limitations in analytical methods using antihepcidin, further improvement of MS detection sensitivity for the peptide may enhance the diagnostic value of the hepcidin for various iron-related disorders. Here, improve...

Descripción completa

Detalles Bibliográficos
Autores principales: Cho, Kyung-Cho, Cho, Byoung-Kyu, Jung, Jin Woo, Lee, Ye Ji, Lee, Eun Bong, Yi, Eugene C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022310/
https://www.ncbi.nlm.nih.gov/pubmed/30013808
http://dx.doi.org/10.1155/2018/9653747
_version_ 1783335652004200448
author Cho, Kyung-Cho
Cho, Byoung-Kyu
Jung, Jin Woo
Lee, Ye Ji
Lee, Eun Bong
Yi, Eugene C.
author_facet Cho, Kyung-Cho
Cho, Byoung-Kyu
Jung, Jin Woo
Lee, Ye Ji
Lee, Eun Bong
Yi, Eugene C.
author_sort Cho, Kyung-Cho
collection PubMed
description As advanced mass spectrometry- (MS-) based hepcidin analysis offers to overcome the limitations in analytical methods using antihepcidin, further improvement of MS detection sensitivity for the peptide may enhance the diagnostic value of the hepcidin for various iron-related disorders. Here, improved MS detection sensitivity of hepcidin has been achieved by reducing the disulfide bonds in hepcidin, by which proton accessibility increased, compared to the intact hepcidin peptide. Comparing the ionization efficiencies of reduced and nonreduced forms of hepcidin, the reduced form of hepcidin showed an increase in ionization efficiency more than two times compared to the nonreduced form of hepcidin. We also demonstrated improved detection sensitivity of the peptide in SRM assay. We observed a significant improvement of detection sensitivity at the triple-quadrupole MS platform, that the ionization efficiency increased at least twice more, and that the limit of detection (LOD) increased more than 10 times in the concentration ranges of 1 fmol to 10 fmol of hepcidin. In this study, we demonstrated the usefulness of the hepcidin modification for overall enhancement of the ionization efficiencies of the hepcidin peptide in the MS-based quantitative measurement assay.
format Online
Article
Text
id pubmed-6022310
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-60223102018-07-16 SRM-MS Method Development for Hepcidin-25 Peptide Cho, Kyung-Cho Cho, Byoung-Kyu Jung, Jin Woo Lee, Ye Ji Lee, Eun Bong Yi, Eugene C. J Anal Methods Chem Research Article As advanced mass spectrometry- (MS-) based hepcidin analysis offers to overcome the limitations in analytical methods using antihepcidin, further improvement of MS detection sensitivity for the peptide may enhance the diagnostic value of the hepcidin for various iron-related disorders. Here, improved MS detection sensitivity of hepcidin has been achieved by reducing the disulfide bonds in hepcidin, by which proton accessibility increased, compared to the intact hepcidin peptide. Comparing the ionization efficiencies of reduced and nonreduced forms of hepcidin, the reduced form of hepcidin showed an increase in ionization efficiency more than two times compared to the nonreduced form of hepcidin. We also demonstrated improved detection sensitivity of the peptide in SRM assay. We observed a significant improvement of detection sensitivity at the triple-quadrupole MS platform, that the ionization efficiency increased at least twice more, and that the limit of detection (LOD) increased more than 10 times in the concentration ranges of 1 fmol to 10 fmol of hepcidin. In this study, we demonstrated the usefulness of the hepcidin modification for overall enhancement of the ionization efficiencies of the hepcidin peptide in the MS-based quantitative measurement assay. Hindawi 2018-06-14 /pmc/articles/PMC6022310/ /pubmed/30013808 http://dx.doi.org/10.1155/2018/9653747 Text en Copyright © 2018 Kyung-Cho Cho et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Cho, Kyung-Cho
Cho, Byoung-Kyu
Jung, Jin Woo
Lee, Ye Ji
Lee, Eun Bong
Yi, Eugene C.
SRM-MS Method Development for Hepcidin-25 Peptide
title SRM-MS Method Development for Hepcidin-25 Peptide
title_full SRM-MS Method Development for Hepcidin-25 Peptide
title_fullStr SRM-MS Method Development for Hepcidin-25 Peptide
title_full_unstemmed SRM-MS Method Development for Hepcidin-25 Peptide
title_short SRM-MS Method Development for Hepcidin-25 Peptide
title_sort srm-ms method development for hepcidin-25 peptide
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022310/
https://www.ncbi.nlm.nih.gov/pubmed/30013808
http://dx.doi.org/10.1155/2018/9653747
work_keys_str_mv AT chokyungcho srmmsmethoddevelopmentforhepcidin25peptide
AT chobyoungkyu srmmsmethoddevelopmentforhepcidin25peptide
AT jungjinwoo srmmsmethoddevelopmentforhepcidin25peptide
AT leeyeji srmmsmethoddevelopmentforhepcidin25peptide
AT leeeunbong srmmsmethoddevelopmentforhepcidin25peptide
AT yieugenec srmmsmethoddevelopmentforhepcidin25peptide