Cargando…
Utilizing Quantitative Proteomics to Identify Species-Specific Protein Therapeutic Targets for the Treatment of Leishmaniasis
[Image: see text] Leishmaniasis is a tropical disease caused by Leishmania parasites, which are transmitted through the bites of infected sandflies. We focused on the emergence of leishmaniasis in Thailand caused by a species (Leishmania orientalis). Treatment by chemotherapy is not effective agains...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026083/ https://www.ncbi.nlm.nih.gov/pubmed/35474788 http://dx.doi.org/10.1021/acsomega.1c05792 |
_version_ | 1784691036393570304 |
---|---|
author | Krobthong, Sucheewin Yingchutrakul, Yodying Samutrtai, Pawitrabhorn Hitakarun, Atitaya Siripattanapipong, Suradej Leelayoova, Saovanee Mungthin, Mathirut Choowongkomon, Kiattawee |
author_facet | Krobthong, Sucheewin Yingchutrakul, Yodying Samutrtai, Pawitrabhorn Hitakarun, Atitaya Siripattanapipong, Suradej Leelayoova, Saovanee Mungthin, Mathirut Choowongkomon, Kiattawee |
author_sort | Krobthong, Sucheewin |
collection | PubMed |
description | [Image: see text] Leishmaniasis is a tropical disease caused by Leishmania parasites, which are transmitted through the bites of infected sandflies. We focused on the emergence of leishmaniasis in Thailand caused by a species (Leishmania orientalis). Treatment by chemotherapy is not effective against L. orientalis. Hence, we intended to solve this issue using a proteomics approach to investigate protein profiles and in silico analysis for the identification of antigenic proteins from L. orientalis, Leishmania martiniquensis, and Leishmania donovani. Using principal component analysis (PCA), protein profile comparisons indicated that different species of Leishmania are different at the protein level. Proteomics analysis identified 6099 proteins. Among these proteins, 1065 proteins were used for further analysis. There were 16 proteins that were promising candidates for therapeutic aspects as they were abundantly expressed and common to all species. In silico analysis of protein’s antigenicity revealed that eight proteins had the potential for the development of antigenic molecules. Protein profile information and these antigenic proteins may play key roles in the pathogeny of leishmaniasis and can be used as novel therapeutic targets against leishmaniasis in the future. |
format | Online Article Text |
id | pubmed-9026083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90260832022-04-25 Utilizing Quantitative Proteomics to Identify Species-Specific Protein Therapeutic Targets for the Treatment of Leishmaniasis Krobthong, Sucheewin Yingchutrakul, Yodying Samutrtai, Pawitrabhorn Hitakarun, Atitaya Siripattanapipong, Suradej Leelayoova, Saovanee Mungthin, Mathirut Choowongkomon, Kiattawee ACS Omega [Image: see text] Leishmaniasis is a tropical disease caused by Leishmania parasites, which are transmitted through the bites of infected sandflies. We focused on the emergence of leishmaniasis in Thailand caused by a species (Leishmania orientalis). Treatment by chemotherapy is not effective against L. orientalis. Hence, we intended to solve this issue using a proteomics approach to investigate protein profiles and in silico analysis for the identification of antigenic proteins from L. orientalis, Leishmania martiniquensis, and Leishmania donovani. Using principal component analysis (PCA), protein profile comparisons indicated that different species of Leishmania are different at the protein level. Proteomics analysis identified 6099 proteins. Among these proteins, 1065 proteins were used for further analysis. There were 16 proteins that were promising candidates for therapeutic aspects as they were abundantly expressed and common to all species. In silico analysis of protein’s antigenicity revealed that eight proteins had the potential for the development of antigenic molecules. Protein profile information and these antigenic proteins may play key roles in the pathogeny of leishmaniasis and can be used as novel therapeutic targets against leishmaniasis in the future. American Chemical Society 2022-04-04 /pmc/articles/PMC9026083/ /pubmed/35474788 http://dx.doi.org/10.1021/acsomega.1c05792 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Krobthong, Sucheewin Yingchutrakul, Yodying Samutrtai, Pawitrabhorn Hitakarun, Atitaya Siripattanapipong, Suradej Leelayoova, Saovanee Mungthin, Mathirut Choowongkomon, Kiattawee Utilizing Quantitative Proteomics to Identify Species-Specific Protein Therapeutic Targets for the Treatment of Leishmaniasis |
title | Utilizing Quantitative Proteomics to Identify Species-Specific
Protein Therapeutic Targets for the Treatment of Leishmaniasis |
title_full | Utilizing Quantitative Proteomics to Identify Species-Specific
Protein Therapeutic Targets for the Treatment of Leishmaniasis |
title_fullStr | Utilizing Quantitative Proteomics to Identify Species-Specific
Protein Therapeutic Targets for the Treatment of Leishmaniasis |
title_full_unstemmed | Utilizing Quantitative Proteomics to Identify Species-Specific
Protein Therapeutic Targets for the Treatment of Leishmaniasis |
title_short | Utilizing Quantitative Proteomics to Identify Species-Specific
Protein Therapeutic Targets for the Treatment of Leishmaniasis |
title_sort | utilizing quantitative proteomics to identify species-specific
protein therapeutic targets for the treatment of leishmaniasis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026083/ https://www.ncbi.nlm.nih.gov/pubmed/35474788 http://dx.doi.org/10.1021/acsomega.1c05792 |
work_keys_str_mv | AT krobthongsucheewin utilizingquantitativeproteomicstoidentifyspeciesspecificproteintherapeutictargetsforthetreatmentofleishmaniasis AT yingchutrakulyodying utilizingquantitativeproteomicstoidentifyspeciesspecificproteintherapeutictargetsforthetreatmentofleishmaniasis AT samutrtaipawitrabhorn utilizingquantitativeproteomicstoidentifyspeciesspecificproteintherapeutictargetsforthetreatmentofleishmaniasis AT hitakarunatitaya utilizingquantitativeproteomicstoidentifyspeciesspecificproteintherapeutictargetsforthetreatmentofleishmaniasis AT siripattanapipongsuradej utilizingquantitativeproteomicstoidentifyspeciesspecificproteintherapeutictargetsforthetreatmentofleishmaniasis AT leelayoovasaovanee utilizingquantitativeproteomicstoidentifyspeciesspecificproteintherapeutictargetsforthetreatmentofleishmaniasis AT mungthinmathirut utilizingquantitativeproteomicstoidentifyspeciesspecificproteintherapeutictargetsforthetreatmentofleishmaniasis AT choowongkomonkiattawee utilizingquantitativeproteomicstoidentifyspeciesspecificproteintherapeutictargetsforthetreatmentofleishmaniasis |