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Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental in vitro validation
Nuclear translocation of large proteins is mediated through karyopherins, carrier proteins recognizing specific motifs of cargo proteins, known as nuclear localization signals (NLS). However, only few NLS signals have been reported until now. In the present work, NLS signals for Importins 4 and 5 we...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Research Network of Computational and Structural Biotechnology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646746/ https://www.ncbi.nlm.nih.gov/pubmed/36382187 http://dx.doi.org/10.1016/j.csbj.2022.10.015 |
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author | Panagiotopoulos, Athanasios A. Kalyvianaki, Konstantina Tsodoulou, Paraskevi K. Darivianaki, Maria N. Dellis, Dimitris Notas, George Daskalakis, Vangelis Theodoropoulos, Panayiotis A. Panagiotidis, Christos Α. Castanas, Elias Kampa, Marilena |
author_facet | Panagiotopoulos, Athanasios A. Kalyvianaki, Konstantina Tsodoulou, Paraskevi K. Darivianaki, Maria N. Dellis, Dimitris Notas, George Daskalakis, Vangelis Theodoropoulos, Panayiotis A. Panagiotidis, Christos Α. Castanas, Elias Kampa, Marilena |
author_sort | Panagiotopoulos, Athanasios A. |
collection | PubMed |
description | Nuclear translocation of large proteins is mediated through karyopherins, carrier proteins recognizing specific motifs of cargo proteins, known as nuclear localization signals (NLS). However, only few NLS signals have been reported until now. In the present work, NLS signals for Importins 4 and 5 were identified through an unsupervised in silico approach, followed by experimental in vitro validation. The sequences LPPRS(G/P)P and KP(K/Y)LV were identified and are proposed as recognition motifs for Importins 4 and 5 binding, respectively. They are involved in the trafficking of important proteins into the nucleus. These sequences were validated in the breast cancer cell line T47D, which expresses both Importins 4 and 5. Elucidating the complex relationships of the nuclear transporters and their cargo proteins is very important in better understanding the mechanism of nuclear transport of proteins and laying the foundation for the development of novel therapeutics, targeting specific importins. |
format | Online Article Text |
id | pubmed-9646746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Research Network of Computational and Structural Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-96467462022-11-14 Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental in vitro validation Panagiotopoulos, Athanasios A. Kalyvianaki, Konstantina Tsodoulou, Paraskevi K. Darivianaki, Maria N. Dellis, Dimitris Notas, George Daskalakis, Vangelis Theodoropoulos, Panayiotis A. Panagiotidis, Christos Α. Castanas, Elias Kampa, Marilena Comput Struct Biotechnol J Research Article Nuclear translocation of large proteins is mediated through karyopherins, carrier proteins recognizing specific motifs of cargo proteins, known as nuclear localization signals (NLS). However, only few NLS signals have been reported until now. In the present work, NLS signals for Importins 4 and 5 were identified through an unsupervised in silico approach, followed by experimental in vitro validation. The sequences LPPRS(G/P)P and KP(K/Y)LV were identified and are proposed as recognition motifs for Importins 4 and 5 binding, respectively. They are involved in the trafficking of important proteins into the nucleus. These sequences were validated in the breast cancer cell line T47D, which expresses both Importins 4 and 5. Elucidating the complex relationships of the nuclear transporters and their cargo proteins is very important in better understanding the mechanism of nuclear transport of proteins and laying the foundation for the development of novel therapeutics, targeting specific importins. Research Network of Computational and Structural Biotechnology 2022-10-26 /pmc/articles/PMC9646746/ /pubmed/36382187 http://dx.doi.org/10.1016/j.csbj.2022.10.015 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Panagiotopoulos, Athanasios A. Kalyvianaki, Konstantina Tsodoulou, Paraskevi K. Darivianaki, Maria N. Dellis, Dimitris Notas, George Daskalakis, Vangelis Theodoropoulos, Panayiotis A. Panagiotidis, Christos Α. Castanas, Elias Kampa, Marilena Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental in vitro validation |
title | Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental in vitro validation |
title_full | Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental in vitro validation |
title_fullStr | Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental in vitro validation |
title_full_unstemmed | Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental in vitro validation |
title_short | Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental in vitro validation |
title_sort | recognition motifs for importin 4 [(l)pprs(g/p)p] and importin 5 [kp(k/y)lv] binding, identified by bio-informatic simulation and experimental in vitro validation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646746/ https://www.ncbi.nlm.nih.gov/pubmed/36382187 http://dx.doi.org/10.1016/j.csbj.2022.10.015 |
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