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  4. 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
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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

Journal
Computational and Structural Biotechnology Journal
Date Issued
2022
Author(s)
Panagiotopoulos, Athanasios  
Kalyvianaki, Konstantina  
Tsodoulou, Paraskevi K  
Darivianaki, Maria N  
Dellis, Dimitris  
Notas, George  
Daskalakis, Vangelis  
Theodoropoulos, Panayiotis A  
Panagiotidis, Christos Α  
Castanas, Elias  
Kampa, Marilena  
DOI
10.1016/j.csbj.2022.10.015
Abstract
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.
Subjects

IPO4

Importin 4

Importin 5

Karyopherins

Nuclear localization ...

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Daskalakis 3.pdf

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1e878d8d839546553e66f3c3f3ab87b6

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