Artikel: Dual-transgenic BiFC vector systems for protein-protein interaction analysis in plants.
2024 Band 15, Seite(n) 1355568
Abstract: Protein-protein interaction (PPI) play a pivotal role in cellular signal transduction. The bimolecular fluorescence complementation (BiFC) assay offers a rapid and intuitive means to ascertain the localization and interactions of target proteins within ... ...
Abstract | Protein-protein interaction (PPI) play a pivotal role in cellular signal transduction. The bimolecular fluorescence complementation (BiFC) assay offers a rapid and intuitive means to ascertain the localization and interactions of target proteins within living cells. BiFC is based on fluorescence complementation by reconstitution of a functional fluorescent protein by co-expression of N- and C-terminal fragments of this protein. When fusion proteins interact, the N- and C-terminal fragments come into close proximity, leading to the reconstitution of the fluorescent protein. In the conventional approach, the N-terminal and C-terminal fragments of the fluorescent protein are typically expressed using two separate vectors, which largely relies on the efficiency of the transformation of the two vectors in the same cells. Furthermore, issues of vector incompatibility can often result in loss of one plasmid. To address these challenges, we have developed novel dual-transgenic BiFC vectors, designed as |
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Sprache | Englisch |
Erscheinungsdatum | 2024-03-08 |
Erscheinungsland | Switzerland |
Dokumenttyp | Journal Article |
ZDB-ID | 2606823-0 |
ISSN | 1664-8021 |
ISSN | 1664-8021 |
DOI | 10.3389/fgene.2024.1355568 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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