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Editorial
. 2017 Dec;9(12):4867-4870.
doi: 10.21037/jtd.2017.11.73.

Optogenetic tools for cell biological applications

Affiliations
Editorial

Optogenetic tools for cell biological applications

Abhirup Mukherjee et al. J Thorac Dis. 2017 Dec.
No abstract available

PubMed Disclaimer

Conflict of interest statement

Conflicts of Interest: The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Representative schematic of the BphP1-Q-PAS1 system. Protein size is indicated by relative size of bars. Sample proteins A and B are drawn to a scale of 500 amino acids. (A) Light-induced reversible dimerization between BphP1 (red) and Q-PAS1 (beige) leads to interaction of fused domains (grey); (B) schematic showing domain structures of PpsR2 and Q-PAS1. Adapted with permission from Redchuk et al. (8).
Figure 2
Figure 2
Tridirectional subcellular translocation of protein and spectral multiplexing with blue and NIR-light using the AsLOV2 and BphP1-Q-PAS1 systems. (A) Schematic showing blue-light-induced nuclear translocation and NIR-light-induced plasma membrane translocation of attached protein, mCherry (red); (B) live fluorescence image showing sequential translocation of mCherry to the nucleus and plasma membrane in response to indicated illumination with intermittent dark relaxation periods. Adapted with permission from Redchuk et al. (8). NIR, near-infrared.

Comment on

References

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