Correlating in Vitro and in Vivo Activities of Light-Inducible Dimers: A Cellular Optogenetics Guide.
Correlating in Vitro and in Vivo Activities of Light-Inducible Dimers: A Cellular Optogenetics Guide.
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DOI:
10.1021/acssynbio.5b00119
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发表时间:
2016-01-15
影响因子:
4.7
通讯作者:
Kuhlman B
中科院分区:
文献类型:
--
作者:
Hallett RA;Zimmerman SP;Yumerefendi H;Bear JE;Kuhlman B
Light inducible dimers are powerful tools for cellular optogenetics as they can be used to control the localization and activity of proteins with high spatial and temporal resolution. Despite the generality of the approach, application of light inducible dimers is not always straightforward as it is frequently necessary to test alternative dimer systems and fusion strategies before the desired biological activity is achieved. This process is further hindered by an incomplete understanding of the biophysical/biochemical mechanisms by which available dimers behave and how this correlates to in vivo function. To better inform the engineering process we examined the biophysical and biochemical properties of three blue-light inducible dimer variants (Cryptochrome2 (CRY2)/CIB1, iLID/SspB, and LOVpep/ePDZ) and correlated these characteristics to in vivo co-localization and functional assays. We find that the switches vary dramatically in their dark-state and lit-state binding affinities, and that these affinities correlate with activity changes in a variety of in vivo assays including transcription control, intra-cellular localization studies and control of GTPase signaling. Additionally, for CRY2 we observe that light induced changes in homo-oligomerization can have large effects on activity that are sensitive to alternative fusion strategies.