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Tracking low-copy transcription factors in living bacteria: the case of the lac repressor

Abstract:
Transcription factors control the expression of genes by binding to specific sites in DNA and repressing or activating transcription in response to stimuli. The lac repressor (LacI) is a well characterized transcription factor that regulates the ability of bacterial cells to uptake and metabolize lactose. Here, we study the intracellular mobility and spatial distribution of LacI in live bacteria using photoactivated localization microscopy combined with single-particle tracking. Since we track single LacI molecules in live cells by stochastically photoactivating and observing fluorescent proteins individually, there are no limitations on the copy number of the protein under study; as a result, we were able to study the behavior of LacI in bacterial strains containing the natural copy numbers (∼40 monomers), as well as in strains with much higher copy numbers due to LacI overexpression. Our results allowed us to determine the relative abundance of specific, near-specific, and non-specific DNA binding modes of LacI in vivo, showing that all these modes are operational inside living cells. Further, we examined the spatial distribution of LacI in live cells, confirming its specific binding to lac operator regions on the chromosome; we also showed that mobile LacI molecules explore the bacterial nucleoid in a way similar to exploration by other DNA-binding proteins. Our work also provides an example of applying tracking photoactivated localization microscopy to studies of low-copy-number proteins in living bacteria.
Publication status:
Published
Peer review status:
Peer reviewed

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Role:
Author
ORCID:
0000-0001-5685-0352
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Institution:
University of Oxford
Division:
MPLS
Department:
Physics
Sub department:
Condensed Matter Physics
Oxford college:
St Cross College
Role:
Author



Publisher:
Cell Press
Journal:
Biophysical Journal More from this journal
Volume:
112
Issue:
7
Pages:
1316-1327
Publication date:
2017-04-11
Acceptance date:
2017-02-16
DOI:
EISSN:
1542-0086
ISSN:
0006-3495
Pmid:
28402875


Language:
English
Pubs id:
pubs:691145
UUID:
uuid:eb971c5b-d2ef-4f73-b5e5-d7488d839f31
Local pid:
pubs:691145
Deposit date:
2018-02-27

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