DNA binding fluorescent proteins for the direct visualization of large DNA molecules
Author(s) -
Seonghyun Lee,
Yeeun Oh,
Jung-Yoon Lee,
Sojeong Choe,
Sangyong Lim,
Hyun Soo Lee,
Kyubong Jo,
David C. Schwartz
Publication year - 2015
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkv834
Subject(s) - dna , biology , fluorophore , fluorescence , dna binding protein , biochemistry , biophysics , protein–dna interaction , dna binding site , microbiology and biotechnology , gene , promoter , transcription factor , gene expression , physics , quantum mechanics
Fluorescent proteins that also bind DNA molecules are useful reagents for a broad range of biological applications because they can be optically localized and tracked within cells, or provide versatile labels for in vitro experiments. We report a novel design for a fluorescent, DNA-binding protein (FP-DBP) that completely ‘paints’ entire DNA molecules, whereby sequence-independent DNA binding is accomplished by linking a fluorescent protein to two small peptides (KWKWKKA) using lysine for binding to the DNA phosphates, and tryptophan for intercalating between DNA bases. Importantly, this ubiquitous binding motif enables fluorescent proteins ( K d = 14.7 μM) to confluently stain DNA molecules and such binding is reversible via pH shifts. These proteins offer useful robust advantages for single DNA molecule studies: lack of fluorophore mediated photocleavage and staining that does not perturb polymer contour lengths. Accordingly, we demonstrate confluent staining of naked DNA molecules presented within microfluidic devices, or localized within live bacterial cells.
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