New alternately colored FRET sensors for simultaneous monitoring of Zn²⁺ in multiple cellular locations

• Published in: PloS one Vol. 7; no. 11; p. e49371
• Main Authors: Miranda, Jose G, Weaver, Amanda L, Qin, Yan, Park, J Genevieve, Stoddard, Caitlin I, Lin, Michael Z, Palmer, Amy E
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 16.11.2012; Public Library of Science (PLoS)
• Subjects: Active Transport, Cell Nucleus; Amino Acid Sequence; Biochemistry; Biology; Biosensing Techniques - methods; Biosensors; Cell Nucleus - metabolism; Cells (biology); Chemistry; Clover; Coding; Color; Compartments; Cytosol; Energy transfer; Engineering; Fluorescence; Fluorescence resonance energy transfer; Fluorescence Resonance Energy Transfer - methods; Genetic code; Genetic engineering; Golgi apparatus; Green Fluorescent Proteins - chemistry; Green Fluorescent Proteins - genetics; Green Fluorescent Proteins - metabolism; HeLa Cells; Humans; Kinases; Localization; Mitochondria; Monitoring; Motility; Nuclear reactions; Nuclei; Nuclei (cytology); Physics; Proteins; Rodents; Sensors; Sperm; Temporal resolution; Time Factors; Zinc; Zinc - metabolism; United States > US; Colorado
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0049371

Genetically encoded sensors based on fluorescence resonance energy transfer (FRET) are powerful tools for reporting on ions, molecules and biochemical reactions in living cells. Here we describe the development of new sensors for Zn²⁺based on alternate FRET-pairs that do not involve the traditional CFP and YFP. Zn²⁺ is an essential micronutrient and plays fundamental roles in cell biology. Consequently there is a pressing need for robust sensors to monitor Zn²⁺ levels and dynamics in cells with high spatial and temporal resolution. Here we develop a suite of sensors using alternate FRET pairs, including tSapphire/TagRFP, tSapphire/mKO, Clover/mRuby2, mOrange2/mCherry, and mOrange2/mKATE. These sensors were targeted to both the nucleus and cytosol and characterized and validated in living cells. Sensors based on the new FRET pair Clover/mRuby2 displayed a higher dynamic range and better signal-to-noise ratio than the remaining sensors tested and were optimal for monitoring changes in cytosolic and nuclear Zn²⁺. Using a green-red sensor targeted to the nucleus and cyan-yellow sensor targeted to either the ER, Golgi, or mitochondria, we were able to monitor Zn²⁺ uptake simultaneously in two compartments, revealing that nuclear Zn²⁺ rises quickly, whereas the ER, Golgi, and mitochondria all sequester Zn²⁺ more slowly and with a delay of 600-700 sec. Lastly, these studies provide the first glimpse of nuclear Zn²⁺ and reveal that nuclear Zn²⁺ is buffered at a higher level than cytosolic Zn²⁺.