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Small molecule sensors
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<h2 id="uses">Uses</h2> <p>Metal ions are essential to virtually all biological systems and hence studying their concentrations with effective probes is highly advantageous. Since metal ions are key to the causes of <a href="/facts/Cancer/PVW6n1D0">cancer</a>, <a href="/facts/Diabetes/2xeHXbsI">diabetes</a>, and other diseases, monitoring them with probes that can provide insight into their concentrations with spatial and temporal resolution is of great interest to the scientific community.<a class="footnote-ref" id="fnref:4" href="#fn:4"><sup>4</sup></a> There are many applications that one can envision for small molecule sensors. It has been shown that one can use them to differentiate effectively between acceptable and harmful concentrations of <a href="/facts/Mercury_in_fish/zQVsWBnC">mercury in fish</a>.<a class="footnote-ref" id="fnref:5" href="#fn:5"><sup>5</sup></a> Further, since some types of <a href="/facts/Neurons/G7CyTVdH">neurons</a> uptake zinc during their operation, these probes can be used as a way to track activity in the brain and could serve as an effective alternative to <a href="/facts/Functional_MRI/GIayRTAL">functional MRI</a>.<a class="footnote-ref" id="fnref:6" href="#fn:6"><sup>6</sup></a> One can also track and quantify the growth of a <a href="/facts/Cell_(biology)/bLM9UQvy">cell</a>, such as a <a href="/facts/Fibroblast/n08KsFll">fibroblast</a>, that uptakes metal ions as it constructs itself.<a class="footnote-ref" id="fnref:7" href="#fn:7"><sup>7</sup></a> Numerous other biological processes can be tracked using small molecule sensors as many change metal concentrations as they occur, which can then be monitored. Still, the sensor must be tailored for its specific environment and sensing requirements. Depending on the application, the metal sensor should be selective for a certain type of metal, and especially needs to be able to bind its target metal with greater affinity than metals that naturally exist at high concentrations within the cell . Further, they should provide a response with a strong modulation in fluorescent spectrum and hence provide a high <a href="/facts/Signal-to-noise_ratio/qohClhyG">signal-to-noise ratio</a>. Finally, it is essential that a sensor is not toxic to the biological system in which it is used.<a class="footnote-ref" id="fnref:8" href="#fn:8"><sup>8</sup></a> </p> <h2 id="mechanisms-of-detection">Mechanisms of detection</h2> <p>Most detection mechanisms involved in small molecule sensors comprise some modulation in the fluorescent behavior of the sensing molecule upon binding the target metal. When a metal coordinates to such a sensor, it may either enhance or reduce the original fluorescent emission. The former is known as the Chelation Enhancement Fluorescence effect (CHEF), while the latter is called the Chelation Enhancement Quenching effect (CHEQ). By changing the intensity of emission at different wavelengths, the resulting fluorescent spectrum may attenuate, amplify, or shift upon the binding and dissociation of a metal. This shift in spectra can be monitored using a detector such as a microscope or a photodiode.<a class="footnote-ref" id="fnref:9" href="#fn:9"><sup>9</sup></a><a class="footnote-ref" id="fnref:10" href="#fn:10"><sup>10</sup></a> Listed below are some examples of mechanisms by which emission is modulated. Their participation in CHEQ or CHEF is dependent on the metal and small molecule sensor in question. </p> <h3>Primary Mechanisms of Detection</h3> <ul><li>Paramagnetic Fluorescence Quenching, the allowance of new electronic states upon binding a <a href="/facts/Paramagnetic/vj1SMbbp">paramagnetic</a> metal atom<a class="footnote-ref" id="fnref:11" href="#fn:11"><sup>11</sup></a></li> <li><a href="/facts/Photoinduced_electron_transfer/5p4Jb7uK">Photoinduced Electron Transfer (PET)</a>, the blocking of a lower <a href="/facts/Energy_state/66x51Khc">energy state</a> due to the binding of a metal atom.<a class="footnote-ref" id="fnref:12" href="#fn:12"><sup>12</sup></a></li> <li>Photoinduced Charge Transfer (PCT), the modulation of energy levels in a complex by charge transfer within a <a href="/facts/Conjugated_system/Ddx9qzox">conjugated pi system</a>.<a class="footnote-ref" id="fnref:13" href="#fn:13"><sup>13</sup></a></li> <li><a href="http://chemwiki.ucdavis.edu/Theoretical_Chemistry/Fundamentals/Fluorescence_Resonance_Energy_Transfer">Fluorescence Resonance Energy Transfer (FRET)</a>,<a class="footnote-ref" id="fnref:14" href="#fn:14"><sup>14</sup></a> the transfer of an <a href="/facts/Exciton/aFIBtIqQ">exciton</a> from a donor to an acceptor, modulating the emission spectrum.<a class="footnote-ref" id="fnref:15" href="#fn:15"><sup>15</sup></a><a class="footnote-ref" id="fnref:16" href="#fn:16"><sup>16</sup></a></li> <li><a href="/facts/Excimer/u5gfyLUI">Excimer/Exciplex formation</a>, the formation of a state that is a hybrid of the ground and excited states. This has novel fluorescent properties.<a class="footnote-ref" id="fnref:17" href="#fn:17"><sup>17</sup></a></li> <li>Chemodosimeters, complexes that undergo irreversible reactions with other species upon binding a metal to form new compounds with novel fluorescent spectra.<a class="footnote-ref" id="fnref:18" href="#fn:18"><sup>18</sup></a></li></ul> <h2 id="fluorophores">Fluorophores</h2> <p><a href="/facts/Fluorophores/wDWBmYhn">Fluorophores</a> are essential to our measurement of the metal binding event, and indirectly, metal concentration. There are many types, all with different properties that make them advantageous for different applications. Some work as small metal sensors completely on their own while others must be complexed with a subunit that can <a href="/facts/Chelate/4G79sXBB">chelate</a> or bind a metal ion. <a href="/facts/Rhodamine/M0IotHXt">Rhodamine</a> for example undergoes a <a href="/facts/Conformational_isomerism/JflrT5Ws">conformation</a> change upon the binding of a metal ion. In so doing it switches between a colorless, non-fluorescent <a href="/facts/Spirocyclic/XHxplGce">spirocyclic</a> form to a fluorescent, pink open cyclic form.<a class="footnote-ref" id="fnref:19" href="#fn:19"><sup>19</sup></a>[8] <a href="/facts/Quinoline/kJyUItFu">Quinoline</a> based sensors have been developed that form <a href="/facts/Luminescent/1QkIWyUj">luminescent</a> complexes with Cd(II) and fluorescent ones with Zn(II). It is hypothesized to function by changing its lowest luminescent state from n–π* to π–π* when coordinating to a metal.<a class="footnote-ref" id="fnref:20" href="#fn:20"><sup>20</sup></a><a class="footnote-ref" id="fnref:21" href="#fn:21"><sup>21</sup></a><a class="footnote-ref" id="fnref:22" href="#fn:22"><sup>22</sup></a> When the Dansyl group DNS binds to a metal, it loses a <a href="/facts/Sulfonamide/h1sVXW41">sulfonamide</a> hydrogen, causing fluorescence quenching via a PET or reverse PET mechanism in which an electron is transferred either to or from the metal that is bound.<a class="footnote-ref" id="fnref:23" href="#fn:23"><sup>23</sup></a> </p> <h2 id="examples">Examples</h2> <h3>Zinc</h3> <p><a href="/facts/Zinc/80b1qgk3">Zinc</a> is one of the most common metal ions in biological systems.<a class="footnote-ref" id="fnref:24" href="#fn:24"><sup>24</sup></a> Small molecule sensors for it include: </p> <ul><li>ZX1, a compound comprizing a dipicolylamine (DPA) Zinc binding subunit that has greater affinity for Zinc than other species found in solution such as Ca and Mg.<a class="footnote-ref" id="fnref:25" href="#fn:25"><sup>25</sup></a></li> <li>Zinpyr-1 (ZP1), a compound containing a <a href="/facts/Dichlorofluorescein/jbXf8g3F">dichlorofluorescein</a> fluorescent compound bound to two 2-picolamine (DPA) species that bind Zn(II). ZP1 is part of a family of zinc sensors known as the Zinpyr series, the members of which are variants on ZP1 to enable specific affinities and fluorescence profiles.<a class="footnote-ref" id="fnref:26" href="#fn:26"><sup>26</sup></a></li> <li>ZnAF-1 sensors that comprise an aryl donor and a xanthenone acceptor and have a large change in fluorescence upon binding Zn(II). They have been used to study uptake of Zn(II) in CA3 pyramidal neurons.<a class="footnote-ref" id="fnref:27" href="#fn:27"><sup>27</sup></a><a class="footnote-ref" id="fnref:28" href="#fn:28"><sup>28</sup></a></li> <li>GFZnP: A novel 12-member family of fluorescent GFP chemosensors was prepared for the detection of Zn2+ in biological samples with two-photon microscopy. These are the combination of the 8-aminoquinoline motif and the GFP chromophore unit, resulting enhanced fluorescent response to the Zn2+. The most effective members are GFZnP ED, GFZnP Pic and GFZnP dipic. GFZnPs have a simple synthesis and commercially available making them one of the most easily accessible two-photon Zn2+ sensors. The spectroscopical characterization of the probe family highlights their bright fluorescent emission (ε x Φ > 200) at λem= 520 nm upon excitation by λex= 450 nm light. The 2P-action cross section of the probes reaches δ´Φcomp > 5 GM at λex, 2P=900 nm, with an increase up to 200-fold, which makes them one of the best two-photon probes for Zn2+.Most of the members of the sensor family, especially GFZnP ED, GFZnP Pic and GFZnP dipic, exhibit high selectivity for Zn2+ with an affinity in the nanomolar (nM) range, excellent water-solubility, and usability at a wide pH-range (pH > 6). The applicability of selected probes was demonstrated by epifluorescent and 2P microscopy on cultured cells and brain slices. This work expands the toolbox of efficient two-photon zinc sensors with a valuable new family. [13]</li> <li>GFZnP OMe: An alternate, GFP-based fluorescent Zn2+ sensor is published for two-photon microscopy and related biological and microscop application. It composed of an 8-methoxyquinoline scaffold. It has excellent photophysical characteristics including a 37-fold fluorescence enhancement with l(ex) = 440 nm and l(em) = 505 nm. The two-photon cross-section is as high as 73 GM at 880 nm. [14]</li> <li>GFZnP BIPY: A Zn2+ selective fluorescent chemosensor with a 2,2’-bipyridine chelator moiety. It was effective at physiologically relevant pH-range and excellent photophysical characteristics are reported, including a 53-fold fluorescence enhancement with excitation and emission maxima at 422 nm and 492 nm, respectively. High two-photon cross-section of 3.0 GM at 840 nm as well as excellent metal ion selectivity are reported. In vitro experiments on HEK 293 cell culture were carried out using two-photon microscopy demonstrating the applicability. [15]</li></ul> <h3>Copper</h3> <p><a href="/facts/Copper/I8PEE8oX">Copper</a> is a biologically important metal to detect. It has many sensors developed for it including: </p> <ul><li>CTAP-1, a sensor that shows a response in the UV region when Cu(I) binds to an azatetrathiacrown motif that in turn excites a <a href="/facts/Pyrazoline/Cug43DfY">pyrazoline</a>-based dye that is attached. To use the probe, one excites it at 365 nm. If it is bound to Cu, then it will increase its fluorescence intensity. CTAP-1 is effective as it has a large modulation in its spectrum upon binding Cu, and is selective for the binding of Cu over other metals.<a class="footnote-ref" id="fnref:29" href="#fn:29"><sup>29</sup></a><a class="footnote-ref" id="fnref:30" href="#fn:30"><sup>30</sup></a></li> <li>Coppersensor-1 (CS1) that comprises a <a href="/facts/Thioether/GdyEz43f">thioether</a> rich motif that binds to Cu(I) causing the excitation of a boron-dipyrromethene (<a href="/facts/BODIPY/SGad9xI1">BODIPY</a>) dye in the visible region. The probe has good selectivity for Cu(I) over <a href="/facts/Alkaline_earth_metals/Ts4U5zIe">alkaline earth metals</a>, Cu(II), and <a href="/facts/D-block/BbzD5jUU">d-block metals</a>.<a class="footnote-ref" id="fnref:31" href="#fn:31"><sup>31</sup></a><a class="footnote-ref" id="fnref:32" href="#fn:32"><sup>32</sup></a></li></ul> <h3>Iron</h3> <p><a href="/facts/Iron/QK1JYy8E">Iron</a> is used a great deal in biological systems, a fact that is well known due to its role in <a href="/facts/Hemoglobin/RsD1MzYA">Hemoglobin</a>. For it, there are many small molecule sensors including: </p> <ul><li>Pryrene-TEMPO, in which the binding of iron to <a href="/facts/TEMPO/06hWvKMc">TEMPO</a> quenches the fluorescence of pyrene when no Fe(II) is bound. Upon binding however, TEMPO is reduced and <a href="/facts/Pyrene/BubR2koF">pyrene</a> regains fluorescence. This probe is limited in that an analogous response can be generated by unwanted <a href="/facts/Free_radicals/qFymuVoT">free radicals</a>, and that it can only by used in acidic solution.<a class="footnote-ref" id="fnref:33" href="#fn:33"><sup>33</sup></a><a class="footnote-ref" id="fnref:34" href="#fn:34"><sup>34</sup></a></li> <li>DansSQ, in which Fe(II) binding increases fluorescence at 460 nm. It consists of a Dansyl group bound to styrylquinoline and operates by the disruption of intra-molecular charge transfer upon the binding of Fe(II). It is limited in that it is only soluble in <a href="/facts/Acetonitrile/fNpbvRp6">acetonitrile</a> in 10% H2O.<a class="footnote-ref" id="fnref:35" href="#fn:35"><sup>35</sup></a></li></ul> <h3>Cobalt</h3> <p><a href="/facts/Cobalt/gqhScEw4">Cobalt</a> sensors have been made that capitalize on the breaking of C-O bonds by Co(II) in a fluorescent probe known as Cobalt Probe 1 (CP1).<a class="footnote-ref" id="fnref:36" href="#fn:36"><sup>36</sup></a> </p> <h3>Mercury</h3> <p><a href="/facts/Mercury_(element)/WlxfoHva">Mercury</a> is a toxic <a href="/facts/Heavy_metal_(chemistry)/Cblmy8qI">heavy metal</a>, and as such it is important to be able to detect it in biological systems. Sensors include: </p> <ul><li>Mercury Sensors (MS), a family of sensors that comprise complexes of fluorescein and napthofluorescein. The MS1 probe increases its emission upon binding of Hg(II), while maintaining great affinity for mercury over other heavy metal ions.<a class="footnote-ref" id="fnref:37" href="#fn:37"><sup>37</sup></a></li> <li>The S3 sensor is based on a <a href="/facts/BODIPY/SGad9xI1">BODIPY</a> complex which undergoes a significant increase in fluorescence upon the binding of Hg(II).<a class="footnote-ref" id="fnref:38" href="#fn:38"><sup>38</sup></a><a class="footnote-ref" id="fnref:39" href="#fn:39"><sup>39</sup></a></li> <li>MF1 uses a soft <a href="/facts/Thioether/GdyEz43f">thioether</a> chelator for Hg(II) bound to a fluorescein-like xanthenone reporter. It has good contrast upon binding mercury and good selectivity. MF1 is sensitive enough that it has been proposed to be used to test fish for toxic levels of mercury.<a class="footnote-ref" id="fnref:40" href="#fn:40"><sup>40</sup></a><a class="footnote-ref" id="fnref:41" href="#fn:41"><sup>41</sup></a></li></ul> <h2 id="see-also">See also</h2> <ul><li><a href="/facts/Chelation/4G79sXBB">Chelation</a></li> <li><a href="/facts/Luminescence/1QkIWyUj">Luminescence</a></li> <li><a href="/facts/Fluorescence/qsJVT2qP">Fluorescence</a></li> <li><a href="/facts/Fluorophore/wDWBmYhn">Fluorophore</a></li> <li><a href="/facts/Biosensor/MaUAS0gD">Biosensor</a></li> <li><a href="/facts/Deoxyribozyme/c7ApejX4">Deoxyribozyme</a></li></ul> <h2 id="references">References</h2> <ol> <li id="fn:1"><p>Tomat, Elisa; Lippard, Stephen J (April 2010). "Imaging mobile zinc in biology". Current Opinion in Chemical Biology. 14 (2): 225–230. doi:10.1016/j.cbpa.2009.12.010. PMC 2847655. PMID 20097117. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847655" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847655</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></p></li> <li id="fn:2"><p>Formica, Mauro; Fusi, Vieri; Giorgi, Luca; Micheloni, Mauro (January 2012). "New fluorescent chemosensors for metal ions in solution". Coordination Chemistry Reviews. 256 (1–2): 170–192. doi:10.1016/j.ccr.2011.09.010. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></p></li> <li id="fn:3"><p>Domaille, Dylan W; Que, Emily L; Chang, Christopher J (March 2008). "Synthetic fluorescent sensors for studying the cell biology of metals". Nature Chemical Biology. 4 (3): 168–175. doi:10.1038/nchembio.69. PMID 18277978. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:3" class="footnote-back-ref">↩</a></p></li> <li id="fn:4"><p>Domaille, Dylan W; Que, Emily L; Chang, Christopher J (March 2008). "Synthetic fluorescent sensors for studying the cell biology of metals". Nature Chemical Biology. 4 (3): 168–175. doi:10.1038/nchembio.69. PMID 18277978. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:4" class="footnote-back-ref">↩</a></p></li> <li id="fn:5"><p>Yoon, Sungho; Albers, Aaron E.; Wong, Audrey P.; Chang, Christopher J. (November 2005). "Screening Mercury Levels in Fish with a Selective Fluorescent Chemosensor". Journal of the American Chemical Society. 127 (46): 16030–16031. doi:10.1021/ja0557987. PMID 16287282. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:5" class="footnote-back-ref">↩</a></p></li> <li id="fn:6"><p>Hirano, Tomoya; Kikuchi, Kazuya; Urano, Yasuteru; Higuchi, Tsunehiko; Nagano, Tetsuo (December 2000). "Highly Zinc-Selective Fluorescent Sensor Molecules Suitable for Biological Applications". Journal of the American Chemical Society. 122 (49): 12399–12400. doi:10.1021/ja002467f. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:6" class="footnote-back-ref">↩</a></p></li> <li id="fn:7"><p>Domaille, Dylan W; Que, Emily L; Chang, Christopher J (March 2008). "Synthetic fluorescent sensors for studying the cell biology of metals". Nature Chemical Biology. 4 (3): 168–175. doi:10.1038/nchembio.69. PMID 18277978. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:7" class="footnote-back-ref">↩</a></p></li> <li id="fn:8"><p>Domaille, Dylan W; Que, Emily L; Chang, Christopher J (March 2008). "Synthetic fluorescent sensors for studying the cell biology of metals". Nature Chemical Biology. 4 (3): 168–175. doi:10.1038/nchembio.69. PMID 18277978. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:8" class="footnote-back-ref">↩</a></p></li> <li id="fn:9"><p>Formica, Mauro; Fusi, Vieri; Giorgi, Luca; Micheloni, Mauro (January 2012). "New fluorescent chemosensors for metal ions in solution". Coordination Chemistry Reviews. 256 (1–2): 170–192. doi:10.1016/j.ccr.2011.09.010. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:9" class="footnote-back-ref">↩</a></p></li> <li id="fn:10"><p>Carter, Kyle P.; Young, Alexandra M.; Palmer, Amy E. (23 April 2014). "Fluorescent Sensors for Measuring Metal Ions in Living Systems". Chemical Reviews. 114 (8): 4564–4601. doi:10.1021/cr400546e. PMC 4096685. PMID 24588137. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096685" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096685</a> <a href="#fnref:10" class="footnote-back-ref">↩</a></p></li> <li id="fn:11"><p>Formica, Mauro; Fusi, Vieri; Giorgi, Luca; Micheloni, Mauro (January 2012). "New fluorescent chemosensors for metal ions in solution". Coordination Chemistry Reviews. 256 (1–2): 170–192. doi:10.1016/j.ccr.2011.09.010. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:11" class="footnote-back-ref">↩</a></p></li> <li id="fn:12"><p>Formica, Mauro; Fusi, Vieri; Giorgi, Luca; Micheloni, Mauro (January 2012). "New fluorescent chemosensors for metal ions in solution". 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