A roadmap to success in photopharmacology.

Light is a fascinating phenomenon that ties together physics, chemistry, and biology. It is unmatched in its ability to confer information with temporal and spatial precision and has been used to map objects on the scale of tens of nanometers (10(-8) m) to light years (10(16) m). This information, gathered through super-resolution microscopes or space-based telescopes, is ultimately funneled through the human visual system, which is a miracle in itself. It allows us to see the Andromeda galaxy at night, an object that is 2.5 million light years away and very dim, and ski the next day in bright sunlight at an intensity that is 12 orders of magnitude higher. Human vision is only one of many photoreceptive systems that have evolved on earth and are found in all kingdoms of life. These systems rely on molecular photoswitches, such as retinal or tetrapyrrols, which undergo transient bond isomerizations or bond formations upon irradiation. The set of chromophores that have been employed in Nature for this purpose is surprisingly small. Nevertheless, they control a wide variety of biological functions, which have recently been significantly increased through the rapid development of optogenetics. Optogenetics originated as an effort to control neural function with genetically encoded photoreceptors that use abundant chromophores, in particular retinal. It now covers a variety of cellular functions other than excitability and has revolutionized the control of biological pathways in neuroscience and beyond. Chemistry has provided a large repertoire of synthetic photoswitches with highly tunable properties. Like their natural counterparts, these chromophores can be attached to proteins to effectively put them under optical control. This approach has enabled a new type of synthetic photobiology that has gone under various names to distinguish it from optogenetics. We now call it photopharmacology. Here we trace our involvement in this field, starting with the first light-sensitive potassium channel (SPARK) and concluding with our most recent work on photoswitchable fatty acids. Instead of simply providing a historical account of our efforts, we discuss the design criteria that guided our choice of molecules and receptors. As such, we hope to provide a roadmap to success in photopharmacology and make a case as to why synthetic photoswitches, properly designed and made available through well-planned and efficient syntheses, should have a bright future in biology and medicine.

[1]  D. Trauner,et al.  Photoswitchable fatty acids enable optical control of TRPV1 , 2015, Nature Communications.

[2]  A. Gottschalk,et al.  AzoCholine Enables Optical Control of Alpha 7 Nicotinic Acetylcholine Receptors in Neural Networks. , 2015, ACS chemical neuroscience.

[3]  G. Rutter,et al.  A red-shifted photochromic sulfonylurea for the remote control of pancreatic beta cell function. , 2015, Chemical communications.

[4]  Sarah J. Backe,et al.  The cis‐state of an azobenzene photoswitch is stabilized through specific interactions with a protein surface , 2015, Journal of molecular recognition : JMR.

[5]  Yigong Shi A Glimpse of Structural Biology through X-Ray Crystallography , 2014, Cell.

[6]  G. Rutter,et al.  Optical control of insulin release using a photoswitchable sulfonylurea , 2014, Nature Communications.

[7]  P. Gorostiza,et al.  An allosteric modulator to control endogenous G protein-coupled receptors with light. , 2014, Nature chemical biology.

[8]  P. Haycock,et al.  Arylazopyrazoles: azoheteroarene photoswitches offering quantitative isomerization and long thermal half-lives. , 2014, Journal of the American Chemical Society.

[9]  D. Trauner,et al.  Controlling epithelial sodium channels with light using photoswitchable amilorides. , 2014, Nature chemistry.

[10]  D. Trauner,et al.  Optical control of acetylcholinesterase with a tacrine switch. , 2014, Angewandte Chemie.

[11]  D. Trauner,et al.  Development of a new photochromic ion channel blocker via azologization of fomocaine. , 2014, ACS chemical neuroscience.

[12]  D. Trauner,et al.  Ligand Photo-Isomerization Triggers Conformational Changes in iGluR2 Ligand Binding Domain , 2014, PloS one.

[13]  D. Trauner,et al.  A photochromic agonist for μ-opioid receptors. , 2014, Angewandte Chemie.

[14]  Dirk Trauner,et al.  Restoring Visual Function to Blind Mice with a Photoswitch that Exploits Electrophysiological Remodeling of Retinal Ganglion Cells , 2014, Neuron.

[15]  Wiktor Szymanski,et al.  Photopharmacology: beyond proof of principle. , 2014, Journal of the American Chemical Society.

[16]  D. Trauner,et al.  A photoswitchable neurotransmitter analogue bound to its receptor. , 2013, Biochemistry.

[17]  Dirk Trauner,et al.  A red-shifted, fast-relaxing azobenzene photoswitch for visible light control of an ionotropic glutamate receptor. , 2013, Journal of the American Chemical Society.

[18]  B. Feringa,et al.  Optical control of antibacterial activity. , 2013, Nature chemistry.

[19]  K. Deisseroth,et al.  Optogenetics , 2013, Proceedings of the National Academy of Sciences.

[20]  T. Gudermann,et al.  Optical control of TRPV1 channels. , 2013, Angewandte Chemie.

[21]  H. Adesnik,et al.  Optogenetic pharmacology for control of native neuronal signaling proteins , 2013, Nature Neuroscience.

[22]  A. Schier,et al.  Optical Control of Metabotropic Glutamate Receptors , 2013, Nature Neuroscience.

[23]  R. Kramer,et al.  Light at the end of the channel: optical manipulation of intrinsic neuronal excitability with chemical photoswitches , 2013, Front. Mol. Neurosci..

[24]  S. Hecht,et al.  o-Fluoroazobenzenes as readily synthesized photoswitches offering nearly quantitative two-way isomerization with visible light. , 2012, Journal of the American Chemical Society.

[25]  D. Raines,et al.  Azo-propofols: photochromic potentiators of GABA(A) receptors. , 2012, Angewandte Chemie.

[26]  Dirk Trauner,et al.  Photochemical Restoration of Visual Responses in Blind Mice , 2012, Neuron.

[27]  D. Trauner,et al.  A photochromic agonist of AMPA receptors. , 2012, Angewandte Chemie.

[28]  Dirk Trauner,et al.  Optochemical control of genetically engineered neuronal nicotinic acetylcholine receptors. , 2012, Nature chemistry.

[29]  Dirk Trauner,et al.  Tuning photochromic ion channel blockers. , 2011, ACS chemical neuroscience.

[30]  Estíbaliz Merino,et al.  Synthesis of azobenzenes: the coloured pieces of molecular materials. , 2011, Chemical Society reviews.

[31]  J. Baell,et al.  New substructure filters for removal of pan assay interference compounds (PAINS) from screening libraries and for their exclusion in bioassays. , 2010, Journal of medicinal chemistry.

[32]  Dirk Trauner,et al.  Photochromic blockers of voltage-gated potassium channels. , 2009, Angewandte Chemie.

[33]  E. Isacoff,et al.  Nanosculpting reversed wavelength sensitivity into a photoswitchable iGluR , 2009, Neuroscience Research.

[34]  Timothy W. Dunn,et al.  Photochemical control of endogenous ion channels and cellular excitability , 2008, Nature Methods.

[35]  E. Isacoff,et al.  Reversibly caged glutamate: a photochromic agonist of ionotropic glutamate receptors. , 2007, Journal of the American Chemical Society.

[36]  E. Isacoff,et al.  Light-activated ion channels for remote control of neuronal firing , 2004, Nature Neuroscience.

[37]  Carole Williams,et al.  Tethered blockers as molecular ‘tape measures’ for a voltage-gated K+ channel , 2000, Nature Structural Biology.

[38]  B. Chait,et al.  The structure of the potassium channel: molecular basis of K+ conduction and selectivity. , 1998, Science.

[39]  E. Eyring,et al.  Kinetics of acid dissociation-ion recombination of aqueous methyl orange , 1972 .

[40]  G. Hartley,et al.  The Cis-form of Azobenzene , 1937, Nature.

[41]  D. Trauner,et al.  Optochemical genetics. , 2011, Angewandte Chemie.

[42]  E. Isacoff,et al.  Allosteric control of an ionotropic glutamate receptor with an optical switch , 2006, Nature chemical biology.