The κ-opioid receptor (KOP) mediates the actions of opioids with hallucinogenic, dysphoric, and analgesic activities. The design of KOP analgesics devoid of hallucinatory and dysphoric effects has been hindered by an incomplete structural and mechanistic understanding of KOP agonist actions. Here, we provide a crystal structure of human KOP in complex with the potent epoxymorphinan opioid agonist MP1104 and an active-state-stabilizing nanobody. Comparisons between inactive- and active-state opioid receptor structures reveal substantial conformational changes in the binding pocket and intracellular and extracellular regions. Extensive structural analysis and experimental validation illuminate key residues that propagate larger-scale structural rearrangements and transducer binding that, collectively, elucidate the structural determinants of KOP pharmacology, function, and biased signaling. These molecular insights promise to accelerate the structure-guided design of safer and more effective κ-opioid receptor therapeutics.
We report the discovery of a simple system through which variant pyrrolysyl-tRNA synthetase/tRNACUAPyl pairs created in Escherichia coli can be used to expand the genetic code of Saccharomyces cerevisiae. In the process we have solved the key challenges of producing a functional tRNACUAPyl in yeast and discovered a pyrrolysyl-tRNA synthetase/tRNACUAPyl pair that is orthogonal in yeast. Using our approach we have incorporated an alkyne-containing amino acid for click chemistry, an important post-translationally modified amino acid and one of its analogs, a photocaged amino acid and a photo-cross-linking amino acid into proteins in yeast. Extensions of our approach will allow the growing list of useful amino acids that have been incorporated in E. coli with variant pyrrolysyl-tRNA synthetase/tRNACUAPyl pairs to be site-specifically incorporated into proteins in yeast.
The site-specific
incorporation of three new coumarin lysine analogues
into proteins was achieved in bacterial and mammalian cells using
an engineered pyrrolysyl-tRNA synthetase system. The genetically encoded
coumarin lysines were successfully applied as fluorescent cellular
probes for protein localization and for the optical activation of
protein function. As a proof-of-principle, photoregulation of firefly
luciferase was achieved in live cells by caging a key lysine residue,
and excellent OFF to ON light-switching ratios were observed. Furthermore,
two-photon and single-photon optochemical control of EGFP maturation
was demonstrated, enabling the use of different, potentially orthogonal
excitation wavelengths (365, 405, and 760 nm) for the sequential activation
of protein function in live cells. These results demonstrate that
coumarin lysines are a new and valuable class of optical probes that
can be used for the investigation and regulation of protein structure,
dynamics, function, and localization in live cells. The small size
of coumarin, the site-specific incorporation, the application as both
a light-activated caging group and as a fluorescent probe, and the
broad range of excitation wavelengths are advantageous over other
genetically encoded photocontrol systems and provide a precise and
multifunctional tool for cellular biology.
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