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Characterization of an Enantioselective Odorant Receptor in the Yellow Fever Mosquito Aedes aegypti

  • Jonathan D. Bohbot,

    Affiliation United States Department of Agriculture, Agricultural Research Service, Henry A. Wallace Beltsville Agricultural Research Center, Plant Sciences Institute, Invasive Insect Biocontrol and Behavior Laboratory, Beltsville, Maryland, United States of America

  • Joseph C. Dickens

    joseph.dickens@ars.usda.gov

    Affiliation United States Department of Agriculture, Agricultural Research Service, Henry A. Wallace Beltsville Agricultural Research Center, Plant Sciences Institute, Invasive Insect Biocontrol and Behavior Laboratory, Beltsville, Maryland, United States of America

Abstract

Enantiomers differ only in the left or right handedness (chirality) of their orientations and exhibit identical chemical and physical properties. In chemical communication systems, enantiomers can be differentially active at the physiological and behavioral levels. Only recently were enantioselective odorant receptors demonstrated in mammals while their existence in insects has remained hypothetical. Using the two-microelectrode voltage clamp of Xenopus oocytes, we show that the yellow fever mosquito, Aedes aegypti, odorant receptor 8 (AaOR8) acts as a chiral selective receptor for the (R)-(—)-enantiomer of 1-octen-3-ol, which in the presence of other kairomones is an attractant used by blood-sucking insects to locate their hosts. In addition to steric constraints, chain length and degree of unsaturation play important roles in this recognition process. This is the first characterization of an enantioselective odorant receptor in insects and the results demonstrate that an OR alone, without helper proteins, can account for chiral specificity exhibited by olfactory sensory neurons (OSNs).

Introduction

Chiral specificity is certainly the most remarkable accomplishment of olfactory systems. From the elephant and beetle chiral pheromone frontalin [1] to the enantioselective abilities of squirrel monkeys [2], examples of chiral signals abound. Since the early 1970s, enantioselectivity of insect [3] olfactory systems has been well documented. Evidence ranges from enantiomer driven behaviors [4], [5], [6], [7], [8] and glomerular activation patterns [9] to highly specific olfactory receptor cells for pheromones and plant odorants [10], [11]. In fact, behavioral studies carried out in humans [2], honeybees [12] and mice [13] have clearly demonstrated the ability of these organisms to distinguish between chiral odorants, prompting several authors to postulate the existence of enantioselective ORs. Recently, one report has presented direct evidence that some mice ORs can discriminate odorant enantiomers [14]. As insect and vertebrate Or genes are phylogenetically unrelated [15], limited data exist at the molecular level for discrimination of enantiomers by insect ORs [16].

Insect OSNs typically express a combination of a member of the conventional OR family and a ubiquitously expressed and highly conserved co-receptor [17], [18], [19]. While the exact composition of this heteromeric complex remains unknown, it is apparent that the interaction between a variable odorant-binding OR and an obligatory partner protein called OR7 in mosquitoes [20], [21], [22], 83b in flies [17], and OR2 in bees [23] and moths [24], [25] is necessary to create a functional ion channel [26] and perhaps activate a G-protein pathway [27].

Racemic 1-octen-3-ol (CH3[CH2]4CH[OH]CH = CH2) is a mono-unsaturated 8-carbon alcohol with carbon 3 being the single stereogenic center (Fig. 1A), hence its composition of two optically active enantiomers, (R)-(—)-1-octen-3-ol and (S)-(+)-1-octen-3-ol. Octenol is a natural compound of plant [28] and animal origin [29], and has been identified from human sweat extracts [30]. (R)-(—)-1-octen-3-ol is the prevailing enantiomer in volatiles collected from cattle with a (R)/(S) ratio between 80% and 92% [29]. While both octenol enantiomers are equally active aggregation pheromones for several beetle species [31] and potent attractants to the tsetse fly, Glossina morsitans [29], many mosquito species exhibit a preference for the (R)-(—) form [32], [33]. This compound alone is an attractant for various hematophagous insects [29], [34] and its behavioral potency is increased when combined with CO2 [35]. OSNs located within the capitate peg sensilla on the maxillary palps of Aedes aegypti [36], Culex quinquefasciatus [33] and Anopheles gambiae [16] mediate the response to octenol and CO2. In the case of An. gambiae, the molecular basis of the octenol response has previously been attributed to An. gambiae OR8 (AgOR8) [16]. We recently identified the Or gene family of Ae. aegypti including the Ae. aegypti orthologue of AgOr8, AaOr8 [37]. In the current study, we establish that octenol is the preferred ligand of the AaOR8/AaOR7 protein complex, and investigate the structure-activity relationship between ligand and receptor, focusing on the enantiomeric discrimination of (R)- and (S)-octenol.

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Figure 1. AaOR8 discriminates between the two enantiomers of 1-octen-3-ol.

(A) The odorant 1-octen-3-ol occurs in two configurations: (R) and (S). Asterisk indicates the chiral center. (B) Response traces of AaOR8 to each enantiomer are recorded in nano-ampere (nA). For space considerations, time scales differ. (C) Concentration-response plots of AaOR8 to each enantiomer of 1-octen-3-ol (n = 6). Odorant concentrations were plotted on a logarithmic scale. Each point represents the mean and vertical current response; error bars are s.e.m. Responses to 10−5 M 1-octen-3-ol are highlighted in red.

https://doi.org/10.1371/journal.pone.0007032.g001

Results

AaOR8 is activated by (R)-(—)-1-octen-3-ol

Along with AaOr8, we co-expressed AaOr7 in Xenopus oocytes and electrophysiological responses (Fig. 1B) to each enantiomer were measured using the two-microelectrode voltage clamp technique. In contrast to AaOR8, which belongs to the highly divergent class of ORs, members of the insect OR7 family exhibit high sequence homology and associate with conventional ORs to form a functional hetero-complex [15]. We established the concentration-response relationships for each compound (Fig. 1C) and their associated half maximal effective concentration (EC50) as a sensitivity criterion. AaOR8 was most sensitive to the (R)-(—)-1-octen-3-ol with an EC50 value of 158 nM, two orders of magnitude lower than to the (S)-(+)-enantiomer (EC50 = 17,200 nM). Part of the response to the (S)-(+)-enantiomer may have been caused by the presence of trace amounts (1 part per thousand) of the (R)-(—)-enantiomer (see Material & Methods).

Effect of the chiral center on AaOR8 activation

Deduced EC50 ranking agonist profiles were used to further evaluate the importance of the chiral center in this recognition process (Figs. 2 and 3). Replacing the hydroxy moiety of octenol by a ketone group, rendering the molecule achiral, reduced AaOR8 sensitivity by over two log steps (Fig. 2A and E). Displacing the chiral center to position C4 had a similar effect on AaOR8 sensitivity (Fig. 2B and E).

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Figure 2. Strong preference of AaOR8 towards (R)-(—)-1-octen-3-ol.

The concentration-response plot for (R)-(—)-1-octen-3-ol was repeated in each panel for comparative purposes. (A) Importance of C3 as a chiral center. Concentration-response plots of AaOR8 to 1-octen-3-one (n = 6). (B) Shifting the chiral center from C3 to C4 reduces AaOR8 sensitivity. Concentration-response plots of AaOR8 to 1-octen-4-ol (n = 8). (C) Side chain length affects AaOR8 sensitivity. Concentration-response plots of AaOR8 to 1-nonen-3-ol and 1-hepten-3-ol (n = 8 to 9). (D) The double bond is critical for recognition by AaOR8. Concentration-response plots of AaOR8 to 3-octanol (n = 6). (E) EC50 ranking profile of AaOR8 for octenol related compounds. Asterisk, p<0.05; two asterisks, p<0.01 and three asterisks, p<0.001. Odorant concentrations were plotted on a logarithmic scale. Each point represents the mean and error bars indicate s.e.m.

https://doi.org/10.1371/journal.pone.0007032.g002

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Figure 3. Relative activity of AaOR8 towards (R)-(—)-1-octen-3-ol and related compounds.

Changes relative to (R)-(—)-1-octen-3-ol are shaded in grey. Presence and absence of a specific chemical feature are indicated by + and -, respectively. The formula of racemic compounds does not assume the 3 dimensional orientation of the residues attached to the chiral center. Note that the least active isomers are those lacking the proper chirality at the 3-position (C3*). Relative activities of each odorant (EC50s) are reflected by area of solid circles.

https://doi.org/10.1371/journal.pone.0007032.g003

Chain length and unsaturation are required for AaOR8 activation

Chain length and degree of unsaturation also proved to be important determinants for AaOR8 sensitivity (Fig. 2, C and D). Adding or removing one carbon lowered the response of AaOR8, although in an asymmetric fashion. AaOR8 displayed higher sensitivity to the longer C9 alcohol, 1-nonen-3-ol, than to the shorter C7 alcohol, 1-hepten-3-ol (Fig. 2, C and E). Lower sensitivity to 1-hepten-3-ol had already been shown in the case of AgOR8 [16]. Unsaturation on carbon 1 was of consequence as the saturated 3-octanol compound decreased AaOR8 sensitivity 10-fold compared to (R)-(—)-1-octen-3-ol (Fig. 2D and E), a result consistent with previously reported electrophysiological data [33]. This latter observation implies that the steric arrangement and size of the groups attached to the chiral center might be more important in overall activity of the molecule than the carbon double bond (Fig. 2E and 3), since (R)-3-octanol comprised half of this racemic blend. In fact, the most effective compounds in our study had a chiral center at the 3-position (Fig. 3).

Discussion

Here we show for the first time conclusive evidence that an insect OR is capable of enantioselectivity. However, other types of isomer selectivity by ORs have previously been reported. An. gambiae ORs exhibit preferences for positional isomers of cresol [38] and a larval OR from Bombyx mori discriminates between cis/trans isomers of jasmone [39]. Electrophysiological studies have shown that receptor neurons can respond selectively to enantiomers. For example, the Japanese beetles, Anomala osakana and Popillia japonica, respond to both enantiomers of the japonilure pheromone with opposite behavioral effects [5]. This behavior is mediated by two different OSNs, localized within the same sensillum, that respond specifically to one enantiomer [40]. It was also shown that pheromone-binding protein (PBP) did not discriminate between the two enantiomers [40]. Similar evidence was advanced in the case of Cx. quinquefasciatus in which OSN B in the capitate pegs displayed strong selectivity for (R)-(—)-1-octen-3-ol [33].

Lu et al. [16] showed that AgOR8, when expressed in oocytes, was narrowly tuned and responded best to the racemic 1-octen-3-ol among a panel of 82 odorants. Their study indicated the possibility that AgOR8 was capable of enantioselectivity. However, this property was not conclusively demonstrated due to the absence of dose-response curves for the (R) and (S) forms of 1-octen-3-ol. OSN B in the capitate peg sensillum of An. gambiae responds to racemic 1-octen-3-ol and the same neuron in Cx. quinquefasciatus discriminates both enantiomers [33]. The presence of the Or8 gene in both An. gambiae and Ae. aegypti genomes [37], [41], two species separated by 140-200 million years [42], and the fact that Cx. quinquefasciatus is able to discriminate both octenol enantiomers at the physiological level, strongly suggest that the molecular detection mechanism for this kairomone has been conserved in the Culicinae lineage. It remains to test this hypothesis with AgOR8 and the Cx. quinquesfasciatus counterpart.

AaOR8 displays sensitivity levels akin to the ones observed between insect pheromone receptors expressed in Xenopus oocytes and their cognate pheromone ligands [24], [43]. The honey bee Apis mellifera OR11 (AmOR11) responds to the queen pheromone 9-oxo-2-decenoic acid at the nanomolar range while other AmORs exhibit weak or no response to the same compound [43]. In contrast, Bombyx mori OR1 (BmOR1) response to bombykol in the oocyte expression system is in the micromolar range [24].

The most important conclusion from these experiments is that the chiral center is critical for proper recognition of (R)-(—)-1-octen-3-ol by AaOR8. AaOR8 exhibits a strong preference towards (R)-(—)-1-octen-3-ol and an exquisite degree of selectivity between the two enantiomeric forms, compatible with the notion that the topography of the prospective binding site is complementary to that of (R)-(—)-1-octen-3-ol in order to maximize the desired interactions. Chain length and the steric arrangement provided by the chiral center are critical for AaOR8 activation. The differential selectivity of AaOR8 towards both enantiomers of octenol and the loss of sensitivity toward the planar conjugated ketone suggest that one likely interaction involves a hydrogen bond between the oxygen atom of the hydoxyl moiety attached to the chiral center and an amino-acid residue in the receptor binding pocket. Whether the oxygen atom is a hydrogen bond donor or acceptor will have to be determined experimentally.

Our experiments suggest that ORs with “broad” response spectra [44] may actually be narrowly tuned to cognate ligands yet to be discovered and underscore the necessity to test individual enantiomers when chiral odorants are involved. New families of olfactory receptors identified in vertebrates [45] and insects [46] expand the response repertoire for specific ligands whose detection heretofore was assigned to broadly tuned ORs. Moreover, AaOR8 enantioselectivity advocates the shape theory of olfaction over vibrational theories since both octenol enantiomers have identical vibrational signatures but different shapes [47].

While several reports have shown that odorant-binding proteins (OBPs) present in the perireceptor lymph enhance OSN sensitivity [48], [49] and in a few cases participate in odorant specificity [50], most ORs can be activated by odorants directly [51], [52]. DMSO, the organic solvent used in our experiments, has been shown to be as efficient as pheromone-binding proteins (PBPs) at sensitizing OSNs to odorants [49]. As such, DMSO is certainly responsible for the overall activation of these receptors by serving as a carrier thus presenting the tested odorants to them. The dose-response relationships describing the various degrees of sensitivity between AaOR8 and closely related octenol analogues range between 10 and 100-fold. As a constant parameter, the organic solvent DMSO cannot be responsible for the differential sensitivity levels of AaOR8 and notably for its remarkable enantioselective capabilities. Therefore, we propose that part of the sensitivity and most of the specificity toward (R)-(—)-1-octen-3-ol is achieved by AaOR8 and these features may not require the assistance of helper proteins such as the OBPs present in the perireceptor lymph. These findings do not necessarily exclude the possibility that OBPs, thought to ferry odorants to the ORs, may be involved in the sensitivity and specificity of the 1-octen-3-ol sensing OSNs.

However, evidence supporting the potential enantioselective properties of OBPs in insects is scant. For example, pheromone receptor neurons of the gypsy moth, Lymantria dispar, well discriminate the two enantiomers of the pheromone disparlure [53]. Plettner et al. showed that PBP1 and PBP2 differentiate [54], albeit slightly [55], the two enantiomers of the pheromone. This selectivity was not observed in an earlier study [56]. In fact, a crystallographic study in cockroach indicates that PBP does not discriminate the two enantiomeric pairs of the cockroach pheromone [57]. Our cell expression assay being devoid of OBPs suggests that AaOR8 is sufficient to account for enantioselectivity and is consistent with electrophysiological data gathered from the mosquito Cx. quinquefasciatus [33]. These results represent an important step toward understanding enantioselectivity in odorant detection processes. Further, a basis is provided for the utilization of ORs for the discovery of behaviorally and optically active drugs in the same fashion the pharmaceutical field has done for the past 30 years.

Materials and Methods

Heterologous Expression of AaOr7 and AaOr8 in Xenopus laevis Oocytes

AaOr7 and AaOr8 cRNAs were synthesized from linearized pSP64DV expression vectors (Dr. Zwiebel, Vanderbilt University) using the mMESSAGE mMACHINE SP6 kit (Ambion). Following mechanical disruption of the Xenopus ovaries, stage V-VII oocytes were treated for 30 min at room temperature under 150 rpm shaking with a 2 mg/mL collagenase (SIGMA, C6895) solution in OR-2 buffer (5 mM HEPES, 1 mM Na2HPO4, 82.5 mM NaCl, and 2.5 mM MgCl2 [pH 7.6]). All procedures were performed in accordance with the NIH Institutional Animal Care and Use Committee and NIH guidelines. Oocytes were subsequently washed 5 times with OR-2 buffer, 5 times with MBSH buffer (10 mM HEPES, 2.4 mM NaHCO3, 8.8 mM NaCl, 1 mM KCl, 0.82 mM MgSO4, 0.41 mM CaCl2 and 0.33 mM (CaNO3)2, [pH 7.6]), 5 times with MBSH supplemented with 50 µg/ML gentamycin and 5 times with Ringer's buffer (96 mM NaCl, 2 mM KCl, 5 mM MgCl2, 6H2O, 5 mM HEPES and 0.8 mM CaCl2 [pH 7.6]) supplemented with 5% heat-inactivated horse serum, 50 µg/mL tetracycline, 100 µg/mL streptomycin and 550 µg/mL sodium pyruvate. Individual oocytes were allowed to recover overnight prior to injection with 10 ng of each cRNA and were recorded 4 to 6 days post-injection.

Electrophysiological Recordings

Whole-cell currents were recorded using the two-microelectrode voltage clamp technique [24], [58]. Odorants were dissolved in dimethyl sulfoxide (DMSO) at a 1∶10 ratio so that stock solutions could be made. Prior to recording, stock solutions were diluted in Ringer's solution [pH 7.6] (96 mM NaCl, 2 mM KCl, 5 mM MgCl2, 5 mM HEPES and 0.8 mM CaCl2) to the indicated concentrations before being applied to Xenopus oocytes in a RC-3Z oocyte recording chamber (Warner Instruments). Oocytes were continuously perfused by either pure Ringer's solution or exposed for 8 sec to serial dilutions of odorants dissolved in Ringer's solution. Odorant-induced currents were recorded with an OC-725C oocyte clamp (Warner Instruments) at a holding potential of −80 mV. Between stimulations, oocytes were allowed to return to their membrane resting potential by washing out the odorants using pure Ringer's solution. Data acquisition and analysis were carried out with Digidata 1440A and pCLAMP10 software (Axon Instruments).

Data Analysis

Statistical analyses (GraphPad Prism5 Software, Inc.) of the logEC50 means were performed using an ordinary one-way ANOVA in conjunction with the Tukey Kramer multiple comparison post test (95% confidence interval). Multiple comparison tests reported by Prism5 do not report exact P values but tell the significance level for each pairwise comparison (see Fig. 2 legend). In all figures, graphical results are shown as means and standard error of the mean for a minimum of six independent oocytes. EC50 values for individual compounds were extrapolated using the non-linear regression curve fit function provided in Prism5.

Materials

3-Octanol (99%) and 1-hepten-3-ol (97%) were obtained from SIGMA. 1-Nonen-3-ol (98%), 1-octen-3-one (97%) and 1-octen-4-ol (99%) were obtained from Alfa Aesar. (R)-(—)-1-octen-3-ol (99.6% R) and (S)-(+)-1-octen-3-ol (99.9% S) were custom synthesized by Bedoukian Research, Inc.

Acknowledgments

We would like to acknowledge Dr. Laurence Zwiebel of Vanderbilt University for providing the AaOr8 and AaOr7 expression vectors. We thank Bedoukian Research, Inc., Danbury, Connecticut USA for the enantiomers of 1-octen-3-ol. We offer special thanks to Dr. Liezhen Fu and Dr. Yun-Bo Shi, National Institutes of Health, for graciously providing Xenopus oocytes.

Author Contributions

Conceived and designed the experiments: JDB JCD. Performed the experiments: JDB. Analyzed the data: JDB. Contributed reagents/materials/analysis tools: JDB JCD. Wrote the paper: JDB JCD.

References

  1. 1. Greenwood DR, Comeskey D, Hunt MB, Rasmussen LE (2005) Chemical communication: chirality in elephant pheromones. Nature 438: 1097–1098.
  2. 2. Laska M, Liesen A, Teubner P (1999) Enantioselectivity of odor perception in squirrel monkeys and humans. Am J Physiol 277: 1098–1003.
  3. 3. Iwaki S, Marumo S, Saito T, Yamada M, Katagiri K (1974) Synthesis and activity of optically active disparlure. J Am Chem Soc 96: 78442–77844.
  4. 4. Mori K (1998) Chiral insect pheromones. Chirality 10: 578–586.
  5. 5. Tumlinson JH, Klein MG, Doolittle RE, Ladd TL, Proveaux AT (1977) Identification of the female Japanese beetle sex pheromone: Inhibition of male response by an enantiomer. Science 197: 789–792.
  6. 6. Leal WS (1996) Chemical communication in scarab beetles: reciprocal behavioral agonist-antagonist activities of chiral pheromones. Proc Natl Acad Sci U S A 93: 12112–12115.
  7. 7. Bierl BA, Beroza M, Collier CW (1970) Potent sex attractant of the gypsy moth: its isolation, identification, and synthesis. Science 170: 87–89.
  8. 8. Zhang QH, Chauhan KR, Erbe EF, Vellore AR, Aldrich JR (2004) Semiochemistry of the goldeneyed lacewing Chrysopa oculata: attraction of males to a male-produced pheromone. J Chem Ecol 30: 1849–1870.
  9. 9. Reisenman CE, Christensen TA, Francke W, Hildebrand JG (2004) Enantioselectivity of projection neurons innervating identified olfactory glomeruli. J Neurosci 24: 2602–2611.
  10. 10. Dickens JC (1990) Specialized receptor neurons for pheromones and host plant odors in boll weevil, Anthonomus grandis Boh. (Coleoptera: Curculionidae). Chem Senses 15: 311–333.
  11. 11. Dickens JC (1978) Olfactory perception of pheromone and host odor enantiomers by Ips typographus L. (Coleoptera: Scolytidae). Entomol Exp et App 24: 136–142.
  12. 12. Laska M, Galizia CG (2001) Enantioselectivity of odor perception in honeybees (Apis mellifera carnica). Behav Neurosci 115: 632–639.
  13. 13. Laska M, Shepherd GM (2007) Olfactory discrimination ability of CD-1 mice for a large array of enantiomers. Neuroscience 144: 295–301.
  14. 14. Saito H, Chi Q, Zhuang H, Matsunami H, Mainland JD (2009) Odor coding by a mammalian receptor repertoire. Sci Signal 2: ra9.
  15. 15. Benton R, Sachse S, Michnick SW, Vosshall LB (2006) Atypical membrane topology and heteromeric function of Drosophila odorant receptors in vivo. PLoS Biol 4: e20.
  16. 16. Lu T, Qiu YT, Wang G, Kwon JY, Rutzler M, et al. (2007) Odor coding in the maxillary palp of the malaria vector mosquito Anopheles gambiae. Curr Biol 17: 1–12.
  17. 17. Vosshall LB, Wong AM, Axel R (2000) An olfactory sensory map in the fly brain. Cell 102: 147–159.
  18. 18. Neuhaus EM, Gisselmann G, Zhang W, Dooley R, Stortkuhl K, et al. (2005) Odorant receptor heterodimerization in the olfactory system of Drosophila melanogaster. Nat Neurosci 8: 15–17.
  19. 19. Jones WD, Nguyen TA, Kloss B, Lee KJ, Vosshall LB (2005) Functional conservation of an insect odorant receptor gene across 250 million years of evolution. Curr Biol 15: R119–121.
  20. 20. Pitts RJ, Fox AN, Zwiebel LJ (2004) A highly conserved candidate chemoreceptor expressed in both olfactory and gustatory tissues in the malaria vector, Anopheles gambiae. Proc Natl Acad Sci U S A 101: 5058–5063.
  21. 21. Melo AC, Rutzler M, Pitts RJ, Zwiebel LJ (2004) Identification of a chemosensory receptor from the yellow fever mosquito, Aedes aegypti, that is highly conserved and expressed in olfactory and gustatory organs. Chem Senses 29: 403–410.
  22. 22. Xia Y, Zwiebel LJ (2006) Identification and characterization of an odorant receptor from the West Nile Virus mosquito, Culex quinquefasciatus. Insect Biochem Mol Biol 36: 169–176.
  23. 23. Robertson HM, Wanner KW (2006) The chemoreceptor superfamily in the honey bee, Apis mellifera: expansion of the odorant, but not gustatory, receptor family. Genome Res 16: 1395–1403.
  24. 24. Nakagawa T, Sakurai T, Nishioka T, Touhara K (2005) Insect sex-pheromone signals mediated by specific combinations of olfactory receptors. Science 307: 1638–1642.
  25. 25. Krieger J, Grosse-Wilde E, Gohl T, Dewer YM, Raming K, et al. (2004) Genes encoding candidate pheromone receptors in a moth (Heliothis virescens). Proc Natl Acad Sci U S A 101: 11845–11850.
  26. 26. Sato K, Pellegrino M, Nakagawa T, Nakagawa T, Vosshall LB, et al. (2008) Insect olfactory receptors are heteromeric ligand-gated ion channels. Nature 452: 1002–1007.
  27. 27. Wicher D, Schafer R, Bauernfeind R, Stensmyr MC, Heller R, et al. (2008) Drosophila odorant receptors are both ligand-gated and cyclic-nucleotide-activated cation channels. Nature 452: 1007–1011.
  28. 28. Knudsen JT, Tollsten L, Bergstrom G (1993) Floral scents-a checklist of volatile compounds isolated by headspace techniques. Phytochemistry 33: 253–280.
  29. 29. Hall DR, Beevor PS, Cork A, Nesbitt BF, Vale GA (1984) 1-Octen-3-ol, a potent olfactory stimulant and attractant for tsetse isolated from cattle odours. Insect Sci Appl 5: 335–339.
  30. 30. Cork A, Park KC (1996) Identification of electrophysiologically-active compounds for the malaria mosquito, Anopheles gambiae, in human sweat extracts. Med Vet Entomol 10: 269–276.
  31. 31. Pierce AM, Pierce HD Jr, Borden JH, Oehlschlager AC (1989) Production and dynamics of cucujolide pheromones and identification of 1-octen-3-ol as a new aggregation pheromone for Oryzaephilus surinamensis and O. mercator (Coleoptera: Cucujidae). Environ Entomol 18: 747–755.
  32. 32. Kline DL, Allan SA, Bernier UR, Welch CH (2007) Evaluation of the enantiomers of 1-octen-3-ol and 1-octyn-3-ol as attractants for mosquitoes associated with a freshwater swamp in Florida, U.S.A. Med Vet Entomol 21: 323–331.
  33. 33. Syed Z, Leal WS (2007) Maxillary palps are broad spectrum odorant detectors in Culex quinquefasciatus. Chem Senses 32: 727–738.
  34. 34. Blackwell A, Dyer C, Mordue AJ, Wadhams LJ, Mordue W (1996) The role of 1-octen-3-ol as a host-odour attractant for the biting midge, Culicoides impunctatus Goetghebuer, and interactions of 1-octen-3-ol with a volatile pheromone produced by parous female midges. Physiol Entomol 21: 15–19.
  35. 35. Gillies MT (1980) The role of carbon dioxide in host-finding in mosquitoes (Diptera: Culicidae): a review. Bull Entomol Res 70: 525–532.
  36. 36. Grant AJ, Wigton BE, Aghajanian JG, O'Connell RJ (1995) Electrophysiological responses of receptor neurons in mosquito maxillary palp sensilla to carbon dioxide. J Comp Physiol [A] 177: 389–396.
  37. 37. Bohbot J, Pitts RJ, Kwon HW, Rutzler M, Robertson HM, et al. (2007) Molecular characterization of the Aedes aegypti odorant receptor gene family. Insect Mol Biol 16: 525–537.
  38. 38. Hallem E, Fox AN, Zwiebel LJ, Carlson JR (2004) A mosquito odorant receptor tuned to a component of human sweat. Nature 427: 212–213.
  39. 39. Tanaka K, Uda Y, Ono Y, Nakagawa T, Suwa M, et al. (2009) Highly selective tuning of a silkworm olfactory receptor to a key mulberry leaf volatile. Curr Biol 19: 881–890.
  40. 40. Wojtasek H, Hansson BS, Leal WS (1998) Attracted or repelled?–a matter of two neurons, one pheromone binding protein, and a chiral center. Biochem Biophys Res Commun 250: 217–222.
  41. 41. Hill CA, Fox AN, Pitts RJ, Kent LB, Tan PL, et al. (2002) G protein-coupled receptors in Anopheles gambiae. Science 298: 176–178.
  42. 42. Krzywinski J, Wilkerson RC, Besansky NJ (2001) Toward understanding Anophelinae (Diptera, Culicidae) phylogeny: insights from nuclear single-copy genes and the weight of evidence. Syst Biol 50: 540–556.
  43. 43. Wanner KW, Nichols AS, Walden KK, Brockmann A, Luetje CW, et al. (2007) A honey bee odorant receptor for the queen substance 9-oxo-2-decenoic acid. Proc Natl Acad Sci U S A 104: 14383–14388.
  44. 44. Hallem EA, Carlson JR (2006) Coding of odors by a receptor repertoire. Cell 125: 143–160.
  45. 45. Liberles SD, Buck LB (2006) A second class of chemosensory receptors in the olfactory epithelium. Nature 442: 645–650.
  46. 46. Benton R, Vannice KS, Gomez-Diaz C, Vosshall LB (2009) Variant ionotropic glutamate receptors as chemosensory receptors in Drosophila. Cell 136: 149–162.
  47. 47. Turin L (1996) A spectroscopic mechanism for primary olfactory reception. Chem Senses 21: 773–791.
  48. 48. Pophof B (2004) Pheromone-binding proteins contribute to the activation of olfactory receptor neurons in the silkmoths Antheraea polyphemus and Bombyx mori. Chem Senses 29: 117–125.
  49. 49. Grosse-Wilde E, Gohl T, Bouche E, Breer H, Krieger J (2007) Candidate pheromone receptors provide the basis for the response of distinct antennal neurons to pheromonal compounds. Eur J Neurosci 25: 2364–2373.
  50. 50. Laughlin JD, Ha TS, Jones DN, Smith DP (2008) Activation of pheromone-sensitive neurons is mediated by conformational activation of pheromone-binding protein. Cell 133: 1255–1265.
  51. 51. Syed Z, Ishida Y, Kimbrell DA, Leal WS (2006) Pheromone reception in fruit flies expressing a moth's odorant receptor. Proc Natl Acad Sci U S A 103: 16538–16543.
  52. 52. Hallem E, Ho MG, Carlson JR (2004) The molecular basis of odor coding in the Drosophila antenna. Cell 117: 965–979.
  53. 53. Hansen K (1984) Discrimination and production of disparlure enantiomers by the gypsy moth and the nun moth. Physiol Entomol 9: 9–18.
  54. 54. Plettner E, Lazar J, Prestwich EG, Prestwich GD (2000) Discrimination of pheromone enantiomers by two pheromone binding proteins from the gypsy moth Lymantria dispar. Biochemistry 39: 8953–8962.
  55. 55. Gong Y, Pace TC, Castillo C, Bohne C, O'Neill MA, et al. (2009) Ligand-interaction kinetics of the pheromone- binding protein from the gypsy moth, L. dispar: insights into the mechanism of binding and release. Chem Biol 16: 162–172.
  56. 56. Vogt RG, Kohne AC, Dubnau JT, Prestwich GD (1989) Expression of pheromone binding proteins during antennal development in the gypsy moth Lymantria dispar. J Neurosci 9: 3332–3346.
  57. 57. Lartigue A, Gruez A, Spinelli S, Riviere S, Brossut R, et al. (2003) The crystal structure of a cockroach pheromone-binding protein suggests a new ligand binding and release mechanism. J Biol Chem 278: 30213–30218.
  58. 58. Sumikawa K, Houghton M, Emtage JS, Richards BM, Barnard EA (1981) Active multi-subunit ACh receptor assembled by translation of heterologous mRNA in Xenopus oocytes. Nature 292: 862–864.