Insects and other terrestrial arthropods make up over half of all described species on earth. Although the majority of these species have no immediate impact on human life, some are extremely important as disease vectors (i.e. tsetse fly, anopeheline mosquitoes, triatomine bugs, ticks ...), and some have developed into agricultural, forest, and household pests. In addition, spiders and their relatives are of particular pharmacological interest because of their ability to synthesize venoms capable of paralyzing their prey. Chemistry plays a central role in the lives of arthropods.
The aim of this project is to elucidate arthropod chemistry based on critical, biorational considerations, in ways that should lead to the improvement of human health and welfare. In our experimental approach, we plan on developing the use of NMR spectroscopy for the initial study of bioactive samples obtained from arthropod sources. With the ever-increasing sensitivity of NMR spectrometers, and the remarkable power of multidimensional analytical techniques, it is now realistic to carry out useful NMR analyses even on complex mixtures such as those found in spider venoms, or in whole-insect-body extracts. Specifically, our plans include the search for novel neurotoxins in the venoms of spiders and scorpions; the synthesis of newly-discovered venom components for biological screening; the characterization of a predator-produced kairomone which inhibits mosquito oviposition; a search for new anti-insect agents from insect larvae and pupae; elucidation of the structures of new cardiotonic agents from fireflies. Our overall objectives are (1) to discover the chemical basis for important arthropod interactions, (2) to provide the basis for new control techniques applicable to disease vectors, and (3) to find from arthropod sources new biologically active chemotypes which may serve as lead compounds in drug development or vector control.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM053830-33
Application #
7047914
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Program Officer
Schwab, John M
Project Start
1996-08-01
Project End
2008-03-31
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
33
Fiscal Year
2006
Total Cost
$370,289
Indirect Cost
Name
Cornell University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Clark, Valerie C; Harinantenaina, Liva; Zeller, Martin et al. (2012) An endogenous bile acid and dietary sucrose from skin secretions of alkaloid-sequestering poison frogs. J Nat Prod 75:473-8
Caspers, Barbara A; Schroeder, Frank C; Franke, Stephan et al. (2011) Scents of adolescence: the maturation of the olfactory phenotype in a free-ranging mammal. PLoS One 6:e21162
Schroeder, Frank C; Taggi, Andrew E; Gronquist, Matthew et al. (2008) NMR-spectroscopic screening of spider venom reveals sulfated nucleosides as major components for the brown recluse and related species. Proc Natl Acad Sci U S A 105:14283-7
Kim, Jae Hak; Lee, Byong Won; Schroeder, Frank C et al. (2008) Identification of indole glucosinolate breakdown products with antifeedant effects on Myzus persicae (green peach aphid). Plant J 54:1015-26
Bertin, Cecile; Weston, Leslie A; Huang, Tengfang et al. (2007) Grass roots chemistry: meta-tyrosine, an herbicidal nonprotein amino acid. Proc Natl Acad Sci U S A 104:16964-9
Schroeder, Frank C; del Campo, Marta L; Grant, Jacqualine B et al. (2006) Pinoresinol: A lignol of plant origin serving for defense in a caterpillar. Proc Natl Acad Sci U S A 103:15497-501
Gronquist, Matthew; Meinwald, Jerrold; Eisner, Thomas et al. (2005) Exploring uncharted terrain in nature's structure space using capillary NMR spectroscopy: 13 steroids from 50 fireflies. J Am Chem Soc 127:10810-1
Schroeder, Frank C; Weibel, Douglas B; Meinwald, Jerrold (2004) Chiral silylation reagents: determining configuration via NMR-spectroscopic coanalysis. Org Lett 6:3019-22
Attygalle, Athula B; Wu, Xiaogang; Ruzicka, Josef et al. (2004) Defensive chemicals of two species of Trachypachus Motschulski. J Chem Ecol 30:577-88
Teplitski, Max; Eberhard, Anatol; Gronquist, Matthew R et al. (2003) Chemical identification of N-acyl homoserine lactone quorum-sensing signals produced by Sinorhizobium meliloti strains in defined medium. Arch Microbiol 180:494-7

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