Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractMetabolomic studies of volatiles from tomatoes grown in net-house and open-field conditions    Next AbstractInvestigation of colorimetric biosensor array based on programable surface chemistry of M13 bacteriophage towards artificial nose for volatile organic compound detection: From basic properties of the biosensor to practical application »

Front Endocrinol (Lausanne)


Title:Establishment of Sf9 Transformants Constitutively Expressing PBAN Receptor Variants: Application to Functional Evaluation
Author(s):Lee JM; Hull JJ; Kawai T; Tsuneizumi K; Kurihara M; Tanokura M; Nagata K; Nagasawa H; Matsumoto S;
Address:"Molecular Entomology Laboratory, RIKEN Advanced Science Institute Wako, Japan"
Journal Title:Front Endocrinol (Lausanne)
Year:2012
Volume:20120418
Issue:
Page Number:56 -
DOI: 10.3389/fendo.2012.00056
ISSN/ISBN:1664-2392 (Electronic) 1664-2392 (Linking)
Abstract:"To facilitate further evaluation of pheromone biosynthesis activating neuropeptide receptor (PBANR) functionality and regulation, we generated cultured insect cell lines constitutively expressing green fluorescent protein chimeras of the recently identified Bombyx mori PBANR (BommoPBANR) and Pseudaletia separata PBANR (PsesePBANR) variants. Fluorescent chimeras included the BommoPBANR-A, -B, and -C variants and the PsesePBANR-B and -C variants. Cell lines expressing non-chimeric BommoPBANR-B and -C variants were also generated. Functional evaluation of these transformed cell lines using confocal laser microscopy revealed that a Rhodamine Red-labeled PBAN derivative (RR-C10PBAN(R2K)) specifically co-localized with all of the respective PBANR variants at the plasma membrane. Near complete internalization of the fluorescent RR-C10PBAN(R2K) ligand 30 min after binding was observed in all cell lines except those expressing the BommoPBANR-A variant, in which the ligand/receptor complex remained at the plasma membrane. Fluorescent Ca(2+) imaging further showed that the BommoPBANR-A cell line exhibited drastically different Ca(2+) mobilization kinetics at a number of RR-C10PBAN(R2K) concentrations including 10 muM. These observations demonstrate a clear functional difference between the BommoPBANR-A variant and the BommoPBANR-B and -C variants in terms of receptor regulation and activation of downstream effector molecules. We also found that, contrary to previous reports, ligand-induced internalization of BommoPBANR-B and BommoPBANR-C in cell lines stably expressing these variants occurred in the absence of extracellular Ca(2+)"
Keywords:Gpcr PBAN receptor ligand-induced internalization splice variants stable transformation;
Notes:"PubMed-not-MEDLINELee, Jae Min Hull, J Joe Kawai, Takeshi Tsuneizumi, Kazuhide Kurihara, Masaaki Tanokura, Masaru Nagata, Koji Nagasawa, Hiromichi Matsumoto, Shogo eng Switzerland 2012/06/02 Front Endocrinol (Lausanne). 2012 Apr 18; 3:56. doi: 10.3389/fendo.2012.00056. eCollection 2012"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 27-12-2024