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« Previous Abstract"Behavioural, physiological and molecular changes in alloparental caregivers may be responsible for selection response for female reproductive investment in honey bees"    Next AbstractDifferences in ASP1 expression and binding dynamics to queen mandibular pheromone HOB between Apis mellifera and Apis cerana workers reveal olfactory adaptation to colony organization »

Int J Biol Macromol


Title:Mechanistic insight into binding interaction between chemosensory protein 4 and volatile larval pheromones in honeybees (Apis mellifera)
Author(s):Wu F; Feng Y; Han B; Hu H; Feng M; Meng L; Ma C; Yu L; Li J;
Address:"Institute of Apicultural Research/Key Laboratory of Pollinating Insect Biology, Ministry of Agriculture, Chinese Academy of Agricultural Science, Beijing 100081, PR China. State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, PR China. Anhui Agricultural University, Anhui 230036, PR China. Electronic address: yulinsheng@ahau.edu.cn. Institute of Apicultural Research/Key Laboratory of Pollinating Insect Biology, Ministry of Agriculture, Chinese Academy of Agricultural Science, Beijing 100081, PR China. Electronic address: apislijk@126.com"
Journal Title:Int J Biol Macromol
Year:2019
Volume:20190906
Issue:
Page Number:553 - 563
DOI: 10.1016/j.ijbiomac.2019.09.041
ISSN/ISBN:1879-0003 (Electronic) 0141-8130 (Linking)
Abstract:"Honeybees communicate with members of their intra-species via pheromones. The volatile pheromones, beta-ocimene and allo-ocimene, are the primary signals of larvae to beg for the care from the nurses. Of the odorant binding proteins (OBPs)/chemosensory proteins (CSPs), CSP4 has the best affinity with beta-ocimene and allo-ocimene. To reveal the binding mechanism of CPS4 with them, fluorescent quenching, UV absorption spectra, circular dichroism (CD) spectra, isothermal titration calorimetry (ITC), molecular docking, molecular dynamic (MD) simulation, and site-directed mutagenesis were applied. The quenching constant Ksv decreased with temperature increase, and the interaction distance was 2.73?ª+nm and 2.43?ª+nm (<10?ª+nm), indicating that beta-ocimene and allo-ocimene could form stable complexes with CSP4. The observed big up tri, openH?ª+?ª+0 of thermodynamics suggest the main driving forces are electrostatic or hydrophobic force. All above thermodynamics findings are in line with the results of ITC experiments. Furthermore, molecular docking, MD simulation and site-directed mutagenesis indicate the binding cavities are located at cavity 1 in C-terminal of CSP4, where Tyr98 and Asp67 are vital amino acids in maintaining the stable form of protein and larval pheromones, and electrostatic energies are the main driving forces. Our findings gain novel insight into the binding mechanism of chemosensory protein with volatile larval pheromones and are important for understanding olfactory interaction of honeybees"
Keywords:Animals Bees/*chemistry/metabolism Insect Proteins/*chemistry/metabolism Larva/chemistry/metabolism *Molecular Docking Simulation Pheromones/*chemistry/metabolism Chemosensory proteins Fluorescence spectroscopy Molecular docking Quenching mechanism Site-d;
Notes:"MedlineWu, Fan Feng, Yilu Han, Bin Hu, Han Feng, Mao Meng, Lifeng Ma, Chuan Yu, Linsheng Li, Jianke eng Netherlands 2019/09/10 Int J Biol Macromol. 2019 Dec 1; 141:553-563. doi: 10.1016/j.ijbiomac.2019.09.041. Epub 2019 Sep 6"

 
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Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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