Ligand-Binding Study of Anopheles gambiae Chemosensory Proteins

被引:51
|
作者
Iovinella, Immacolata [1 ]
Bozza, Francesco [1 ]
Caputo, Beniamino [2 ]
della Torre, Alessandra [2 ]
Pelosi, Paolo [1 ]
机构
[1] Univ Pisa, Dept Agr Food & Environm, I-56124 Pisa, Italy
[2] Univ Roma La Sapienza, Dipartimento Sanita Pubbl & Malattie Infett, I-00185 Rome, Italy
关键词
arthropods; chemical communication; protein expression; sensory appendage protein; tryptophan fluorescence; ODORANT-BINDING; SOLUBLE-PROTEINS; SWISS-MODEL; IMMUNOCYTOCHEMICAL LOCALIZATION; EXPRESSION PATTERN; REGENERATING LEGS; MOLECULAR-CLONING; ANTENNAE; FAMILY; CDNA;
D O I
10.1093/chemse/bjt012
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Chemosensory proteins (CSPs) are a class of small proteins expressed only in arthropods and endowed with heterogeneous functions. Some of them are involved in chemical communications, others in development or other physiological roles. The numbers of CSPs in different species of insects range from 4 in Drosophila to at least 70 in locusts, whereas in other arthropods such as crustaceans and millipedes, only 23 very similar sequences have been reported in each species. We have expressed, in a bacterial system, 5 of the 8 CSPs predicted by the genome of the malaria mosquito Anopheles gambiae, 4 identified at the protein level (SAP1, SAP2, SAP3, and CSP3) and a fifth annotated as part of this work, obtaining the proteins with high yields and in their soluble forms. Purified CSPs have been used to study their ligand-binding properties, both using competitive binding assays and quenching of intrinsic tryptophan fluorescence, in order to get insights into their physiological functions. The agreement between the 2 sets of data supports the assumptions that the ligands, including the fluorescent reporter, bind within the core of the proteins. Their different affinities toward a set of pure chemicals suggest specific roles in chemical communication.
引用
收藏
页码:409 / 419
页数:11
相关论文
共 50 条
  • [1] THERMODYNAMICS OF LIGAND-BINDING TO PROTEINS
    GILL, SJ
    [J]. PURE AND APPLIED CHEMISTRY, 1989, 61 (06) : 1009 - 1020
  • [2] A recipe for ligand-binding proteins
    Giovanna Ghirlanda
    [J]. Nature, 2013, 501 : 177 - 178
  • [3] LIGAND-BINDING TO HEME-PROTEINS - THE EFFECT OF LIGHT ON LIGAND-BINDING IN MYOGLOBIN
    NIENHAUS, GU
    MOURANT, JR
    CHU, K
    FRAUENFELDER, H
    [J]. BIOCHEMISTRY, 1994, 33 (45) : 13413 - 13430
  • [4] Bioinformatics-Based Identification of Chemosensory Proteins in African Malaria Mosquito, Anopheles gambiae
    Zhengxi Li
    Biological Chemistry Division
    [J]. Genomics,Proteomics & Bioinformatics, 2003, (04) : 288 - 298
  • [5] Designing optimal ligand-binding proteins
    Charlotte Harrison
    [J]. Nature Reviews Drug Discovery, 2013, 12 (10) : 742 - 742
  • [6] SIMULATION OF LIGAND-BINDING OF DISSOCIABLE PROTEINS
    BARTHA, F
    BATKE, J
    [J]. ACTA PHYSIOLOGICA ACADEMIAE SCIENTIARUM HUNGARICAE, 1978, 52 (2-3): : 275 - 276
  • [7] DYNAMICS OF LIGAND-BINDING TO HEME PROTEINS
    FRAUENFELDER, H
    [J]. BULLETIN OF THE AMERICAN PHYSICAL SOCIETY, 1975, 20 (03): : 280 - 280
  • [8] Computational design of ligand-binding proteins
    Yang, Wei
    Lai, Luhua
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 2017, 45 : 67 - 73
  • [9] LIGAND-BINDING IN BLUE COPPER PROTEINS
    EHRENSTEIN, D
    ENGELHARD, M
    FILIACI, M
    MCMAHON, B
    NIENHAUS, GU
    SCHARF, B
    [J]. BIOPHYSICAL JOURNAL, 1994, 66 (02) : A273 - A273
  • [10] TUNNELING IN LIGAND-BINDING TO HEME PROTEINS
    ALBERDING, N
    AUSTIN, RH
    BEESON, KW
    CHAN, SS
    EISENSTEIN, L
    FRAUENFELDER, H
    NORDLUND, TM
    [J]. SCIENCE, 1976, 192 (4243) : 1002 - 1004