VHH Nanobody Versatility against Pentameric Ligand-Gated Ion Channels

被引:0
|
作者
Nemecz, Dorota [1 ]
Nowak, Weronika A. [1 ]
Nemecz, Akos [1 ]
机构
[1] Nicolaus Copernicus Univ Torun, Biochem Dept, Torun, Poland
关键词
GABA(A) RECEPTOR; ANTIBODIES; MECHANISMS; MUTATIONS; DESIGN; GENE;
D O I
10.1021/acs.jmedchem.4c00231
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pentameric ligand-gated ion channels provide rapid chemical-electrical signal transmission between cells in the central and peripheral nervous system. Their dysfunction is associated with many nervous system disorders. They are composed of five identical (homomeric receptors) or homologous (heteromeric receptors) subunits. VHH nanobodies, or single-chain antibodies, are the variable domain, VHH, of antibodies that are composed of the heavy chain only from camelids. Their unique structure results in many specific biochemical and biophysical properties that make them an excellent alternative to conventional antibodies. This Perspective explores the published VHH nanobodies which have been isolated against pentameric ligand-gated ion channel subfamilies. It outlines the genetic and chemical modifications available to alter nanobody function. An assessment of the available functional and structural data indicate that it is feasible to create therapeutic agents and impart, through their modification, a given desired modulatory effect of its target receptor for current stoichiometric-specific VHH nanobodies.
引用
收藏
页码:8502 / 8518
页数:17
相关论文
共 50 条
  • [41] Molecular basis for convergent evolution of glutamate recognition by pentameric ligand-gated ion channels
    Lynagh, Timothy
    Beech, Robin N.
    Lalande, Maryline J.
    Keller, Kevin
    Cromer, Brett A.
    Wolstenholme, Adrian J.
    Laube, Bodo
    SCIENTIFIC REPORTS, 2015, 5
  • [42] Recent Insight into Lipid Binding and Lipid Modulation of Pentameric Ligand-Gated Ion Channels
    Ananchenko, Anna
    Hussein, Toka O. K.
    Mody, Deepansh
    Thompson, Mackenzie J.
    Baenziger, John E.
    BIOMOLECULES, 2022, 12 (06)
  • [43] Phylogenetic conservation of protein-lipid motifs in pentameric ligand-gated ion channels
    Barrantes, Francisco J.
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2015, 1848 (09): : 1796 - 1805
  • [44] ALCOHOL MODULATION VIA ALLOSTERIC TRANSMEMBRANE SITES IN PENTAMERIC LIGAND-GATED ION CHANNELS
    Howard, R. J.
    Heusser, S. A.
    Zhuang, Y.
    Lycksell, M.
    Klement, G.
    Orellana, L.
    Lindahl, E.
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2018, 42 : 60A - 60A
  • [45] Common Anesthetic-binding Site for Inhibition of Pentameric Ligand-gated Ion Channels
    Kinde, Monica N.
    Bu, Weiming
    Chen, Qiang
    Xu, Yan
    Eckenhoff, Roderic G.
    Tang, Pei
    ANESTHESIOLOGY, 2016, 124 (03) : 664 - 673
  • [46] Intramembrane Aromatic Interactions Influence the Lipid Sensitivities of Pentameric Ligand-gated Ion Channels
    Carswell, Casey L.
    Sun, Jiayin
    Baenziger, John E.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290 (04) : 2496 - 2507
  • [47] Investigating allosteric regulation by membrane domains of two pentameric ligand-gated ion channels
    Rogers, Nate
    Varghese, Isabel
    Shaw, Thomas R.
    Stoddard, Andrea K.
    Veatch, Sarah L.
    BIOPHYSICAL JOURNAL, 2023, 122 (03) : 224A - 224A
  • [48] Role of membrane-imbedded residues in the assembly of pentameric ligand-gated ion channels
    Zimmer, E.
    Dopychai, A.
    Schmalzing, G.
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2011, 383 : 61 - 61
  • [49] The dual-gate model for pentameric ligand-gated ion channels activation and desensitization
    Gielen, Marc
    Corringer, Pierre-Jean
    JOURNAL OF PHYSIOLOGY-LONDON, 2018, 596 (10): : 1873 - 1902
  • [50] Role of the Fourth Transmembrane α Helix in the Allosteric Modulation of Pentameric Ligand-Gated Ion Channels
    Carswell, Casey L.
    Henault, Camille M.
    Murlidaran, Sruthi
    Therien, J. P. Daniel
    Juranka, Peter F.
    Surujballi, Julian A.
    Brannigan, Grace
    Baenziger, John E.
    STRUCTURE, 2015, 23 (09) : 1655 - 1664