Literature DB >> 33418902

Therapeutic Nanobodies Targeting Cell Plasma Membrane Transport Proteins: A High-Risk/High-Gain Endeavor.

Raf Van Campenhout1, Serge Muyldermans2, Mathieu Vinken1, Nick Devoogdt3, Timo W M De Groof3.   

Abstract

Cell plasma membrane proteins are considered as gatekeepers of the cell and play a major role in regulating various processes. Transport proteins constitute a subclass of cell plasma membrane proteins enabling the exchange of molecules and ions between the extracellular environment and the cytosol. A plethora of human pathologies are associated with the altered expression or dysfunction of cell plasma membrane transport proteins, making them interesting therapeutic drug targets. However, the search for therapeutics is challenging, since many drug candidates targeting cell plasma membrane proteins fail in (pre)clinical testing due to inadequate selectivity, specificity, potency or stability. These latter characteristics are met by nanobodies, which potentially renders them eligible therapeutics targeting cell plasma membrane proteins. Therefore, a therapeutic nanobody-based strategy seems a valid approach to target and modulate the activity of cell plasma membrane transport proteins. This review paper focuses on methodologies to generate cell plasma membrane transport protein-targeting nanobodies, and the advantages and pitfalls while generating these small antibody-derivatives, and discusses several therapeutic nanobodies directed towards transmembrane proteins, including channels and pores, adenosine triphosphate-powered pumps and porters.

Entities:  

Keywords:  cell plasma membrane transport proteins; drug target; nanobodies; therapy

Year:  2021        PMID: 33418902      PMCID: PMC7825061          DOI: 10.3390/biom11010063

Source DB:  PubMed          Journal:  Biomolecules        ISSN: 2218-273X


  128 in total

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Authors:  Gunnar von Heijne
Journal:  Nat Rev Mol Cell Biol       Date:  2006-12       Impact factor: 94.444

Review 2.  Drugability of extracellular targets: discovery of small molecule drugs targeting allosteric, functional, and subunit-selective sites on GPCRs and ion channels.

Authors:  Dimitri E Grigoriadis; Samuel R J Hoare; Sandra M Lechner; Deborah H Slee; John A Williams
Journal:  Neuropsychopharmacology       Date:  2008-09-17       Impact factor: 7.853

3.  Nanobodies that block gating of the P2X7 ion channel ameliorate inflammation.

Authors:  Welbeck Danquah; Catherine Meyer-Schwesinger; Björn Rissiek; Carolina Pinto; Arnau Serracant-Prat; Miriam Amadi; Domenica Iacenda; Jan-Hendrik Knop; Anna Hammel; Philine Bergmann; Nicole Schwarz; Joana Assunção; Wendy Rotthier; Friedrich Haag; Eva Tolosa; Peter Bannas; Eric Boué-Grabot; Tim Magnus; Toon Laeremans; Catelijne Stortelers; Friedrich Koch-Nolte
Journal:  Sci Transl Med       Date:  2016-11-23       Impact factor: 17.956

4.  Camel heavy-chain antibodies: diverse germline V(H)H and specific mechanisms enlarge the antigen-binding repertoire.

Authors:  V K Nguyen; R Hamers; L Wyns; S Muyldermans
Journal:  EMBO J       Date:  2000-03-01       Impact factor: 11.598

Review 5.  Antibodies and venom peptides: new modalities for ion channels.

Authors:  Heike Wulff; Palle Christophersen; Paul Colussi; K George Chandy; Vladimir Yarov-Yarovoy
Journal:  Nat Rev Drug Discov       Date:  2019-05       Impact factor: 84.694

Review 6.  Solute Carrier Transporters as Potential Targets for the Treatment of Metabolic Disease.

Authors:  Tina Schumann; Jörg König; Christine Henke; Diana M Willmes; Stefan R Bornstein; Jens Jordan; Martin F Fromm; Andreas L Birkenfeld
Journal:  Pharmacol Rev       Date:  2020-01       Impact factor: 25.468

7.  Phage display selections for affinity reagents to membrane proteins in nanodiscs.

Authors:  Pawel K Dominik; Anthony A Kossiakoff
Journal:  Methods Enzymol       Date:  2015-03-24       Impact factor: 1.600

8.  NaLi-H1: A universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies.

Authors:  Sandrine Moutel; Nicolas Bery; Virginie Bernard; Laura Keller; Emilie Lemesre; Ario de Marco; Laetitia Ligat; Jean-Christophe Rain; Gilles Favre; Aurélien Olichon; Franck Perez
Journal:  Elife       Date:  2016-07-19       Impact factor: 8.140

9.  Institute collection and analysis of Nanobodies (iCAN): a comprehensive database and analysis platform for nanobodies.

Authors:  Jing Zuo; Jian Li; Rongxin Zhang; Longsheng Xu; Hanhan Chen; Xiaohuan Jia; Zhipeng Su; Linhong Zhao; Xing Huang; Wei Xie
Journal:  BMC Genomics       Date:  2017-10-17       Impact factor: 3.969

Review 10.  Nanobody-Based Delivery Systems for Diagnosis and Targeted Tumor Therapy.

Authors:  Yaozhong Hu; Changxiao Liu; Serge Muyldermans
Journal:  Front Immunol       Date:  2017-11-02       Impact factor: 7.561

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  3 in total

1.  Structural basis of inhibition of a transporter from Staphylococcus aureus, NorC, through a single-domain camelid antibody.

Authors:  Sushant Kumar; Arunabh Athreya; Ashutosh Gulati; Rahul Mony Nair; Ithayaraja Mahendran; Rakesh Ranjan; Aravind Penmatsa
Journal:  Commun Biol       Date:  2021-07-05

Review 2.  Mechanisms Underlying Connexin Hemichannel Activation in Disease.

Authors:  Raf Van Campenhout; Ana Rita Gomes; Timo W M De Groof; Serge Muyldermans; Nick Devoogdt; Mathieu Vinken
Journal:  Int J Mol Sci       Date:  2021-03-28       Impact factor: 6.208

3.  CDR1 Composition Can Affect Nanobody Recombinant Expression Yields.

Authors:  Marco Orlando; Sara Fortuna; Sandra Oloketuyi; Gregor Bajc; Adi Goldenzweig; Ario de Marco
Journal:  Biomolecules       Date:  2021-09-14
  3 in total

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