Literature DB >> 33222203

Disruption of small molecule transporter systems by Transporter-Interfering Chemicals (TICs).

Sascha C T Nicklisch1, Amro Hamdoun2.   

Abstract

Small molecule transporters (SMTs) in the ABC and SLC families are important players in disposition of diverse endo- and xenobiotics. Interactions of environmental chemicals with these transporters were first postulated in the 1990s, and since validated in numerous in vitro and in vivo scenarios. Recent results on the co-crystal structure of ABCB1 with the flame-retardant BDE-100 demonstrate that a diverse range of man-made and natural toxic molecules, hereafter termed transporter-interfering chemicals (TICs), can directly bind to SMTs and interfere with their function. TIC-binding modes mimic those of substrates, inhibitors, modulators, inducers, and possibly stimulants through direct and allosteric mechanisms. Similarly, the effects could directly or indirectly agonize, antagonize or perhaps even prime the SMT system to alter transport function. Importantly, TICs are distinguished from drugs and pharmaceuticals that interact with transporters in that exposure is unintended and inherently variant. Here, we review the molecular mechanisms of environmental chemical interaction with SMTs, the methodological considerations for their evaluation, and the future directions for TIC discovery.
© 2020 Federation of European Biochemical Societies.

Entities:  

Keywords:  ABC transporter; SLC transporter; allosteric; chemosensitization; endogenous substrate competition; environmental; mixtures; signaling interference; small molecule transporter; transporter-interfering chemicals

Mesh:

Substances:

Year:  2020        PMID: 33222203      PMCID: PMC8112642          DOI: 10.1002/1873-3468.14005

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  305 in total

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Journal:  Annu Rev Biophys       Date:  2011       Impact factor: 12.981

4.  Structure of the human multidrug transporter ABCG2.

Authors:  Nicholas M I Taylor; Ioannis Manolaridis; Scott M Jackson; Julia Kowal; Henning Stahlberg; Kaspar P Locher
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5.  Drug-protein hydrogen bonds govern the inhibition of the ATP hydrolysis of the multidrug transporter P-glycoprotein.

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6.  P-glycoprotein is stably inhibited by vanadate-induced trapping of nucleotide at a single catalytic site.

Authors:  I L Urbatsch; B Sankaran; J Weber; A E Senior
Journal:  J Biol Chem       Date:  1995-08-18       Impact factor: 5.157

7.  Pregnane X receptor up-regulation of P-glycoprotein expression and transport function at the blood-brain barrier.

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Review 9.  Hepatobiliary ABC transporters: physiology, regulation and implications for disease.

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1.  Interactions of Environmental Chemicals and Natural Products With ABC and SLC Transporters in the Digestive System of Aquatic Organisms.

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