Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/174322
Title: A2A Receptor Homodimer-Disrupting Sequence Efficiently Delivered by a Protease-Resistant, Cyclic CPP Vector
Author: Gallo, Maria
Navarro Brugal, Gemma
Andreu, David
ranco Fernández, Rafael
Keywords: Adenosina
Receptors neurals
Adenosine
Neural receptor
Issue Date: 5-Oct-2019
Publisher: MDPI
Abstract: G-protein-coupled receptors associate into dimers/oligomers whose function is not well understood. One approach to investigate this issue is to challenge oligomerization by peptides replicating transmembrane domains and to study their effect on receptor functionality. The disruptor peptides are typically delivered by means of cell-penetrating vectors such as the human immunodeficiency virus (HIV) transcription trans-activation protein Tat. In this paper we report a cyclic, Tat-like peptide that significantly improves its linear analogue in targeting interreceptor sequences in the transmembrane space. The same cyclic Tat-like vector fused to a transmembrane region not involved in receptor oligomerization was totally ineffective. Besides higher efficacy, the cyclic version has enhanced proteolytic stability, as shown by trypsin digestion experiments. Keywords: GPCR; adenosine receptors; homodimerization; GPCR function; disrupting peptides; trypsin
Note: Reproducció del document publicat a: https://doi.org/10.3390/ijms20194937
It is part of: International Journal of Molecular Sciences, 2019, vol. 20, num. 19
URI: http://hdl.handle.net/2445/174322
Related resource: https://doi.org/10.3390/ijms20194937
ISSN: 1661-6596
Appears in Collections:Articles publicats en revistes (Bioquímica i Fisiologia)
Articles publicats en revistes (Bioquímica i Biomedicina Molecular)

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