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A Combined NMR and Computational Approach to Determine the RGDechi‐hCit‐α v β 3 Integrin Recognition Mode in Isolated Cell Membranes
Author(s) -
Farina Biancamaria,
de Paola Ivan,
Russo Luigi,
Capasso Domenica,
Liguoro Annamaria,
Gatto Annarita Del,
Saviano Michele,
Pedone Paolo V.,
Di Gaetano Sonia,
Malgieri Gaetano,
Zaccaro Laura,
Fattorusso Roberto
Publication year - 2016
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201503126
Subject(s) - integrin , internalization , microbiology and biotechnology , biology , peptide , membrane , computational biology , cell , chemistry , biochemistry
The critical role of integrins in tumor progression and metastasis has stimulated intense efforts to identify pharmacological agents that can modulate integrin function. In recent years, α v β 3 and α v β 5 integrin antagonists were demonstrated to be effective in blocking tumor progression. RGDechi‐hCit, a chimeric peptide containing a cyclic RGD motif linked to an echistatin C‐terminal fragment, is able to recognize selectively α v β 3 integrin both in vitro and in vivo. High‐resolution molecular details of the selective α v β 3 recognition of the peptide are certainly required, nonetheless RGDechi‐hCit internalization limited the use of classical in cell NMR experiments. To overcome such limitations, we used WM266 isolated cellular membranes to accomplish a detailed NMR interaction study that, combined with a computational analysis, provides significant structural insights into α v β 3 molecular recognition by RGDechi‐hCit. Remarkably, on the basis of the identified molecular determinants, we design a RGDechi‐hCit mutant that is selective for α v β 5 integrin.