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PMID: 15858647 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Arginine magic with new counterions up the sleeve.

Organic & biomolecular chemistry ·Vol. 3 ·No. 9 ·2005-05-07 ·Pages 1659-69

Nishihara M, Perret F, Takeuchi T, Futaki S, Lazar AN, Coleman AW, Sakai N, Matile S

Abstract

The elusive questions how arginine-rich sequences allow peptides and proteins to penetrate cells or to form voltage-gated ion channels are controversial topics of current scientific concern. The possible contributions of exchangeable counterions to these puzzling processes remain underexplored. The objective of this report is to clarify scope and limitations of certain counteranions to modulate cellular uptake and anion carrier activity of oligo/polyarginines. The key finding is that the efficiency of counteranion activators depends significantly on many parameters such as activator-membrane and activator-carrier interactions. This finding is important because it suggests that counteranions can be used to modulate not only efficiency but also selectivity. Specifically, activator efficiencies are found to increase with increasing aromatic surface of the activator, decreasing size of the transported anion, increasing carrier concentration as well as increasing membrane fluidity. Efficiency sequences depend on membrane composition with coronene > pyrene >>fullerene > calix[4]arene carboxylates in fluid and crystalline DPPC contrasting to fullerene > calix[4]arene approximately coronene > pyrene carboxylates in EYPC with or without cholesterol or ergosterol. In HeLa cells, the efficiency of planar activators (pyrene) exceeds that of spherical activators (fullerenes, calixarenes). Polyarginine complexes with pyrene and coronene activators exhibit exceptional excimer emission. Decreasing excimer emission with increasing ionic strength reveals dominant hydrophobic interactions with the most efficient carboxylate activators. Dominance of ion pairing with the inefficient high-affinity sulfate activators is corroborated by the reversed dependence on ionic strength. These findings on activator-carrier and activator-membrane interactions are discussed as supportive of arene-templated guanidinium-carboxylate pairing and interface-directed translocation as possible origins of the superb performance of higher arene carboxylates as activators.

MeSH Terms
Arginine/chemistry Phospholipids/chemistry
Chemicals
Phospholipids Arginine
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Nishihara Masamichi
Department of Organic Chemistry, University of Geneva, Geneva, Switzerland.
Perret Florent
Takeuchi Toshihide
Futaki Shiroh
Lazar Adina N
Coleman Anthony W
Sakai Naomi
Matile Stefan
Article Info
Journal
Organic & biomolecular chemistry
Abbr.
Org Biomol Chem
ISSN
1477-0520
Published
2005-05-07
Epub
2005-00-07
Pages
1659-69
Language
English
Region
England
NLM ID
101154995
Subset
IM
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