Molecular-Recognition and Binding Properties of Cyclodextrin-Conjugated Polyrotaxanes

ChemPhysChem ◽  
2006 ◽  
Vol 7 (8) ◽  
pp. 1668-1670 ◽  
Author(s):  
Hak Soo Choi ◽  
Akihiro Takahashi ◽  
Tooru Ooya ◽  
Nobuhiko Yui
Keyword(s):  
Molecular Recognition ◽  
Binding Properties

Molecular recognition between oligopeptides and nucleic acids. DNA sequence specificity and binding properties of an acridine-linked netropsin hybrid ligand

1990 ◽  
Vol 3 (1) ◽  
pp. 26-35 ◽  
Author(s):  
Christian Bailly ◽  
Nicole Helbecque ◽  
Jean-Pierre Hénichart ◽  
Pierre Colson ◽  
Claude Houssier ◽  
...  
Keyword(s):  
Molecular Recognition ◽  
Nucleic Acids ◽  
Dna Sequence ◽  
Sequence Specificity ◽  
Binding Properties ◽  
Dna Sequence Specificity

Molecular Recognition of DNA by Rigid [n]-Polynorbornane-Derived Bifunctional Intercalators:  Synthesis and Evaluation of Their Binding Properties

2007 ◽  
Vol 50 (10) ◽  
pp. 2326-2340 ◽  
Author(s):  
Liisa D. Van Vliet ◽  
Tom Ellis ◽  
Patrick J. Foley ◽  
Ligong Liu ◽  
Frederick M. Pfeffer ◽  
...  
Keyword(s):  
Molecular Recognition ◽  
Binding Properties

scholarly journals Molecular Recognition of Carbohydrates: Evaluation of the Binding Properties of Pyrazole-based receptors and their Comparison with Imidazole- and Indole-based Systems

2012 ◽  
Vol 7 (3) ◽  
pp. 1934578X1200700 ◽  
Author(s):  
Claudia Sonnenberg ◽  
André Hartmann ◽  
Monika Mazik
Keyword(s):  
Molecular Recognition ◽  
Building Blocks ◽  
Binding Studies ◽  
Binding Properties

The aim of the study was to evaluate the potential of pyrazole-based receptors in the complexation of carbohydrates. Representatives of a new series of acyclic pyrazole-based receptors were prepared and their binding properties toward selected mono- and disaccharides evaluated. The results of the binding studies were compared with those obtained for acyclic imidazole- and indole-based receptors. The first binding studies revealed di- vs monosaccharide binding preferences of the new receptors and showed that pyrazole units are useful building blocks for the construction of receptors with interesting binding preferences.

A new family of fluorescent calcium indicators designed to resist leakage or for measuring calcium near membranes

1994 ◽  
Vol 52 ◽  
pp. 168-169
Author(s):  
Martin Poenie ◽  
Akwasi Minta ◽  
Charles Vorndran
Keyword(s):  
Metal Binding ◽  
Acetoxymethyl Ester ◽  
Binding Properties ◽  
Fura 2 ◽  
New Family ◽  
Anion Transporter ◽  
Calcium Indicator ◽  
Calcium Indicators ◽  
High Calcium ◽  
Intracellular Compartmentalization

The use of fura-2 as an intracellular calcium indicator is complicated by problems of rapid dye leakage and intracellular compartmentalization which is due to a probenecid sensitive anion transporter. In addition there is increasing evidence for localized microdomains of high calcium signals which may not be faithfully reported by fura-2.We have developed a new family of fura-2 analogs aimed at addressing some of these problems. These new indicators are based on a modified bapta which can be readily derivatized to produce fura-2 analogs with a variety of new properties. The modifications do not affect the chromophore and have little impact on the spectral and metal binding properties of the indicator. One of these new derivatives known as FPE3 is a zwitterionic analog of fura-2 that can be loaded into cells as an acetoxymethyl ester and whose retention in cells is much improved. The improved retention of FPE3 is important for both cuvettebased measurements of cell suspensions and for calcium imaging.

Fungicidal and binding properties of the natural peptides cecropin B and dermaseptin

1998 ◽  
Vol 36 (5) ◽  
pp. 291-298 ◽  
Author(s):  
DE LUCCA ◽  
BLAND ◽  
JACKS ◽  
GRIMM ◽  
WALSH
Keyword(s):  
Binding Properties ◽  
Cecropin B ◽  
Natural Peptides
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