The highly sequence-selective molecular recognition of proteins and peptides in Nature inspires and informs the development of synthetic receptors to mimic, measure, and modulate these processes. This chapter focuses on the cucurbit[n]urils, which have been particularly powerful in this regard. We describe the discovery and elaboration of the sequence-selective recognition of peptides by cucurbit[n]urils. In addition, we overview the development of this supramolecular chemistry into myriad applications and the extension to protein recognition. Finally, we compare the binding properties of synthetic receptors with those of natural N-recognins, proteases, and other sequence-selective protein receptors. The strong correlation between natural a...
This paper describes the molecular recognition of the tripeptide Tyr-Leu-Ala by the synthetic recept...
Cucurbit[7]uril forms very strong complex with zwitterionic dipeptide Phe-Gly with affinity exceedin...
The creation of synthetic molecules having selective peptide-binding properties seen in biological s...
At the forefront of the endeavor to understand and manipulate living systems is the design and study...
Sequence-selective recognition is an important goal for synthetic receptors binding to proteins with...
Chemists have long attempted to prepare synthetic receptors (SRs) that can bind natural targets with...
This Article describes the molecular recognition of peptides containing an N-terminal methionine (Me...
In this chapter, an overview is provided of the different concepts of cucurbiturils directly interac...
This paper describes the molecular recognition of phenylalanine derivatives and their peptides by th...
This paper describes the molecular recognition of amino acids by cucurbit[8]uril (Q8) and by the 1:1...
This Article describes the molecular recognition of peptides containing an N-terminal methionine (Me...
Cucurbit[n]urils (CB[n]s) provide a class of macrocycles that are able to form stable host–guest com...
Biochemical studies have revealed the propensity of aromatic amino acid residues to mediate importan...
This paper describes the molecular recognition of the tripeptide Tyr-Leu-Ala by the synthetic recept...
Cucurbit[7]uril forms very strong complex with zwitterionic dipeptide Phe-Gly with affinity exceedin...
The creation of synthetic molecules having selective peptide-binding properties seen in biological s...
At the forefront of the endeavor to understand and manipulate living systems is the design and study...
Sequence-selective recognition is an important goal for synthetic receptors binding to proteins with...
Chemists have long attempted to prepare synthetic receptors (SRs) that can bind natural targets with...
This Article describes the molecular recognition of peptides containing an N-terminal methionine (Me...
In this chapter, an overview is provided of the different concepts of cucurbiturils directly interac...
This paper describes the molecular recognition of phenylalanine derivatives and their peptides by th...
This paper describes the molecular recognition of amino acids by cucurbit[8]uril (Q8) and by the 1:1...
This Article describes the molecular recognition of peptides containing an N-terminal methionine (Me...
Cucurbit[n]urils (CB[n]s) provide a class of macrocycles that are able to form stable host–guest com...
Biochemical studies have revealed the propensity of aromatic amino acid residues to mediate importan...
This paper describes the molecular recognition of the tripeptide Tyr-Leu-Ala by the synthetic recept...
Cucurbit[7]uril forms very strong complex with zwitterionic dipeptide Phe-Gly with affinity exceedin...
The creation of synthetic molecules having selective peptide-binding properties seen in biological s...