Rumit Maini

Expansive discovery of chemically diverse structured macrocyclic oligoamides

Accurate de novo design of heterochiral protein–protein interactions

Evolution of Iron(II)‐Finger Peptides by Using a Bipyridyl Amino Acid

The road to fully programmable protein catalysis

Anchor extension: a structure-guided approach to design cyclic peptides targeting enzyme active sites

Expanding and reprogramming the genetic code

Ribosomal synthesis and folding of peptide-helical aromatic foldamer hybrids

Trends in peptide drug discovery

Computational design of a homotrimeric metalloprotein with a trisbipyridyl core

The Current State of Peptide Drug Discovery: Back to the Future?

RNA Display Methods for the Discovery of Bioactive Macrocycles

The RaPID Platform for the Discovery of Pseudo-Natural Macrocyclic Peptides

De Novo Carborane-Containing Macrocyclic Peptides Targeting Human Epidermal Growth Factor Receptor

Semisynthesis of an Active Enzyme by Quantitative Click Ligation

Incorporation of β-amino acids into dihydrofolate reductase by ribosomes having modifications in the peptidyltransferase center

Ribosome-mediated synthesis of natural product-like peptides via cell-free translation

Ribosome-Mediated Incorporation of Dipeptides and Dipeptide Analogues into Proteins in Vitro

Protein Synthesis with Ribosomes Selected for the Incorporation of β-Amino Acids

Ribosomal Formation of Thioamide Bonds in Polypeptide Synthesis