Benjamin Lerner
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Benjamin Lerner has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Arpita Paikar
Department of Molecular Chemistry and Materials Science Weizmann Institute of Science Rehovot 7610001 Israel
2 shared publications - Guy Shmul
Department of Chemical Research Support Weizmann Institute of Science Rehovot 7610001 Israel
2 shared publications - Sergey N. Semenov
Department of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot, Israel
2 shared publications - Xiaoming Miao
Department of Molecular Chemistry and Materials Science Weizmann Institute of Science Rehovot 7610001 Israel
2 shared publications - Yael Diskin-Posner
Weizmann Institute of Science
2 shared publications
Latest Publications
- 18 June 2021
- Published by Wiley in Angewandte Chemie
- Vol. 133 (37) , 20529-20538
Kinetic Selection in the Out‐of‐Equilibrium Autocatalytic Reaction Networks that Produce Macrocyclic Peptides
Autocatalytic reaction networks are instrumental for validating scenarios for the emergence of life on Earth and for synthesizing life de novo. Here, we demonstrate that dimeric thioesters of tripeptides with the general structure (Cys‐Xxx‐Gly‐SEt)2 form strongly interconnected autocatalytic reaction networks that predominantly generate macrocyclic peptides up to 69 amino acids long. Some macrocycles of 6–12 amino acids were isolated from the product pool and were characterized by NMR spectroscopy and single‐crystal X‐ray analysis. We studied the autocatalytic formation of macrocycles in a flow reactor in the presence of acrylamide, whose conjugate addition to thiols served as a model “removal” reaction. These results indicate that even not template‐assisted autocatalytic production combined with competing removal of molecular species in an open compartment could be a feasible route for selecting functional molecules during the pre‐Darwinian stages of molecular evolution.
- 18 June 2021
- Published by Wiley in Angewandte Chemie
- Vol. 133 (37) , 20529-20538
Kinetic Selection in the Out‐of‐Equilibrium Autocatalytic Reaction Networks that Produce Macrocyclic Peptides
Autocatalytic reaction networks are instrumental for validating scenarios for the emergence of life on Earth and for synthesizing life de novo. Here, we demonstrate that dimeric thioesters of tripeptides with the general structure (Cys‐Xxx‐Gly‐SEt)2 form strongly interconnected autocatalytic reaction networks that predominantly generate macrocyclic peptides up to 69 amino acids long. Some macrocycles of 6–12 amino acids were isolated from the product pool and were characterized by NMR spectroscopy and single‐crystal X‐ray analysis. We studied the autocatalytic formation of macrocycles in a flow reactor in the presence of acrylamide, whose conjugate addition to thiols served as a model “removal” reaction. These results indicate that even not template‐assisted autocatalytic production combined with competing removal of molecular species in an open compartment could be a feasible route for selecting functional molecules during the pre‐Darwinian stages of molecular evolution.
- 18 June 2021
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 60 (37) , 20366-20375
Kinetic Selection in the Out‐of‐Equilibrium Autocatalytic Reaction Networks that Produce Macrocyclic Peptides
Autocatalytic reaction networks are instrumental for validating scenarios for the emergence of life on Earth and for synthesizing life de novo. Here, we demonstrate that dimeric thioesters of tripeptides with the general structure (Cys‐Xxx‐Gly‐SEt)2 form strongly interconnected autocatalytic reaction networks that predominantly generate macrocyclic peptides up to 69 amino acids long. Some macrocycles of 6–12 amino acids were isolated from the product pool and were characterized by NMR spectroscopy and single‐crystal X‐ray analysis. We studied the autocatalytic formation of macrocycles in a flow reactor in the presence of acrylamide, whose conjugate addition to thiols served as a model “removal” reaction. These results indicate that even not template‐assisted autocatalytic production combined with competing removal of molecular species in an open compartment could be a feasible route for selecting functional molecules during the pre‐Darwinian stages of molecular evolution.
- 18 June 2021
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 60 (37) , 20366-20375
Kinetic Selection in the Out‐of‐Equilibrium Autocatalytic Reaction Networks that Produce Macrocyclic Peptides
Autocatalytic reaction networks are instrumental for validating scenarios for the emergence of life on Earth and for synthesizing life de novo. Here, we demonstrate that dimeric thioesters of tripeptides with the general structure (Cys‐Xxx‐Gly‐SEt)2 form strongly interconnected autocatalytic reaction networks that predominantly generate macrocyclic peptides up to 69 amino acids long. Some macrocycles of 6–12 amino acids were isolated from the product pool and were characterized by NMR spectroscopy and single‐crystal X‐ray analysis. We studied the autocatalytic formation of macrocycles in a flow reactor in the presence of acrylamide, whose conjugate addition to thiols served as a model “removal” reaction. These results indicate that even not template‐assisted autocatalytic production combined with competing removal of molecular species in an open compartment could be a feasible route for selecting functional molecules during the pre‐Darwinian stages of molecular evolution.