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research article

Solid-phase peptide synthesis in 384-well plates

Schuttel, Mischa
•
Will, Edward  
•
Sangouard, Gontran  
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January 14, 2024
Journal Of Peptide Science

Newer solid-phase peptide synthesis and release strategies enable the production of short peptides with high purity, allowing direct screening for desired bioactivity without prior chromatographic purification. However, the maximum number of peptides that can currently be synthesized per microplate reactor is 96, allowing the parallel synthesis of 384 peptides in modern devices that have space for 4 microplate reactors. To synthesize larger numbers of peptides, we modified a commercially available peptide synthesizer to enable the production of peptides in 384-well plates, which allows the synthesis of 1,536 peptides in one run (4 x 384 peptides). We report new hardware components and customized software that allowed for the synthesis of 1,536 short peptides in good quantity (average > 0.5 mu mol), at high concentration (average > 10 mM), and decent purity without purification (average > 80%). The high-throughput peptide synthesis, which we developed with peptide drug development in mind, may be widely used for peptide library synthesis and screening, antibody epitope scanning, epitope mimetic development, or protease/kinase substrate screening.

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Type
research article
DOI
10.1002/psc.3555
Web of Science ID

WOS:001143070300001

Author(s)
Schuttel, Mischa
Will, Edward  
Sangouard, Gontran  
Zarda, Anne Sofie Luise  
Habeshian, Sevan  
Nielsen, Alexander Lund  
Heinis, Christian  
Date Issued

2024-01-14

Published in
Journal Of Peptide Science
Subjects

Life Sciences & Biomedicine

•

Physical Sciences

•

384-Well Plate

•

Combinatorial Chemistry

•

Peptide Library

•

Peptide Synthesis

•

Spps

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LPPT  
FunderGrant Number

Swiss National Science Foundation

European Research Council (ERC)

192368

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Available on Infoscience
February 21, 2024
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/205068
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