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PMID: 1990438 Published · ppublish English Journal Article

Light-directed, spatially addressable parallel chemical synthesis.

Science (New York, N.Y.) ·Vol. 251 ·No. 4995 ·1991-02-15 ·Pages 767-73

Fodor SP, Read JL, Pirrung MC, Stryer L, Lu AT, Solas D

Abstract

Solid-phase chemistry, photolabile protecting groups, and photolithography have been combined to achieve light-directed, spatially addressable parallel chemical synthesis to yield a highly diverse set of chemical products. Binary masking, one of many possible combinatorial synthesis strategies, yields 2n compounds in n chemical steps. An array of 1024 peptides was synthesized in ten steps, and its interaction with a monoclonal antibody was assayed by epifluorescence microscopy. High-density arrays formed by light-directed synthesis are potentially rich sources of chemical diversity for discovering new ligands that bind to biological receptors and for elucidating principles governing molecular interactions. The generality of this approach is illustrated by the light-directed synthesis of a dinucleotide. Spatially directed synthesis of complex compounds could also be used for microfabrication of devices.

MeSH Terms
Amino Acid Sequence Fluorescent Antibody Technique Mathematics Molecular Sequence Data Oligonucleotides/chemical synthesis Oligopeptides/chemical synthesis Photochemistry/methods
Chemicals
Oligonucleotides Oligopeptides
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Fodor S P
Affymax Research Institute, Palo Alto, CA 94304.
Read J L
Pirrung M C
Stryer L
Lu A T
Solas D
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1991-02-15
Pages
767-73
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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