Published June 2016
| Version v1
Journal article
Rational design of improved dienophiles for in vivo tetrazine-trans-cyclooctene ligation
- 1. Interdisciplinary Center for Scientific Computing, Im Neuenheimer Feld 205, 69120 Heidelberg (Germany)
- 2. Organisch-Chemisches Institut, Im Neuenheimer Feld 270, 69120 Heidelberg (Germany)
Description
The inverse electron-demand Diels–Alder reaction of trans-cyclooctene and sym-tetrazine is a bioorthogonal reaction which has found widespread applications during the last decade, e.g. for fluorescent labeling of living cells. However, the use of this reaction is still limited due to the rapid isomerization of trans-cyclooctene to its unreactive cis-conformer. Using computational methods, we have derived two optimized derivatives of trans-cyclooctene, which pave the road to more efficient in vivo labeling of arbitrary proteins.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.cplett.2016.04.044Additional details
Identifiers
- DOI
- 10.1016/j.cplett.2016.04.044;
- PII
- S0009261416302305;
Publishing Information
- Journal Title
- Chemical Physics Letters
- Journal Volume
- 654
- Journal Page Range
- p. 6-8
- ISSN
- 0009-2614
- CODEN
- CHPLBC
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 51123265
- Subject category
- S60: APPLIED LIFE SCIENCES; S74: ATOMIC AND MOLECULAR PHYSICS;
- Descriptors DEI
- DEMAND; DESIGN; FLUORESCENCE; IN VIVO; ISOMERIZATION; LABELLING; ROADS
- Descriptors DEC
- CHEMICAL REACTIONS; EMISSION; LUMINESCENCE; PHOTON EMISSION
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier B.V. All rights reserved.