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.2016.04.044

Additional 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.