Synthesis of N-Peptide-6-Amino-d-Luciferin Conjugates with Optimized Fragment Condensation Strategy

Abstract: The synthesis of peptide-luciferin conjugates has a pivotal role in the development of bioluminescent detection systems that are based on the determination of protease enzyme activity. This work describes the optimized synthesis of an N-peptide-6-amino-d-luciferin conjugate (Fmoc-Gly-Pro-6...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Kovács Anita Kármen
Hegyes Péter
Szebeni Gábor
Bogár Krisztián
Puskás László
Tóth Gábor
Dokumentumtípus: Cikk
Megjelent: 2019
Sorozat:INTERNATIONAL JOURNAL OF PEPTIDE RESEARCH AND THERAPEUTICS 25 No. 3
doi:10.1007/s10989-018-9768-8

mtmt:30382079
Online Access:http://publicatio.bibl.u-szeged.hu/16955
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520 3 |a Abstract: The synthesis of peptide-luciferin conjugates has a pivotal role in the development of bioluminescent detection systems that are based on the determination of protease enzyme activity. This work describes the optimized synthesis of an N-peptide-6-amino-d-luciferin conjugate (Fmoc-Gly-Pro-6-amino-d-luciferin) with a simple fragment condensation method in adequate yields. Fmoc-Gly-Pro-6-amino-d-luciferin was produced from a previously synthesized Fmoc-Gly-Pro-OH and also previously synthesized 6-amino-2-cyanobenzothiazole with an optimized method, to which conjugate cysteine was added in an also improved way. The resulting conjugate was successfully used in a bioluminescent system, in vitro, demonstrating the applicability of the method. Graphical Abstract: [Figure not available: see fulltext.]. © 2018, Springer Nature B.V. 
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700 0 1 |a Szebeni Gábor  |e aut 
700 0 1 |a Bogár Krisztián  |e aut 
700 0 1 |a Puskás László  |e aut 
700 0 1 |a Tóth Gábor  |e aut 
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