Versatile synthesis of fluorescent, cross-linked peptides as biological probes with the advantage of high helix content

Kazuhisa Fujimoto; Masaoki Kajino; Masahiko Inouye

doi:10.1007/s11164-012-0651-5

Versatile synthesis of fluorescent, cross-linked peptides as biological probes with the advantage of high helix content

Kazuhisa Fujimoto^*, Masaoki Kajino, Masahiko Inouye

^*Corresponding author for this work

Member of the Board

Research output: Contribution to journal › Article › peer-review

4 Scopus citations

Abstract

A variety of fluorophores were introduced at the N-termini of short peptides for use as biological-probes. The fluorescent peptides were cross-linked with a diacetylenic cross-linking agent between the amino acid side chains of ornithine (Orn) residues to produce peptides with high helix content.

Original language	English
Pages (from-to)	311-319
Number of pages	9
Journal	Research on Chemical Intermediates
Volume	39
Issue number	1
DOIs	https://doi.org/10.1007/s11164-012-0651-5
State	Published - 2013/01

Keywords

Biological probe
Fluorescence labeling
Fluorophore
Short helical peptide

ASJC Scopus subject areas

General Chemistry

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10.1007/s11164-012-0651-5

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title = "Versatile synthesis of fluorescent, cross-linked peptides as biological probes with the advantage of high helix content",

abstract = "A variety of fluorophores were introduced at the N-termini of short peptides for use as biological-probes. The fluorescent peptides were cross-linked with a diacetylenic cross-linking agent between the amino acid side chains of ornithine (Orn) residues to produce peptides with high helix content.",

keywords = "Biological probe, Fluorescence labeling, Fluorophore, Short helical peptide",

author = "Kazuhisa Fujimoto and Masaoki Kajino and Masahiko Inouye",

note = "Funding Information: Acknowledgments This work was partially supported by Grants-in-Aid for Scientific Research (B) (22350072) and for Young Scientists (B) (23750184) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan.",

year = "2013",

month = jan,

doi = "10.1007/s11164-012-0651-5",

language = "英語",

volume = "39",

pages = "311--319",

journal = "Research on Chemical Intermediates",

issn = "0922-6168",

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T1 - Versatile synthesis of fluorescent, cross-linked peptides as biological probes with the advantage of high helix content

AU - Fujimoto, Kazuhisa

AU - Kajino, Masaoki

AU - Inouye, Masahiko

N1 - Funding Information: Acknowledgments This work was partially supported by Grants-in-Aid for Scientific Research (B) (22350072) and for Young Scientists (B) (23750184) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan.

PY - 2013/1

Y1 - 2013/1

N2 - A variety of fluorophores were introduced at the N-termini of short peptides for use as biological-probes. The fluorescent peptides were cross-linked with a diacetylenic cross-linking agent between the amino acid side chains of ornithine (Orn) residues to produce peptides with high helix content.

AB - A variety of fluorophores were introduced at the N-termini of short peptides for use as biological-probes. The fluorescent peptides were cross-linked with a diacetylenic cross-linking agent between the amino acid side chains of ornithine (Orn) residues to produce peptides with high helix content.

KW - Biological probe

KW - Fluorescence labeling

KW - Fluorophore

KW - Short helical peptide

UR - http://www.scopus.com/inward/record.url?scp=84871731086&partnerID=8YFLogxK

U2 - 10.1007/s11164-012-0651-5

DO - 10.1007/s11164-012-0651-5

M3 - 学術論文

AN - SCOPUS:84871731086

SN - 0922-6168

VL - 39

SP - 311

EP - 319

JO - Research on Chemical Intermediates

JF - Research on Chemical Intermediates

IS - 1

ER -

Versatile synthesis of fluorescent, cross-linked peptides as biological probes with the advantage of high helix content

Abstract

Keywords

ASJC Scopus subject areas

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