reusable liposome array and its application to assay of growth-hormone-related peptides

We describe a reusable liposome array based on the formation of cleavable disulfide cross-links between liposomes and the surface of a glass slip. The N-succinimidyl 3-(2-pyridyldithio)-propionate (SPDP)-modified liposomes encapsulating a pH-sensitive fluorescence dye were immobilized on a 3-mercapt...

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Veröffentlicht in:Analytical and bioanalytical chemistry 2010-06, Vol.397 (3), p.1377-1381
Hauptverfasser: Shoji, Atsushi, Sugimoto, Erika, Orita, Sayaka, Nozawa, Keiichiro, Yanagida, Akio, Shibusawa, Yoichi, Sugawara, Masao
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container_end_page 1381
container_issue 3
container_start_page 1377
container_title Analytical and bioanalytical chemistry
container_volume 397
creator Shoji, Atsushi
Sugimoto, Erika
Orita, Sayaka
Nozawa, Keiichiro
Yanagida, Akio
Shibusawa, Yoichi
Sugawara, Masao
description We describe a reusable liposome array based on the formation of cleavable disulfide cross-links between liposomes and the surface of a glass slip. The N-succinimidyl 3-(2-pyridyldithio)-propionate (SPDP)-modified liposomes encapsulating a pH-sensitive fluorescence dye were immobilized on a 3-mercaptopropyltrimethoxysilane (MTS)-modified glass slip through the formation of disulfide bonds. The regeneration of a used slip was performed by the lysis of immobilized liposomes with Triton X-100 and the cleavage of disulfide bonds by reduction with TCEP, followed by immobilization of SPDP-modified liposomes. The regeneration steps did not affect the fluorescence intensity of re-immobilized liposomes. The liposome array was applied to simultaneous quantification of growth hormone related peptides, i.e., GHRF and somatostatin, in a mixture. After optimizing the assay condition, the method allowed quantification of GHRF and somatostatin in concentration ranges from 0.5 × 10⁻⁹ to 0.5 × 10⁻⁷ g/mL with detection limits of 2 × 10⁻¹⁰ and 3 × 10⁻¹⁰ g/mL, respectively.
doi_str_mv 10.1007/s00216-010-3615-x
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After optimizing the assay condition, the method allowed quantification of GHRF and somatostatin in concentration ranges from 0.5 × 10⁻⁹ to 0.5 × 10⁻⁷ g/mL with detection limits of 2 × 10⁻¹⁰ and 3 × 10⁻¹⁰ g/mL, respectively.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><pmid>20306177</pmid><doi>10.1007/s00216-010-3615-x</doi><tpages>5</tpages></addata></record>
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source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Analysis
Analytical Chemistry
Arrays
Assaying
Avidin - chemistry
Biochemistry
Biosensing Techniques - methods
Characterization and Evaluation of Materials
Chemical properties
Chemistry
Chemistry and Materials Science
Cross-Linking Reagents - chemistry
Crosslinking
Disulfides - chemistry
Exact sciences and technology
Fluorescence
Fluorimetry
Food Science
Glass - chemistry
Gramicidin - chemistry
Gramicidin channel
Gramicidins
Growth
Growth Hormone - analysis
Growth hormone releasing factor (GHRF)
Growth Hormone-Releasing Hormone - analysis
Hydrogen-ion concentration
Immunoassay
Immunoassay - methods
Laboratory Medicine
Limit of Detection
Liposome array
Liposomes
Liposomes - chemistry
Materials
Mathematical analysis
Methods
Monitoring/Environmental Analysis
Peptides
Physiological aspects
Production processes
Properties
Proteins
Reusable
Sensitivity and Specificity
Somatostatin
Somatostatin - analysis
Somatotropin
Somatotropin releasing hormone
Spectrometric and optical methods
Surface active agents
Technical Note
title reusable liposome array and its application to assay of growth-hormone-related peptides
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