Lyophilization and enhanced stability of fluorescent protein nanoparticles

Kyung Rim Kim, Keum Young Ahn, Jin Seung Park, Kyung Eun Lee, Hyesung Jeon, Jeewon Lee

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Protein nanoparticles (PNPs) that are nanostructured biomaterials with intrinsic biological function have been widely employed as three-dimensional nanobiomaterials for sensitive bioassays, MRI contrast, semiconductor devices, template for hybrid materials, etc., and stable and long-term maintenance of PNPs seems to be of crucial importance. We evaluated the stability of PNPs and the efficacy of lyophilization for the long-term stability of PNPs, especially using green fluorescent protein nanoparticles (gFPNPs) as a model PNP. Fluorescence intensities and TEM images of gFPNPs were analyzed to monitor their functional and structural stabilities. Unlike the green fluorescent protein monomers (eGFP) that were gradually inactivated in aqueous solution, gFPNP in the same aqueous solution retained the initial fluorescence activity and spherical nanoparticle structure even for 2. weeks at 4. °C. To ensure stable and long-term maintenance of gFPNPs, gFPNPs in aqueous solution were converted to the dried solid forms through lyophilization. It is notable that fluorescence activity and nanoparticle structure of gFPNPs that were lyophilized with both Tween 80 and sucrose were very stably maintained even for 10. weeks at various storage temperatures (-20. °C, 4. °C, 25. °C, and 37. °C). During the period of 10. weeks, the fluorescence of gFPNP was always more than 80% level of initial fluorescence at a wide range of temperature. Although this stability study was focused on gFPNPs, the developed optimal lyophilization conditions for gFPNPs can be applied in general to stable and long-term maintenance of many other PNP-derived biomaterials.

Original languageEnglish
Pages (from-to)225-229
Number of pages5
JournalBiochemical and Biophysical Research Communications
Volume408
Issue number2
DOIs
Publication statusPublished - 2011 May 6

Fingerprint

Freeze Drying
Protein Stability
Nanoparticles
Green Fluorescent Proteins
Proteins
Fluorescence
Biocompatible Materials
Semiconductors
Temperature
Polysorbates
Bioassay
Hybrid materials
Semiconductor devices

Keywords

  • Fluorescent protein nanoparticles
  • Lyophilization
  • Protein nanoparticle structure
  • Stability

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Cell Biology
  • Molecular Biology

Cite this

Lyophilization and enhanced stability of fluorescent protein nanoparticles. / Kim, Kyung Rim; Ahn, Keum Young; Park, Jin Seung; Lee, Kyung Eun; Jeon, Hyesung; Lee, Jeewon.

In: Biochemical and Biophysical Research Communications, Vol. 408, No. 2, 06.05.2011, p. 225-229.

Research output: Contribution to journalArticle

Kim, Kyung Rim ; Ahn, Keum Young ; Park, Jin Seung ; Lee, Kyung Eun ; Jeon, Hyesung ; Lee, Jeewon. / Lyophilization and enhanced stability of fluorescent protein nanoparticles. In: Biochemical and Biophysical Research Communications. 2011 ; Vol. 408, No. 2. pp. 225-229.
@article{b19c9fd05e994887b2a60b6502b69649,
title = "Lyophilization and enhanced stability of fluorescent protein nanoparticles",
abstract = "Protein nanoparticles (PNPs) that are nanostructured biomaterials with intrinsic biological function have been widely employed as three-dimensional nanobiomaterials for sensitive bioassays, MRI contrast, semiconductor devices, template for hybrid materials, etc., and stable and long-term maintenance of PNPs seems to be of crucial importance. We evaluated the stability of PNPs and the efficacy of lyophilization for the long-term stability of PNPs, especially using green fluorescent protein nanoparticles (gFPNPs) as a model PNP. Fluorescence intensities and TEM images of gFPNPs were analyzed to monitor their functional and structural stabilities. Unlike the green fluorescent protein monomers (eGFP) that were gradually inactivated in aqueous solution, gFPNP in the same aqueous solution retained the initial fluorescence activity and spherical nanoparticle structure even for 2. weeks at 4. °C. To ensure stable and long-term maintenance of gFPNPs, gFPNPs in aqueous solution were converted to the dried solid forms through lyophilization. It is notable that fluorescence activity and nanoparticle structure of gFPNPs that were lyophilized with both Tween 80 and sucrose were very stably maintained even for 10. weeks at various storage temperatures (-20. °C, 4. °C, 25. °C, and 37. °C). During the period of 10. weeks, the fluorescence of gFPNP was always more than 80{\%} level of initial fluorescence at a wide range of temperature. Although this stability study was focused on gFPNPs, the developed optimal lyophilization conditions for gFPNPs can be applied in general to stable and long-term maintenance of many other PNP-derived biomaterials.",
keywords = "Fluorescent protein nanoparticles, Lyophilization, Protein nanoparticle structure, Stability",
author = "Kim, {Kyung Rim} and Ahn, {Keum Young} and Park, {Jin Seung} and Lee, {Kyung Eun} and Hyesung Jeon and Jeewon Lee",
year = "2011",
month = "5",
day = "6",
doi = "10.1016/j.bbrc.2011.03.123",
language = "English",
volume = "408",
pages = "225--229",
journal = "The BMJ",
issn = "0730-6512",
publisher = "Kluwer Academic Publishers",
number = "2",

}

TY - JOUR

T1 - Lyophilization and enhanced stability of fluorescent protein nanoparticles

AU - Kim, Kyung Rim

AU - Ahn, Keum Young

AU - Park, Jin Seung

AU - Lee, Kyung Eun

AU - Jeon, Hyesung

AU - Lee, Jeewon

PY - 2011/5/6

Y1 - 2011/5/6

N2 - Protein nanoparticles (PNPs) that are nanostructured biomaterials with intrinsic biological function have been widely employed as three-dimensional nanobiomaterials for sensitive bioassays, MRI contrast, semiconductor devices, template for hybrid materials, etc., and stable and long-term maintenance of PNPs seems to be of crucial importance. We evaluated the stability of PNPs and the efficacy of lyophilization for the long-term stability of PNPs, especially using green fluorescent protein nanoparticles (gFPNPs) as a model PNP. Fluorescence intensities and TEM images of gFPNPs were analyzed to monitor their functional and structural stabilities. Unlike the green fluorescent protein monomers (eGFP) that were gradually inactivated in aqueous solution, gFPNP in the same aqueous solution retained the initial fluorescence activity and spherical nanoparticle structure even for 2. weeks at 4. °C. To ensure stable and long-term maintenance of gFPNPs, gFPNPs in aqueous solution were converted to the dried solid forms through lyophilization. It is notable that fluorescence activity and nanoparticle structure of gFPNPs that were lyophilized with both Tween 80 and sucrose were very stably maintained even for 10. weeks at various storage temperatures (-20. °C, 4. °C, 25. °C, and 37. °C). During the period of 10. weeks, the fluorescence of gFPNP was always more than 80% level of initial fluorescence at a wide range of temperature. Although this stability study was focused on gFPNPs, the developed optimal lyophilization conditions for gFPNPs can be applied in general to stable and long-term maintenance of many other PNP-derived biomaterials.

AB - Protein nanoparticles (PNPs) that are nanostructured biomaterials with intrinsic biological function have been widely employed as three-dimensional nanobiomaterials for sensitive bioassays, MRI contrast, semiconductor devices, template for hybrid materials, etc., and stable and long-term maintenance of PNPs seems to be of crucial importance. We evaluated the stability of PNPs and the efficacy of lyophilization for the long-term stability of PNPs, especially using green fluorescent protein nanoparticles (gFPNPs) as a model PNP. Fluorescence intensities and TEM images of gFPNPs were analyzed to monitor their functional and structural stabilities. Unlike the green fluorescent protein monomers (eGFP) that were gradually inactivated in aqueous solution, gFPNP in the same aqueous solution retained the initial fluorescence activity and spherical nanoparticle structure even for 2. weeks at 4. °C. To ensure stable and long-term maintenance of gFPNPs, gFPNPs in aqueous solution were converted to the dried solid forms through lyophilization. It is notable that fluorescence activity and nanoparticle structure of gFPNPs that were lyophilized with both Tween 80 and sucrose were very stably maintained even for 10. weeks at various storage temperatures (-20. °C, 4. °C, 25. °C, and 37. °C). During the period of 10. weeks, the fluorescence of gFPNP was always more than 80% level of initial fluorescence at a wide range of temperature. Although this stability study was focused on gFPNPs, the developed optimal lyophilization conditions for gFPNPs can be applied in general to stable and long-term maintenance of many other PNP-derived biomaterials.

KW - Fluorescent protein nanoparticles

KW - Lyophilization

KW - Protein nanoparticle structure

KW - Stability

UR - http://www.scopus.com/inward/record.url?scp=79955663272&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=79955663272&partnerID=8YFLogxK

U2 - 10.1016/j.bbrc.2011.03.123

DO - 10.1016/j.bbrc.2011.03.123

M3 - Article

C2 - 21458416

AN - SCOPUS:79955663272

VL - 408

SP - 225

EP - 229

JO - The BMJ

JF - The BMJ

SN - 0730-6512

IS - 2

ER -