Peptide mediated intracellular delivery of semiconductor quantum dots

Anshika Kapur, Malak Safi, Tatiana Domitrovic, Scott H. Medina, Goutam Palui, John E. Johnson, Joel Schneider, Hedi Mattoussi

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Abstract

As control over the growth, stabilization and functionalization of inorganic nanoparticles continue to advance, interest in integrating these materials with biological systems has steadily grown in the past decade. Much attention has been directed towards identifying effective approaches to promote cytosolic internalization of the nanoparticles while avoiding endocytosis. We describe the use of NωV virus derived gamma peptide and a chemically synthesized anticancer peptide, SVS-1 peptide, as vehicles to promote the non-endocytic uptake of luminescent quantum dots (QDs) inside live cells. The gamma peptide is expressed in E. coli as a fusion protein with poly-his tagged MBP (His-MBP-γ) to allow self-assembly onto QDs via metal-histidine conjugation. Conversely, the N-terminal cysteine residue of the SVS-1 peptide is attached to the functionalized QDs via covalent coupling chemistry. Epi-fluorescence microscopy images show that the QD-conjugate staining is distributed throughout the cytoplasm of cell cultures. Additionally, the QD staining does not show co-localization with transferrin-dye-labelled endosomes or DAPI stained nuclei. The QD uptake observed in the presence of physical and pharmacological endocytosis inhibitors further suggest that a physical translocation of QDs through the cell membrane is the driving mechanism for the uptake.

Original languageEnglish (US)
Title of host publicationColloidal Nanoparticles for Biomedical Applications XII
EditorsMarek Osinski, Wolfgang J. Parak, Xing-Jie Liang
PublisherSPIE
ISBN (Electronic)9781510605978
DOIs
StatePublished - Jan 1 2017
EventColloidal Nanoparticles for Biomedical Applications XII 2017 - San Francisco, United States
Duration: Jan 28 2017Jan 31 2017

Publication series

NameProgress in Biomedical Optics and Imaging - Proceedings of SPIE
Volume10078
ISSN (Print)1605-7422

Other

OtherColloidal Nanoparticles for Biomedical Applications XII 2017
CountryUnited States
CitySan Francisco
Period1/28/171/31/17

Fingerprint

Quantum Dots
Semiconductors
Peptides
Semiconductor quantum dots
peptides
delivery
quantum dots
staining
Endocytosis
Nanoparticles
Staining and Labeling
nanoparticles
cytoplasm
histidine
Endosomes
Fluorescence microscopy
cysteine
viruses
Biological systems
Cell membranes

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Atomic and Molecular Physics, and Optics
  • Biomaterials
  • Radiology Nuclear Medicine and imaging

Cite this

Kapur, A., Safi, M., Domitrovic, T., Medina, S. H., Palui, G., Johnson, J. E., ... Mattoussi, H. (2017). Peptide mediated intracellular delivery of semiconductor quantum dots. In M. Osinski, W. J. Parak, & X-J. Liang (Eds.), Colloidal Nanoparticles for Biomedical Applications XII [100780S] (Progress in Biomedical Optics and Imaging - Proceedings of SPIE; Vol. 10078). SPIE. https://doi.org/10.1117/12.2252717
Kapur, Anshika ; Safi, Malak ; Domitrovic, Tatiana ; Medina, Scott H. ; Palui, Goutam ; Johnson, John E. ; Schneider, Joel ; Mattoussi, Hedi. / Peptide mediated intracellular delivery of semiconductor quantum dots. Colloidal Nanoparticles for Biomedical Applications XII. editor / Marek Osinski ; Wolfgang J. Parak ; Xing-Jie Liang. SPIE, 2017. (Progress in Biomedical Optics and Imaging - Proceedings of SPIE).
@inproceedings{bb0203c4ff38458a9061b5a360e1ef56,
title = "Peptide mediated intracellular delivery of semiconductor quantum dots",
abstract = "As control over the growth, stabilization and functionalization of inorganic nanoparticles continue to advance, interest in integrating these materials with biological systems has steadily grown in the past decade. Much attention has been directed towards identifying effective approaches to promote cytosolic internalization of the nanoparticles while avoiding endocytosis. We describe the use of NωV virus derived gamma peptide and a chemically synthesized anticancer peptide, SVS-1 peptide, as vehicles to promote the non-endocytic uptake of luminescent quantum dots (QDs) inside live cells. The gamma peptide is expressed in E. coli as a fusion protein with poly-his tagged MBP (His-MBP-γ) to allow self-assembly onto QDs via metal-histidine conjugation. Conversely, the N-terminal cysteine residue of the SVS-1 peptide is attached to the functionalized QDs via covalent coupling chemistry. Epi-fluorescence microscopy images show that the QD-conjugate staining is distributed throughout the cytoplasm of cell cultures. Additionally, the QD staining does not show co-localization with transferrin-dye-labelled endosomes or DAPI stained nuclei. The QD uptake observed in the presence of physical and pharmacological endocytosis inhibitors further suggest that a physical translocation of QDs through the cell membrane is the driving mechanism for the uptake.",
author = "Anshika Kapur and Malak Safi and Tatiana Domitrovic and Medina, {Scott H.} and Goutam Palui and Johnson, {John E.} and Joel Schneider and Hedi Mattoussi",
year = "2017",
month = "1",
day = "1",
doi = "10.1117/12.2252717",
language = "English (US)",
series = "Progress in Biomedical Optics and Imaging - Proceedings of SPIE",
publisher = "SPIE",
editor = "Marek Osinski and Parak, {Wolfgang J.} and Xing-Jie Liang",
booktitle = "Colloidal Nanoparticles for Biomedical Applications XII",
address = "United States",

}

Kapur, A, Safi, M, Domitrovic, T, Medina, SH, Palui, G, Johnson, JE, Schneider, J & Mattoussi, H 2017, Peptide mediated intracellular delivery of semiconductor quantum dots. in M Osinski, WJ Parak & X-J Liang (eds), Colloidal Nanoparticles for Biomedical Applications XII., 100780S, Progress in Biomedical Optics and Imaging - Proceedings of SPIE, vol. 10078, SPIE, Colloidal Nanoparticles for Biomedical Applications XII 2017, San Francisco, United States, 1/28/17. https://doi.org/10.1117/12.2252717

Peptide mediated intracellular delivery of semiconductor quantum dots. / Kapur, Anshika; Safi, Malak; Domitrovic, Tatiana; Medina, Scott H.; Palui, Goutam; Johnson, John E.; Schneider, Joel; Mattoussi, Hedi.

Colloidal Nanoparticles for Biomedical Applications XII. ed. / Marek Osinski; Wolfgang J. Parak; Xing-Jie Liang. SPIE, 2017. 100780S (Progress in Biomedical Optics and Imaging - Proceedings of SPIE; Vol. 10078).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

TY - GEN

T1 - Peptide mediated intracellular delivery of semiconductor quantum dots

AU - Kapur, Anshika

AU - Safi, Malak

AU - Domitrovic, Tatiana

AU - Medina, Scott H.

AU - Palui, Goutam

AU - Johnson, John E.

AU - Schneider, Joel

AU - Mattoussi, Hedi

PY - 2017/1/1

Y1 - 2017/1/1

N2 - As control over the growth, stabilization and functionalization of inorganic nanoparticles continue to advance, interest in integrating these materials with biological systems has steadily grown in the past decade. Much attention has been directed towards identifying effective approaches to promote cytosolic internalization of the nanoparticles while avoiding endocytosis. We describe the use of NωV virus derived gamma peptide and a chemically synthesized anticancer peptide, SVS-1 peptide, as vehicles to promote the non-endocytic uptake of luminescent quantum dots (QDs) inside live cells. The gamma peptide is expressed in E. coli as a fusion protein with poly-his tagged MBP (His-MBP-γ) to allow self-assembly onto QDs via metal-histidine conjugation. Conversely, the N-terminal cysteine residue of the SVS-1 peptide is attached to the functionalized QDs via covalent coupling chemistry. Epi-fluorescence microscopy images show that the QD-conjugate staining is distributed throughout the cytoplasm of cell cultures. Additionally, the QD staining does not show co-localization with transferrin-dye-labelled endosomes or DAPI stained nuclei. The QD uptake observed in the presence of physical and pharmacological endocytosis inhibitors further suggest that a physical translocation of QDs through the cell membrane is the driving mechanism for the uptake.

AB - As control over the growth, stabilization and functionalization of inorganic nanoparticles continue to advance, interest in integrating these materials with biological systems has steadily grown in the past decade. Much attention has been directed towards identifying effective approaches to promote cytosolic internalization of the nanoparticles while avoiding endocytosis. We describe the use of NωV virus derived gamma peptide and a chemically synthesized anticancer peptide, SVS-1 peptide, as vehicles to promote the non-endocytic uptake of luminescent quantum dots (QDs) inside live cells. The gamma peptide is expressed in E. coli as a fusion protein with poly-his tagged MBP (His-MBP-γ) to allow self-assembly onto QDs via metal-histidine conjugation. Conversely, the N-terminal cysteine residue of the SVS-1 peptide is attached to the functionalized QDs via covalent coupling chemistry. Epi-fluorescence microscopy images show that the QD-conjugate staining is distributed throughout the cytoplasm of cell cultures. Additionally, the QD staining does not show co-localization with transferrin-dye-labelled endosomes or DAPI stained nuclei. The QD uptake observed in the presence of physical and pharmacological endocytosis inhibitors further suggest that a physical translocation of QDs through the cell membrane is the driving mechanism for the uptake.

UR - http://www.scopus.com/inward/record.url?scp=85020165634&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85020165634&partnerID=8YFLogxK

U2 - 10.1117/12.2252717

DO - 10.1117/12.2252717

M3 - Conference contribution

T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE

BT - Colloidal Nanoparticles for Biomedical Applications XII

A2 - Osinski, Marek

A2 - Parak, Wolfgang J.

A2 - Liang, Xing-Jie

PB - SPIE

ER -

Kapur A, Safi M, Domitrovic T, Medina SH, Palui G, Johnson JE et al. Peptide mediated intracellular delivery of semiconductor quantum dots. In Osinski M, Parak WJ, Liang X-J, editors, Colloidal Nanoparticles for Biomedical Applications XII. SPIE. 2017. 100780S. (Progress in Biomedical Optics and Imaging - Proceedings of SPIE). https://doi.org/10.1117/12.2252717