Functionalization of II-VI semiconductor quantum Dots with peptides and integrins of cancer cells for biophotonic applications

Nanoscale functionalization of semiconductor quantum dots (SQDs) with biomedical structures is promising for many applications and novel studies of intrinsic properties of both constituent systems. The use of SQDs as biotags has emphasized use of the semiconductor luminescence to determine the l...

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Autores principales: Bairamov, B., Toporov, V., Bairamov, F., Lanzov, V., Petuhov, M., Glazunov, E., Li, Yang, Ramadurai, Dinakar, Peng, Sh., Dutta, Mitra, Stroscio, M., Irmer, Gert
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Publicado: D.Ghitu Institute of Electronic Engineering and Nanotechnologies 2006
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spelling oai:doaj.org-article:e2e31697d2094c058ca25dceccb5c54e2021-11-21T12:09:02ZFunctionalization of II-VI semiconductor quantum Dots with peptides and integrins of cancer cells for biophotonic applications2537-63651810-648Xhttps://doaj.org/article/e2e31697d2094c058ca25dceccb5c54e2006-12-01T00:00:00Zhttps://mjps.nanotech.md/archive/2006/article/3560https://doaj.org/toc/1810-648Xhttps://doaj.org/toc/2537-6365Nanoscale functionalization of semiconductor quantum dots (SQDs) with biomedical structures is promising for many applications and novel studies of intrinsic properties of both constituent systems. The use of SQDs as biotags has emphasized use of the semiconductor luminescence to determine the location where chemically functionalized SQDs bind to a biomedical sample. We study chemically prepared CdS SQDs functionalized with peptides composed of the following amino acid chains: CGGGRGDS, CGGGRVDS, CGGIKVAV, and CGGGLDV. We find that the effective diameter of the CdS SQDs is 3 nm. As will be seen the cysteine (C) amino acid links to CdS SQDs via the thiol link, the GGG sequences of glycine (G) amino acid, provide a spacer in the amino acid chain. At the same time the RGDS, RVDS, IKAV, and LDV sequences have selective bonding affinities to specialized transmembrane cellular structures known as integrins of neurons and MDA-MB-435 cancer cells, respectively. Since protein hydration is known to be a key factor affecting protein energy balance, we also studied a role that water and other bioenvironments may play in stability, surface properties, dynamical and structural characteristics of these systems. We found the roles that the quantum confinement and functionalizing in biomedical environments play in altering and determining the electronic, optical, and vibrational properties of these nanostructures as well as demonstrated the effectiveness of CdS SQD use as integrin sensitive biotags. Bairamov, B.Toporov, V.Bairamov, F.Lanzov, V.Petuhov, M.Glazunov, E.Li, YangRamadurai, DinakarPeng, Sh.Dutta, MitraStroscio, M.Irmer, GertD.Ghitu Institute of Electronic Engineering and NanotechnologiesarticlePhysicsQC1-999ElectronicsTK7800-8360ENMoldavian Journal of the Physical Sciences, Vol 5, Iss 3-4, Pp 320-326 (2006)
institution DOAJ
collection DOAJ
language EN
topic Physics
QC1-999
Electronics
TK7800-8360
spellingShingle Physics
QC1-999
Electronics
TK7800-8360
Bairamov, B.
Toporov, V.
Bairamov, F.
Lanzov, V.
Petuhov, M.
Glazunov, E.
Li, Yang
Ramadurai, Dinakar
Peng, Sh.
Dutta, Mitra
Stroscio, M.
Irmer, Gert
Functionalization of II-VI semiconductor quantum Dots with peptides and integrins of cancer cells for biophotonic applications
description Nanoscale functionalization of semiconductor quantum dots (SQDs) with biomedical structures is promising for many applications and novel studies of intrinsic properties of both constituent systems. The use of SQDs as biotags has emphasized use of the semiconductor luminescence to determine the location where chemically functionalized SQDs bind to a biomedical sample. We study chemically prepared CdS SQDs functionalized with peptides composed of the following amino acid chains: CGGGRGDS, CGGGRVDS, CGGIKVAV, and CGGGLDV. We find that the effective diameter of the CdS SQDs is 3 nm. As will be seen the cysteine (C) amino acid links to CdS SQDs via the thiol link, the GGG sequences of glycine (G) amino acid, provide a spacer in the amino acid chain. At the same time the RGDS, RVDS, IKAV, and LDV sequences have selective bonding affinities to specialized transmembrane cellular structures known as integrins of neurons and MDA-MB-435 cancer cells, respectively. Since protein hydration is known to be a key factor affecting protein energy balance, we also studied a role that water and other bioenvironments may play in stability, surface properties, dynamical and structural characteristics of these systems. We found the roles that the quantum confinement and functionalizing in biomedical environments play in altering and determining the electronic, optical, and vibrational properties of these nanostructures as well as demonstrated the effectiveness of CdS SQD use as integrin sensitive biotags.
format article
author Bairamov, B.
Toporov, V.
Bairamov, F.
Lanzov, V.
Petuhov, M.
Glazunov, E.
Li, Yang
Ramadurai, Dinakar
Peng, Sh.
Dutta, Mitra
Stroscio, M.
Irmer, Gert
author_facet Bairamov, B.
Toporov, V.
Bairamov, F.
Lanzov, V.
Petuhov, M.
Glazunov, E.
Li, Yang
Ramadurai, Dinakar
Peng, Sh.
Dutta, Mitra
Stroscio, M.
Irmer, Gert
author_sort Bairamov, B.
title Functionalization of II-VI semiconductor quantum Dots with peptides and integrins of cancer cells for biophotonic applications
title_short Functionalization of II-VI semiconductor quantum Dots with peptides and integrins of cancer cells for biophotonic applications
title_full Functionalization of II-VI semiconductor quantum Dots with peptides and integrins of cancer cells for biophotonic applications
title_fullStr Functionalization of II-VI semiconductor quantum Dots with peptides and integrins of cancer cells for biophotonic applications
title_full_unstemmed Functionalization of II-VI semiconductor quantum Dots with peptides and integrins of cancer cells for biophotonic applications
title_sort functionalization of ii-vi semiconductor quantum dots with peptides and integrins of cancer cells for biophotonic applications
publisher D.Ghitu Institute of Electronic Engineering and Nanotechnologies
publishDate 2006
url https://doaj.org/article/e2e31697d2094c058ca25dceccb5c54e
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