Issue 5, 2020

Lysozyme coated copper nanoclusters for green fluorescence and their utility in cell imaging

Abstract

Fluorescent, pH dependent and water soluble copper nanoclusters (CuNCs) were synthesized using lysozyme (lyz) as the stabilizing agent to give lysozyme coated copper nanoclusters, viz., lyz-CuNCs. The lyz-CuNCs were 3–5 nm in size at neutral pH and exhibit green fluorescence (λem ∼ 510 nm) when excited at 490 nm and exhibited a maximum quantum yield of 18%. However, under basic conditions, aggregates of lyz-CuNCs were seen with a particle size of ∼100 nm. The emission of lyz-CuNCs observed at 510 nm complements that from the blue (λem = 450 nm) and the red (λem = 650 nm) nanoclusters and thus bridges the gap. On the other hand, under acidic conditions, these show a size of 5–10 nm but weakly fluoresce. The particle size and aggregations were monitored by TEM studies carried out using the samples prepared under both the acidic and the basic conditions. The lyz-CuNCs prepared at neutral pH show >90% cell viability and hence can be used as a probe for cellular imaging. The imaging was carried out with both healthy and cancer cell lines, viz., NIH3T3 cells (mouse embryonic fibroblast cell), MCF7 cells (human breast cancer cells) and MDA-MB-231 cells (human estrogen negative breast cancer cells). The Z-stack study suggested the presence of lyz-CuNCs in the cells in cytoplasm. Thus, the green fluorescent lyz-CuNCs can be an alternate to green fluorescent protein (GFP) that is used for cell imaging purposes, since the latter needs a tedious procedure to express, purify and to conjugate.

Graphical abstract: Lysozyme coated copper nanoclusters for green fluorescence and their utility in cell imaging

Article information

Article type
Paper
Submitted
07 Haz 2020
Accepted
11 Tem 2020
First published
14 Tem 2020
This article is Open Access
Creative Commons BY-NC license

Mater. Adv., 2020,1, 1439-1447

Lysozyme coated copper nanoclusters for green fluorescence and their utility in cell imaging

A. G. Thawari, P. Kumar, R. Srivastava and C. P. Rao, Mater. Adv., 2020, 1, 1439 DOI: 10.1039/D0MA00386G

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