Department of Chemistry, Boston University, Boston, Massachusetts 02215, USA.
Nano Lett. 2011 Feb 9;11(2):498-504. doi: 10.1021/nl103315t. Epub 2011 Jan 19.
The wavelength dependent scattering cross sections of self-assembled silver nanoparticle clusters of known size (n) were measured on five different wavelength channels between 427 and 510 nm through correlation of multispectral imaging and scanning electron microscopy. A multivariate statistical analysis of the spectral response of this training set provided a correlation between spectral response and cluster size and enabled a classification of new measurements into four distinct nanoparticle association levels (I1-I4) whose compositions were dominated by monomers (I1), dimers (I2), trimers and tetramers (I3), and larger clusters (I4), respectively. One potential application of the optical sizing approach is to map association levels of silver immunolabels on cellular surfaces. We demonstrate the feasibility of this approach using silver immunolabels targeted at the epidermal growth factor receptor on A431 cells in a proof of principle experiment. The ability to measure immunolabel association levels on subcellular length scales in an optical microscope provides new opportunities for experimentally assessing receptor density distributions on living cells in solution.
通过多光谱成像和扫描电子显微镜在 427nm 至 510nm 之间的五个不同波长通道上测量了具有已知尺寸(n)的自组装银纳米粒子簇的波长相关散射截面。对该训练集的光谱响应进行多元统计分析,提供了光谱响应与簇尺寸之间的相关性,并能够将新的测量值分为四个不同的纳米粒子缔合水平(I1-I4),其组成分别由单体(I1)、二聚体(I2)、三聚体和四聚体(I3)以及较大的簇(I4)主导。光学尺寸测量方法的一个潜在应用是绘制细胞表面上银免疫标记物的缔合水平。我们使用针对 A431 细胞上表皮生长因子受体的银免疫标记物在原理验证实验中证明了这种方法的可行性。在光学显微镜下测量亚细胞长度尺度上免疫标记物缔合水平的能力为在溶液中评估活细胞上受体密度分布的实验提供了新的机会。