Label-free free-solution nanoaperture optical tweezers for single molecule protein studies

被引:79
作者
Al Balushi, Ahmed A. [1 ]
Kotnala, Abhay [1 ]
Wheaton, Skyler [1 ]
Gelfand, Ryan M. [1 ]
Rajashekara, Yashaswini [1 ]
Gordon, Reuven [1 ]
机构
[1] Univ Victoria, Dept Elect & Comp Engn, Victoria, BC V8P 5C2, Canada
关键词
ENHANCED RAMAN-SPECTROSCOPY; SURFACE-PLASMON RESONANCE; DOUBLE-HOLE ARRAYS; GOLD NANOPARTICLES; MICROFLUIDIC SYSTEMS; NANO-TWEEZER; BINDING; MANIPULATION; FORCE; LIGHT;
D O I
10.1039/c4an02213k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Nanoaperture optical tweezers are emerging as useful label-free, free-solution tools for the detection and identification of biological molecules and their interactions at the single molecule level. Nanoaperture optical tweezers provide a low-cost, scalable, straight-forward, high-speed and highly sensitive (SNR similar to 33) platform to observe real-time dynamics and to quantify binding kinetics of protein-small molecule interactions without the need to use tethers or labeling. Such nanoaperture-based optical tweezers, which are 1000 times more efficient than conventional optical tweezers, have been used to trap and isolate single DNA molecules and to study proteins like p53, which has been claimed to be in mutant form for 75% of human cancers. More recently, nanoaperture optical tweezers have been used to probe the low-frequency (in the single digit wavenumber range) Raman active modes of single nanoparticles and proteins. Here we review recent developments in the field of nanoaperture optical tweezers and how they have been applied to protein-antibody interactions, protein-small molecule interactions including single molecule binding kinetics, and protein-DNA interactions. In addition, recent works on the integration of nanoaperture optical tweezers at the tip of optical fiber and in microfluidic environments are presented.
引用
收藏
页码:4760 / 4778
页数:19
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