Solid-state electronics and single-molecule biophysics

K. Shepard
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Abstract

Biomolecular systems are traditionally studied using ensemble measurements and fluorescence-based detection. Among the most common in vitro applications are DNA microarrays to identify target gene expression profiles [1] and enzyme-linked immunosorbent assays (ELISA) to identify proteins [2]. While much can be determined with ensemble measurements, scientific and technological interest is rapidly moving to single-molecule techniques. When probing at the single-molecule level, observations can be made about the inter- and intramolecular dynamics that are usually hidden in ensemble measurements. In molecular diagnostic, single-molecule techniques often do not require amplification and simplify sample preparation. The most popular single-molecule techniques based on fluorescence [3, 4] are fundamentally limited in resolution and bandwidth by the countable number of photons emitted by a single fluorophore (typically on the order of 2500 photons/sec). Instrumentation is complex, expensive, and large-form-factor. Furthermore, most optical probes photobleach, limiting observation times and pump powers. Single-molecule measurements of the kinetics of fast biomolecular processes are often unavailable through fluorescent techniques, as they lack the required temporal resolution.
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固态电子学和单分子生物物理学
生物分子系统传统上使用集合测量和基于荧光的检测来研究。最常见的体外应用是DNA微阵列鉴定靶基因表达谱[1]和酶联免疫吸附试验(ELISA)鉴定蛋白质[2]。虽然集合测量可以确定很多东西,但科学和技术的兴趣正迅速转向单分子技术。在单分子水平上进行探测时,可以观察到通常隐藏在系综测量中的分子间和分子内动力学。在分子诊断中,单分子技术通常不需要扩增和简化样品制备。最流行的基于荧光的单分子技术[3,4]在分辨率和带宽上受到单个荧光团发射的光子数量的限制(通常在2500光子/秒的数量级上)。仪器复杂、昂贵且尺寸大。此外,大多数光学探针会发生光漂白,限制了观察时间和泵浦功率。快速生物分子过程动力学的单分子测量通常无法通过荧光技术实现,因为它们缺乏所需的时间分辨率。
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