Department of Mechanical Engineering, The University of Texas at Dallas 800 West Campbell Rd., Richardson, TX, 75080, USA.
Department of Chemistry and Biochemistry, The University of Texas at Dallas, 800 West Campbell Rd., Richardson, TX, 75080, USA.
Small. 2017 Sep;13(36). doi: 10.1002/smll.201700841. Epub 2017 Jul 11.
Spatiotemporal control of protein structure and activity in biological systems has important and broad implications in biomedical sciences as evidenced by recent advances in optogenetic approaches. Here, this study demonstrates that nanosecond pulsed laser heating of gold nanoparticles (GNP) leads to an ultrahigh and ultrashort temperature increase, coined as "molecular hyperthermia", which causes selective unfolding and inactivation of proteins adjacent to the GNP. Protein inactivation is highly dependent on both laser pulse energy and GNP size, and has a well-defined impact zone in the nanometer scale. It is anticipated that the fine control over protein structure and function enabled by this discovery will be highly enabling within a number of arenas, from probing the biophysics of protein folding/unfolding to the nanoscopic manipulation of biological systems via an optical trigger, to developing novel therapeutics for disease treatment without genetic modification.
在生物系统中对蛋白质结构和活性进行时空控制在生物医学科学中具有重要而广泛的意义,光遗传学方法的最新进展证明了这一点。本研究表明,纳米秒级激光加热金纳米颗粒(GNP)会导致超高和超短的温度升高,被称为“分子热疗”,这会导致与 GNP 相邻的蛋白质选择性展开和失活。蛋白质失活高度依赖于激光脉冲能量和 GNP 尺寸,并且在纳米级范围内具有明确的影响区域。预计,通过这一发现实现的对蛋白质结构和功能的精细控制将在多个领域具有高度的推动作用,从探测蛋白质折叠/展开的生物物理学,到通过光学触发对生物系统进行纳米级操作,再到开发用于疾病治疗的新型疗法而无需基因修饰。