定位产生的何时何地的一般理论与单分子实验相遇
Julius Degünther1, Jann van der Meer1, Udo Seifert1
1II. Institut für Theoretische Physik, Universität Stuttgart, Stuttgart 70550, Germany.
概括
我们在驱动生物物理系统中为粗粒度描述引入波动生产. 这种新概念有助于在部分解决的系统中保留微观过程信息,例如蛋白质展开.
科学领域:
- 生物物理学的生物物理.
- 统计力学 统计力学
- 热力学是一种热力学.
背景情况:
- 随机热力学准确地描述了纳米级生物物理系统.
- 正确的工作关系在完全解决的实验系统中得到验证.
- 部分解决的系统往往被绑定,而不是直接访问,意味着的产生.
研究的目的:
- 在依赖时间的驾驶下,为粗粒度的描述引入波动的产量.
- 将热力学定律的适用性扩展到具有未解决状态的驱动系统.
- 分析部分观察到的生物物理过程中的信息保留.
主要方法:
- 开发了一个波动的生产框架,用于粗粒度描述.
- 将框架应用于蛋白质展开的范式示例.
- 分析了单个轨迹的产生的分布.
主要成果:
- 引入了适用于粗粒度描述中的单个轨迹的波动产量.
- 已证明适用于未解决状态的驱动系统,以蛋白质展开为例.
- 表明粗粒度产生的整个分布保留了微观信息.
结论:
- 波动产量的分布,而不仅仅是平均值,包含空间和时间信息.
- 对于单个展开事件的物理生产分布的边界得到了推导.
- 这一框架增强了对复杂,部分观察到的生物物理系统中的热力学的理解.
相关概念视频
Entropy
29.2K
Salt particles that have dissolved in water never spontaneously come back together in solution to reform solid particles. Moreover, a gas that has expanded in a vacuum remains dispersed and never spontaneously reassembles. The unidirectional nature of these phenomena is the result of a thermodynamic state function called entropy (S). Entropy is the measure of the extent to which the energy is dispersed throughout a system, or in other words, it is proportional to the degree of disorder of a...
29.2K
Entropy within the Cell
10.5K
A living cell's primary tasks of obtaining, transforming, and using energy to do work may seem simple. However, the second law of thermodynamics explains why these tasks are harder than they appear. None of the energy transfers in the universe are completely efficient. In every energy transfer, some amount of energy is lost in a form that is unusable. In most cases, this form is heat energy. Thermodynamically, heat energy is defined as the energy transferred from one system to another that...
10.5K
Protein Dynamics in Living Cells
2.1K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
2.1K


