动态可以驱动酶的冷适应
Harry G Saavedra1,2, James O Wrabl1,2, Jeremy A Anderson1,2
1Department of Biology, Johns Hopkins University, Baltimore, MD, USA.
Nature
|June 8, 2018
概括
生物通过酶的进化变化适应新环境. 这项研究揭示了远距离突变如何调整酶活性,影响基质亲和率和循环率,而不会改变活性部位结构.
科学领域:
- 进化生物学
- 生物化学
- 酶动力学
背景情况:
- 生物通过进化变化适应环境的特殊环境,例如极端温度.
- 来自不同环境的酶基因表现出保持催化速率的适应性突变.
- 适应性突变通常发生在远离酶活性部位的表面部位,这就提出了关于全调节的问题.
研究的目的:
- 研究酶动力学在全调节和适应中的作用.
- 探索远端序列的变化如何调节酶活性.
- 了解酶在进化过程中的微调功能机制.
主要方法:
- 工程调突变进入大肠杆菌基酶的远端部位.
- 量化评估这些突变对酶动力学,基质亲和和和循环率的影响.
- 分析控制关键酶参数的空间分离.
主要成果:
- 一个基于动态的全调节机制被揭示出来.
- 在LID域控制基质亲和度的波动.
- 在AMP结合领域的动态衰减影响了酶的循环.
- 在酶参数的控制中发现了空间分离.
结论:
- 酶适应可以通过基于动态的全调节来实现,在不改变基本状态结构的情况下改变功能.
- 这种机制为了解酶动态与营业额之间的关系提供了一个新的模型.
- 基于动态的调节是生物功能微调的潜在广泛的进化策略.
相关概念视频
Responses to Heat and Cold Stress
14.9K
Every organism has an optimum temperature range within which healthy growth and physiological functioning can occur. At the ends of this range, there will be a minimum and maximum temperature that interrupt biological processes.
14.9K
Enzymes
95.0K
Inside living organisms, enzymes act as catalysts for many biochemical reactions involved in cellular metabolism. The role of enzymes is to reduce the activation energies of biochemical reactions by forming complexes with its substrates. The lowering of activation energies favor an increase in the rates of biochemical reactions.
Enzyme deficiencies can often translate into life-threatening diseases. For example, a genetic abnormality resulting in the deficiency of the enzyme G6PD...
Enzyme deficiencies can often translate into life-threatening diseases. For example, a genetic abnormality resulting in the deficiency of the enzyme G6PD...
95.0K
Enzyme Kinetics
104.2K
Enzymes speed up reactions by lowering the activation energy of the reactants. The speed at which the enzyme turns reactants into products is called the rate of reaction. Several factors impact the rate of reaction, including the number of available reactants. Enzyme kinetics is the study of how an enzyme changes the rate of a reaction.
Scientists typically study enzyme kinetics with a fixed amount of enzyme in the controlled environment of a test tube. When more reactant, or substrate, is...
Scientists typically study enzyme kinetics with a fixed amount of enzyme in the controlled environment of a test tube. When more reactant, or substrate, is...
104.2K
Energy to Drive Translocation
2.9K
Mitochondrial protein import is powered by two distinct energy sources: ATP hydrolysis and electrochemical potential across the inner membrane. Newly synthesized precursors are bound by cytosolic chaperones of the Hsp70 family, which guide them to the import receptors on the mitochondrial surface. Utilizing the energy of ATP hydrolysis, Hsp70 chaperones transfer these precursors to the TOM receptors on the mitochondrial outer membrane.
Generally, polypeptides are unfolded by two distinct...
Generally, polypeptides are unfolded by two distinct...
2.9K
Cold Weather Concreting
387
When freshly poured concrete is exposed to freezing temperatures before it has set, the water within the concrete can freeze. This expansion disrupts the setting process, delays chemical reactions necessary for hardening, and increases the volume of pores within the hardened concrete, which weakens its overall structure. If the concrete manages to reach an appreciable strength before it freezes, the damage can be somewhat mitigated.
To counteract the negative impacts of cold weather, ensuring...
To counteract the negative impacts of cold weather, ensuring...
387
M-Cdk Drives Transition Into Mitosis
6.6K
Checkpoints throughout the cell cycle serve as safeguards and gatekeepers, allowing the cell cycle to progress in favorable conditions and slow or halt it in problematic ones. This regulation is known as the cell cycle control system.
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
6.6K


