Urry D W
Laboratory of Molecular Biophysics, University of Alabama, Birmingham 35294.
J Protein Chem. 1988 Feb;7(1):1-34. doi: 10.1007/BF01025411.
Numerous physical characterizations clearly demonstrate that the polypentapeptide of elastin (Val1-Pro2-Gly3-Val4-Gly5)n in water undergoes an inverse temperature transition. Increase in order occurs both intermolecularly and intramolecularly on raising the temperature from 20 to 40 degrees C. The physical characterizations used to demonstrate the inverse temperature transition include microscopy, light scattering, circular dichroism, the nuclear Overhauser effect, temperature dependence of composition, nuclear magnetic resonance (NMR) relaxation, dielectric relaxation, and temperature dependence of elastomer length. At fixed extension of the cross-linked polypentapeptide elastomer, the development of elastomeric force is seen to correlate with increase in intramolecular order, that is, with the inverse temperature transition. Reversible thermal denaturation of the ordered polypentapeptide is observed with composition and circular dichroism studies, and thermal denaturation of the crosslinked elastomer is also observed with loss of elastomeric force and elastic modulus. Thus, elastomeric force is lost when the polypeptide chains are randomized due to heating at high temperature. Clearly, elastomeric force is due to nonrandom polypeptide structure. In spite of this, elastomeric force is demonstrated to be dominantly entropic in origin. The source of the entropic elastomeric force is demonstrated to be the result of internal chain dynamics, and the mechanism is called the librational entropy mechanism of elasticity. There is significant application to the finding that elastomeric force develops due to an inverse temperature transition. By changing the hydrophobicity of the polypeptide, the temperature range for the inverse temperature transition can be changed in a predictable way, and the temperature range for the development of elastomeric force follows. Thus, elastomers have been prepared where the development of elastomeric force is shifted over a 40 degrees C temperature range from a midpoint temperature of 30 degrees C for the polypentapeptide to 10 degrees C by increasing hydrophobicity with addition of a single CH2 moiety per pentamer and to 50 degrees C by decreasing hydrophobicity.(ABSTRACT TRUNCATED AT 400 WORDS)
大量物理表征清楚地表明,弹性蛋白的聚五肽(Val1-Pro2-Gly3-Val4-Gly5)n在水中会发生逆温度转变。从20摄氏度升温至40摄氏度时,分子间和分子内的有序程度均会增加。用于证明逆温度转变的物理表征包括显微镜检查、光散射、圆二色性、核Overhauser效应、组成的温度依赖性、核磁共振(NMR)弛豫、介电弛豫以及弹性体长度的温度依赖性。在交联聚五肽弹性体的固定伸长率下,弹性力的发展与分子内有序程度的增加相关,即与逆温度转变相关。通过组成和圆二色性研究观察到有序聚五肽的可逆热变性,同时也观察到交联弹性体因弹性力和弹性模量的丧失而发生热变性。因此,当多肽链在高温下受热而随机化时,弹性力就会丧失。显然,弹性力源于非随机的多肽结构。尽管如此,弹性力在本质上主要是熵驱动的。熵弹性力的来源被证明是内链动力学的结果,其机制被称为弹性的摆动熵机制。弹性力因逆温度转变而产生这一发现具有重要应用价值。通过改变多肽的疏水性,可以以可预测的方式改变逆温度转变的温度范围,弹性力发展的温度范围也随之改变。因此,已经制备出了弹性体,其中弹性力的发展在40摄氏度的温度范围内发生了变化,从聚五肽的中点温度30摄氏度开始,通过每个五聚体添加一个CH2基团增加疏水性,弹性力发展的中点温度变为10摄氏度,而通过降低疏水性则变为50摄氏度。(摘要截选至400字)