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蛋白质折叠的热力学:水合作用和静电相互作用的影响。

Thermodynamics of protein folding: effects of hydration and electrostatic interactions.

作者信息

Ooi T

机构信息

Department of Food Sciences, Kyoto Women's University, Japan.

出版信息

Adv Biophys. 1994;30:105-54. doi: 10.1016/0065-227x(94)90012-4.

Abstract

DNA base sequences contain a variety of information, and this information flows from DNA to a protein through the steps of transcription and translation. The one dimensional information given from DNA is the amino acid sequence of the protein. In an organism, a nascent chain synthesized in vivo from the N-terminus according to the information in DNA folds spontaneously to a native conformation under a given environmental condition, i.e., water is the solvent and concentration of salts, pH, temperature, and pressure are appropriate. The polypeptide chain synthesized chemically from the C-terminus also folds to the native conformation, and often exhibits the proper enzymic activity. X-ray crystallography reveals the three dimensional structure of a protein in crystal, indicating that the location of the constituent atoms in the space is specific for that protein, i.e., the information on how to fold is contained in the amino acid sequence. In order to understand the folding, however, other factors such as geometrical information on each amino acid should be taken into account, because a sequence is one dimensional information and a 3D structure is three dimensional. Environmental conditions are also crucial factors in the folding, since a change in conditions can destroy the native structure. The folding and unfolding phenomena are described in terms of thermodynamics when the processes occur reversibly. As experiments show, the stability of a protein conformation can be described by the free energy of folding or unfolding. Folding of a nascent chain to the native conformation, thus, is interpreted as the process towards a minimum of the folding free energy. Thermodynamic quantities of folding or unfolding are expressed as functions of temperature, pressure, and concentration of reagents such as salts, and the quantities are measured as the differences between states, e.g., the N and D states. Since the effects of surrounding media must be included, the phenomenon in aqueous solution at a given condition of pH and salt concentration is divided into the several steps shown in Fig. 12. The chain molecule has two states, N and D, in vacuo; the molecule is then transferred into water, accompanied by the hydration in both states; next, the ionization process produces electrostatic interactions in the molecule; and finally, addition of chemical reagents like denaturants has other effects on the stability.

摘要

DNA碱基序列包含多种信息,这些信息通过转录和翻译步骤从DNA流向蛋白质。DNA给出的一维信息是蛋白质的氨基酸序列。在生物体中,根据DNA中的信息在体内从N端合成的新生链在给定的环境条件下(即水为溶剂且盐浓度、pH值、温度和压力适宜)会自发折叠成天然构象。从C端化学合成的多肽链也会折叠成天然构象,并且常常表现出适当的酶活性。X射线晶体学揭示了晶体中蛋白质的三维结构,表明空间中组成原子的位置对于该蛋白质是特定的,即折叠方式的信息包含在氨基酸序列中。然而,为了理解折叠过程,还应考虑其他因素,如每个氨基酸的几何信息,因为序列是一维信息而三维结构是三维的。环境条件也是折叠过程中的关键因素,因为条件的变化可能会破坏天然结构。当过程可逆发生时,折叠和去折叠现象用热力学来描述。如实验所示,蛋白质构象的稳定性可用折叠或去折叠的自由能来描述。因此,新生链折叠成天然构象被解释为朝着折叠自由能最小化的过程。折叠或去折叠的热力学量表示为温度、压力和盐等试剂浓度的函数,并且这些量作为状态之间的差异来测量,例如N态和D态之间的差异。由于必须考虑周围介质的影响,在给定pH值和盐浓度条件下的水溶液中的现象可分为图12所示的几个步骤。链分子在真空中有N和D两种状态;然后分子转移到水中,两种状态都会发生水合作用;接下来,电离过程在分子中产生静电相互作用;最后,加入变性剂等化学试剂会对稳定性产生其他影响。

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