Department of Integrative Structural and Computational Biology and Skaggs Institute of Chemical Biology, The Scripps Research Institute , 10550 North Torrey Pines Road, La Jolla California 92037, United States.
Acc Chem Res. 2017 Jan 17;50(1):105-111. doi: 10.1021/acs.accounts.6b00511. Epub 2016 Dec 29.
Although each type of protein fold and in some cases individual proteins within a fold classification can have very different mechanisms of folding, the underlying biophysical and biochemical principles that operate to cause a linear polypeptide chain to fold into a globular structure must be the same. In an aqueous solution, the protein takes up the thermodynamically most stable structure, but the pathway along which the polypeptide proceeds in order to reach that structure is a function of the amino acid sequence, which must be the final determining factor, not only in shaping the final folded structure, but in dictating the folding pathway. A number of groups have focused on a single protein or group of proteins, to determine in detail the factors that influence the rate and mechanism of folding in a defined system, with the hope that hypothesis-driven experiments can elucidate the underlying principles governing the folding process. Our research group has focused on the folding of the globin family of proteins, and in particular on the monomeric protein apomyoglobin. Apomyoglobin (apoMb) folds relatively slowly (∼2 s) via an ensemble of obligatory intermediates that form rapidly after the initiation of folding. The folding pathway can be dissected using rapid-mixing techniques, which can probe processes in the millisecond time range. Stopped-flow measurements detected by circular dichroism (CD) or fluorescence spectroscopy give information on the rates of folding events. Quench-flow experiments utilize the differential rates of hydrogen-deuterium exchange of amide protons protected in parts of the structure that are folded early; protection of amides can be detected by mass spectrometry or proton nuclear magnetic resonance spectroscopy (NMR). In addition, apoMb forms an intermediate at equilibrium at pH ∼ 4, which is sufficiently stable for it to be structurally characterized by solution methods such as CD, fluorescence and NMR spectroscopies, and the conformational ensembles formed in the presence of denaturing agents and low pH can be characterized as models for the unfolded states of the protein. Newer NMR techniques such as measurement of residual dipolar couplings in the various partly folded states, and relaxation dispersion measurements to probe invisible states present at low concentrations, have contributed to providing a detailed picture of the apomyoglobin folding pathway. The research summarized in this Account was aimed at characterizing and comparing the equilibrium and kinetic intermediates both structurally and dynamically, as well as delineating the complete folding pathway at a residue-specific level, in order to answer the question: "What is it about the amino acid sequence that causes each molecule in the unfolded protein ensemble to start folding, and, once started, to proceed towards the formation of the correctly folded three-dimensional structure?"
尽管每种蛋白质折叠类型,甚至某些折叠分类中的单个蛋白质,都具有非常不同的折叠机制,但导致线性多肽链折叠成球形结构的基本物理化学原理必须相同。在水溶液中,蛋白质呈现热力学上最稳定的结构,但多肽链达到该结构的途径取决于氨基酸序列,这必须是最终的决定性因素,不仅决定最终折叠结构的形状,还决定折叠途径。许多研究小组专注于单个蛋白质或一组蛋白质,以详细确定影响特定系统中折叠速度和机制的因素,希望基于假说的实验能够阐明控制折叠过程的基本原理。我们的研究小组专注于球蛋白家族蛋白质的折叠,特别是单体蛋白质去氧肌红蛋白。去氧肌红蛋白(apoMb)通过快速形成的必需中间产物的整体相对缓慢地折叠(约 2 秒)。使用快速混合技术可以剖析折叠途径,该技术可以探测毫秒级时间范围内的过程。通过圆二色性(CD)或荧光光谱检测到的停流测量值提供有关折叠事件速率的信息。通过氢氘交换的差异速率检测到的快速流动实验利用酰胺质子在结构中较早折叠部分的保护来探测酰胺的保护;可以通过质谱或质子核磁共振波谱法(NMR)检测到酰胺的保护。此外,apoMb 在 pH 值约为 4 时形成平衡中间产物,其足够稳定,可以通过 CD、荧光和 NMR 光谱等溶液方法对其结构进行表征,并且在变性剂和低 pH 值存在下形成的构象集合可以作为蛋白质未折叠状态的模型进行表征。新的 NMR 技术,如在各种部分折叠状态下测量残基偶极耦合,以及测量低浓度下可见状态的弛豫弥散测量,有助于提供 apoMb 折叠途径的详细图像。本研究旨在从结构和动力学两方面对平衡和动力学中间产物进行表征和比较,并在残基特异性水平上描绘完整的折叠途径,以回答以下问题:“是什么导致未折叠蛋白质集合中的每个分子开始折叠,并且一旦开始,就朝着形成正确折叠的三维结构前进?”