Molecular Biophysics Unit, Indian Institute of Science, Bangalore 560 012, India.
Proteins. 2010 Apr;78(5):1228-42. doi: 10.1002/prot.22641.
To understand structural and thermodynamic features of disulfides within an alpha-helix, a non-redundant dataset comprising of 5025 polypeptide chains containing 2311 disulfides was examined. Thirty-five examples were found of intrahelical disulfides involving a CXXC motif between the N-Cap and third helical positions. GLY and PRO were the most common amino acids at positions 1 and 2, respectively. The N-Cap residue for disulfide bonded CXXC motifs had average (phi,psi) values of (-112 +/- 25.2 degrees , 106 +/- 25.4 degrees ). To further explore conformational requirements for intrahelical disulfides, CYS pairs were introduced at positions N-Cap-3; 1,4; 7,10 in two helices of an Escherichia coli thioredoxin mutant lacking its active site disulfide (nSS Trx). In both helices, disulfides formed spontaneously during purification only at positions N-Cap-3. Mutant stabilities were characterized by chemical denaturation studies (in both oxidized and reduced states) and differential scanning calorimetry (oxidized state only). All oxidized as well as reduced mutants were destabilized relative to nSS Trx. All mutants were redox active, but showed decreased activity relative to wild-type thioredoxin. Such engineered disulfides can be used to probe helix start sites in proteins of unknown structure and to introduce redox activity into proteins. Conversely, a protein with CYS residues at positions N-Cap and 3 of an alpha-helix is likely to have redox activity.
为了了解α-螺旋中二硫键的结构和热力学特征,研究了一个由 5025 条多肽链组成的非冗余数据集,其中包含 2311 个二硫键。发现了 35 个涉及 N-端和第三螺旋位置之间CXXC 模体的螺旋内二硫键的例子。GLY 和 PRO 分别是位置 1 和 2 最常见的氨基酸。二硫键结合的 CXXC 模体的 N-端残基的平均(phi,psi)值为(-112 +/- 25.2 度,106 +/- 25.4 度)。为了进一步探索螺旋内二硫键的构象要求,在一个缺乏活性位点二硫键的大肠杆菌硫氧还蛋白突变体的两条螺旋中,将 CYS 对引入 N-端-3 位;1,4;7,10。在两条螺旋中,只有在 N-端-3 位,二硫键才能在纯化过程中自发形成。通过化学变性研究(氧化和还原状态)和差示扫描量热法(仅氧化状态)来表征突变体的稳定性。与 nSS Trx 相比,所有氧化和还原突变体都不稳定。所有突变体都是氧化还原活性的,但与野生型硫氧还蛋白相比,活性降低。这种工程化的二硫键可用于探测未知结构蛋白的螺旋起始位点,并向蛋白中引入氧化还原活性。相反,在α-螺旋的 N-端和 3 位具有 CYS 残基的蛋白质很可能具有氧化还原活性。