带羟乙基侧臂三脚架多胺Cu(Ⅱ)配合物切割肌红蛋白所得片断的质谱指认

采用电喷雾质谱和串联质谱以及聚丙烯酰胺凝胶电泳技术研究了[CuL(H₂O)](BF₄)₂(L为2-[二(2-氨乙酸)氨基]乙醇)与马心肌红蛋白的键合作用和水解切割。聚丙烯酰胺凝胶电泳研究显示在中性及60 ℃条件下，切割效率与[CuL(H₂O)]²⁺的浓度和温育时间密切相关。电喷雾质谱和串联质谱分析显示，[CuL(H₂O)]²⁺通过与肌红蛋白的氨基酸His36，His93，His116和Arg139侧链的结合，并在羟乙基侧臂的促进下，选择性地水解了肽键Phe33-Thr34，Gln91-Ser92，Ala94-Thr95，His116-Ser117和Asn140-Asp141。     

CrOx/SiO2催化剂上丙烷在CO2气氛中脱氢反应的研究

采用XRD、UV-vis DRS、ESR和微分吸附量热等技术,考察了铬担载量分别为2.5、5和10wt%的CrO_x/SiO₂催化剂的结构、表面性质和氧化还原性能。结果表明,催化剂表面上存在多种Cr的氧化态和聚集形式。随着Cr担载量从2.5wt%到10wt%的逐渐增大,催化剂表面占主导地位的Cr物种由CrO₃单体转为多聚CrO₃和Cr₂O₃晶相。在CO₂气氛中催化剂对丙烷转化率和丙烯选择性的大小顺序为2.5wt%CrO_x/SiO₂>5wt%CrO_x/SiO₂>10wt%CrO_x/SiO₂,反应过程中的原位ESR和UV-visDRS测定结果表明,催化剂表面的反应活性中心为Cr⁵⁺,Cr⁵⁺可由催化剂预处理过程中Cr³⁺的氧化及丙烷反应过程中CrO₃单体的还原产生,在反应中CO₂可使Cr³⁺重新氧化为Cr⁵⁺.     

离子色谱法测定水体中化学需氧量的研究

本文提出了一种将离子色谱和纳米TiO₂－K₂S₂O₈共存体系相结合测定水体中化学需氧量（COD）值的新方法。其测定原理是基于纳米TiO₂ –K₂S₂O₈共存体系对有机物的光催化氧化，体系降解有机物产生的SO₄^2-，利用离子色谱电导检测法测定SO₄^2-的浓度，其电导率响应值的变化量与水体中化学需氧量呈一定的比例关系。本文研究了测定机理，优化了测定条件，结果表明，本方法操作条件温和，能实现快速、准确的测定。COD值在10.0～300.0mg·L^-1浓度范围内，与电导信号值成线性关系，以三倍信噪比计算检测限为3.3mg·L^-1。将本方法用于实际水样的检测，测定结果与COD标准分析法有好的一致性。     

298.15 K Li2B4O7-MgCl2-H2O体系热力学性质的电动势法测定及离子相互作用模型的研究

测定了298.15 K下, 无液接电池Li-ISE│Li₂B₄O₇ (m_A)(aq.), MgCl₂(m_B)(aq.)│AgCl/Ag的电动势, 利用测定结果计算了Li₂B₄O₇-MgCl₂-H₂O体系离子强度在0.05～3 mol•kg^－1范围内, 不同MgCl₂离子强度分数的溶液中LiCl的平均活度系数, 并给出了其随离子强度I, B₄O₇^2－和Mg^2＋浓度的变化规律. 结合以往关于该体系和Li₂B₄O₇-LiCl-H₂O, Li₂B₄O₇-H₂O体系的等压研究结果, 用迭代和多元线性回归方法对Li^＋-Mg^2＋-Cl^－-B₄O₇^2－-H₂O体系的离子相互作用模型进行了研究. 具体方法为考虑了该体系在不同的总硼浓度范围H₃BO₃, B(OH)₄^－, B₃O₃(OH)₄^－和B₄O₅(OH)₄^2－四种含硼化合物的存在以及各硼化合物间的化学平衡, 以修正了的Pitzer渗透系数方程和活度系数方程为基础, 对该体系的等压法和电动势法研究结果进行最小二乘拟合, 拟合的标准偏差为0.0167, 用该模型计算的该体系的渗透系数、活度系数与实验值基本一致.     

Ni2+在γ-Al2O3上的分散状态及负载型Ni/γ-Al2O3催化剂的α-蒎烯加氢活性

用X-射线衍射(XRD)、紫外-可见漫散射光谱(UV-Vis DRS)、程序升温还原(TPR)、CO化学吸附和微反测试等方法研究了Ni²⁺在γ-Al₂O₃上的分散状态和负载型Ni/γ-Al₂O₃催化剂的α-蒎烯加氢催化活性。结果表明，当Ni²⁺负载量远低于其在γ-Al₂O₃载体表面分散容量时，Ni²⁺优先嵌入载体表面四面体空位，随着Ni²⁺负载量的增加，嵌入载体表面八面体空位Ni²⁺的比例增大。由于八面体Ni²⁺易被还原为金属态Ni⁰，NiO/γ-Al₂O₃样品的还原度随Ni²⁺负载量的增加而大幅度地增加，经氢还原所得Ni/γ-Al₂O₃催化剂的CO吸附量和α-蒎烯加氢催化活性大幅度增加。对La₂O₃助剂的作用进行了研究，结果表明分散在γ-Al₂O₃上的La³⁺物种可阻止Ni²⁺嵌入γ-Al₂O₃表面四面体空位，增大了八面体Ni²⁺物种所占比例，提高了催化剂的还原度，故Ni-La₂O₃/γ-Al₂O₃催化剂催化活性高于Ni/γ-Al₂O₃催化剂。     

298.15 K Li2B4O7-MgCl2-H2O体系热力学性质的电动势法测定及离子相互作用模型的研究

测定了298.15 K下, 无液接电池Li-ISE│Li₂B₄O₇ (m_A)(aq.), MgCl₂(m_B)(aq.)│AgCl/Ag的电动势, 利用测定结果计算了Li₂B₄O₇-MgCl₂-H₂O体系离子强度在0.05～3 mol•kg^－1范围内, 不同MgCl₂离子强度分数的溶液中LiCl的平均活度系数, 并给出了其随离子强度I, B₄O₇^2－和Mg^2＋浓度的变化规律. 结合以往关于该体系和Li₂B₄O₇-LiCl-H₂O, Li₂B₄O₇-H₂O体系的等压研究结果, 用迭代和多元线性回归方法对Li^＋-Mg^2＋-Cl^－-B₄O₇^2－-H₂O体系的离子相互作用模型进行了研究. 具体方法为考虑了该体系在不同的总硼浓度范围H₃BO₃, B(OH)₄^－, B₃O₃(OH)₄^－和B₄O₅(OH)₄^2－四种含硼化合物的存在以及各硼化合物间的化学平衡, 以修正了的Pitzer渗透系数方程和活度系数方程为基础, 对该体系的等压法和电动势法研究结果进行最小二乘拟合, 拟合的标准偏差为0.0167, 用该模型计算的该体系的渗透系数、活度系数与实验值基本一致.     

HO2自由基与NO2反应通道的理论研究

应用密度泛函理论DFT/B3LYP对HO₂＋NO₂反应进行了研究, 在B3LYP/6-311G^**和CCSD(T)/6-311G^**水平上计算了HO₂自由基与NO₂分子反应的单重态和三重态反应势能面, 计算结果表明, 单重态反应势能面中的直接氢抽提反应机理是此反应的主要反应通道, 即HO₂自由基的氢原子转移到NO₂分子的氮原子上形成产物P₁ (HNO₂＋³O₂), 另一个可能的反应通道是单重态反应势能面上HO₂中的端位氧原子进攻NO₂分子中的氮原子形成中间体1 (HOONO₂), 接着中间体1 (HOONO₂)经过氢转移形成产物P₂ (trans-HONO＋³O₂), 以上两个反应通道都是放热反应通道, 分别放热90.14和132.52 kJ•mol^－1.     

V2O5-TiO2复合半导体光催化材料结构及光响应性能研究

采用溶胶凝胶法制备了V₂O₅-TiO₂复合半导体材料，通过Raman、XRD及UV-Vis DRS等实验方法研究了V₂O₅与TiO₂复合对材料表面组成、晶体结构以及光响应性能的影响。结果表明：钒加入后优先与TiO₂作用形成较为稳定的金红石型TiVO₄晶相，其中V⁴⁺是促进TiO₂发生相变的关键；随着钒加入量的增加，V₂O₅由表面高分散状态逐渐聚集形成晶相，并释放部分Ti⁴⁺使之形成锐钛矿型TiO₂晶相，使得体相中金红石型TiO₂的含量有所下降；复合后形成的TiVO₄晶相显著提高了材料对可见光的吸收率，并使其吸光域红移至460 nm左右。     

Fe2O3/Al2O3二元气凝胶合成高质量单壁纳米碳管

通过溶胶和超临界干燥方法制得了Fe₂O₃/Al₂O₃二元气凝胶，其比表面积和孔隙体积分别为246 m²·g^-1和1.89 cm³·g^-1，并具有较宽的孔径分布。以Fe₂O₃/Al₂O₃二元气凝胶作催化剂，通过甲烷催化裂解成功地合成了高质量的单壁纳米碳管。利用FESEM、TEM和HRTEM、Raman光谱等分析手段研究了反应温度对单壁纳米碳管生长的影响。结果表明在900 ℃时合成单壁纳米碳管的质量较高，并且合成的炭产物为毡状，该炭产物主要为高质量的单壁纳米碳管。     

H2SO4处理的Nb2O5/γ -Al2O3催化剂表面酸性与催化性能研究

用Hammett指示剂法、红外光谱（IR）、示差扫描量热-热重法（DSC-TG）和微型催化反应装置等研究了H₂SO₄处理的负载型Nb₂O₅/γ-Al₂O₃催化剂表面酸性和催化异丁烯（IB）与异丁醛（IBA）反应生成2，5-二甲基-2，4-己二烯（DMHD）的催化性能。结果表明随所用H₂SO₄浓度增加，Nb₂O₅/γ-Al₂O₃催化剂表面酸性增强，B酸量增加，L酸量先增加后下降。经H₂SO₄处理的Nb₂O₅/γ-Al₂O₃催化剂的催化活性明显增加，但当H₂SO₄浓度超过0.05 mol·L^-1时催化活性又急剧下降，这可能是因为在H₂SO₄处理的催化剂表面形成的强酸中心上，产物分子进一步转化为积炭且封闭催化剂活性表面，导致催化活性下降。     

Mass spectrometry assisted assignments of binding and cleavage sites of Zn(Ⅱ)complex towards oxidized insulin B chain

The electrospray ionization mass spectrometry investigation showed that the binding sites of [ZnL]2+, where L is 2-[bis(2-aminoethyl)aminolethanol, with oxidized insulin B chain are Phe1, His5 and Arg22, which lead to the selective cleavages of the peptide bonds at Phe1-Val2, His5-Leu6, Glu21-Arg22, and Arg22-Gly23 of oxidized insulin B chain.     

Site-specifically cleavage of oxidized insulin B chain with Zn（Ⅱ） ion studied by electrospray ionization mass spectrometry

The electrospray ionization mass spectrometry and tandem mass spectrometry investigation showed that the binding sites of Zn^2＋ with oxidized insulin B chain are His 5, His 10, and Arg 22, which lead to the selective cleavages of the peptide bonds at Ash 3- Gin 4, His 5-Leu 6, Gly 8-Ser 9, and Glu 21-Arg 22 of oxidized insulin B chain.     

Mass spectrometry assisted assignments of binding and cleavage sites of copper(II) and platinum(II) complexes towards oxidized insulin B chain

Interaction of cis-[Pt(en)(H2O)2]2+ and [CuL(H2O)]2+, where L is 2-[bis(2-aminoethyl)amino]ethanol, with oxidized insulin B chain in molar ratio of 1 : 1, 1 : 2 and 1 : 3 at pH 2.5 and 40 degrees C has been investigated by electrospray ionization mass spectrometry (ESI-MS) and tandem mass spectrometry (MS/MS). The results show that the binding sites of the two complexes with oxidized insulin B chain are terminal NH2, imidazole groups of His5 and His10. The hydrolytic cleavage studies show that the [CuL(H2O)]2+, upon a pendant hydroxyl group of the ligand, selectively cleaves the peptide bonds at Gly8-Ser9, Asn3-Gln4 and Phe1-Val2, and the cis-[Pt(en)(H2O)2]2+ only cleaves the peptide bond at His10-Leu11. This is the first report of cis-[Pt(en)(H2O)2]2+-promoted cleavage of His-X peptide bond.     

Site-specifically Hydrolytic Cleavage of Oxidized Insulin B Chain With Cu(II) Ion

Selectively chemical cleavage of peptides and proteins is one of the most important reactions in both chemical and biochemical processes. Over the past decade, the interaction of palladium(II) complexes with methionine, cysteine and histidine-containing peptides and proteins and the hydrolytic cleavage of the corresponding amide bond by Pd(II) complexes have been extensively studied1-13. However, reports concerning the directly selective hydrolysis of peptides and proteins with other simple …     

Binding sites of [Ru(bpy)2(H2O)2](BF4)2 with sulfur- and histidine-containing peptides studied by electrospray ionization mass spectrometry and tandem mass spectrometry

The composition and binding sites of cis-[Ru(II)(bpy)2]2+-bound sulfur-containing peptides of Met-Arg-Phe-Ala, glutathione and oxidized glutathione, and also histidine-containing peptide of oxidized insulin B chain, were investigated by electrospray ionization mass spectrometry (ESI-MS) and tandem mass spectrometry (MS/MS). The composition of Ru(II)-containing peptides was precisely determined by ESI-MS, zoom scan and simulation of isotope distribution patterns. MS/MS analysis shows that, in sulfur-containing peptides, the Ru(II) complex prefers to anchor to a carboxyl group, although some other potential binding sites of thiol, thioether and N-terminal amino groups present in these peptides, and in oxidized insulin B chain, Ru(II) first anchors to His10, then either to the hydroxyl group of Thr27 or to the carboxyl group of Ala30. Its secondary structure and microenvironment surrounding the potential binding sites may affect the binding ability of cis-[Ru(II)(bpy)2]2+ to oxidized insulin B chain.     

Effects of cysteic acid groups on the gas-phase reactivity and dissociation of [M + 4H]4+ ions from insulin chain B

Gas-phase ion/molecule reactions and collision-induced dissociation (CID) were conducted on [M + 4H]4+ of insulin chain B. This Fourier transform mass spectrometry work involved ions from the oxidized peptide (with two cysteic acid residues) and its reduced form (with two cysteine residues). Kinetic behavior during deprotonation and hydrogen/deuterium exchange reactions indicates that insulin B (ox) ions have two distinct structural types. In contrast, insulin B (red) ions have only one major reacting population, which has a more compact structure than the oxidized ions. No significant differences in fragmentation patterns for the two insulin B (ox) populations were observed when CID was performed as a function of deprotonating reaction time. However, markedly different fragmentation was found between [M + 4H]4+ of insulin B (ox) and (red). Therefore, the presence of cysteic acid groups in insulin B (ox) significantly impacts dissociation and presumably structure. This suggests that some insulin B (ox) ions are zwitterionic, with the five basic sites protonated and one cysteic acid group deprotonated. Molecular dynamics calculations revealed several viable structures that are consistent with the experimental results. For example, the most stable form of the reduced ion, which is unprotonated at the His10, is very compact and has lost the alpha-helix of native insulin. Low energy structures for the oxidized ions include a zwitterion with an intraionic interaction between anionic Cyx7 and cationic His10, as well as a nonzwitterionic conformer that lacks a proton at Phe1; both structures retain the alpha-helix. These structures may account for the two experimentally observed isomers, although others are possible. In addition, experiments on oxidized insulin B were conducted from methanolic solution, which may denature the conformation, and pure aqueous solution, which may leave a native conformation. These differences in solvent composition had no effect on the gas-phase results.     

5-Hexylidene-4-propylamino-1,5-dihydroimidazol-2-one formed from Cu-catalyzed oxidation with implication for the structure of a His-Lys cross-link

Cu-catalyzed oxidation of 5-hexyl-1,3-dihydroimidazo-2-one(1)in the presence of propylamine,as surrogates for the oxidized His side chain and Lys side chain,was investigated.5-Hexylidene-4-propylamino-1,5-dihydroimidazol-2-one(2),a model His-Lys cross-link product,was isolated and structurally characterized by NMR and mass spectrometry.     

Metal compound-mediated hydrolytic cleavage of oxidized insulin B chain:Regioselectivity and influence of peptide secondary structure

The interaction of oxidized insulin B chain(B)with cis-[Pd-(en)Cl2](en=ethylenediamine),cis-[Pd-(dtco-3-OH)Cl2](dtco-3-OH=dithiacyclooctan-3-ol)and CuCl2 was studied by electrospray inass spectrometry.It is discovered that the binding of Pd(Ⅱ)complexes and the sites of cleavage are highly dependent on the secondary structure and local environment of B.The hydrolytic cleavage of denatured B by Pd(Ⅱ)complexes was monitored by HPLC.The reaction is regioselective and follows first order kinetics with half-life of 4.8 days at 40℃.Two amide bonds,i.e.at Leu6-Cys7 and at Gly8-Ser9,which are close to the two potential Pd(Ⅱ)binding sites His5 and His10,are selectively cleaved.In the case of Cu(Ⅱ)ion as promoter,only one cleavage site was observed which is located at Gly8-Ser9 bond.These results provide improved understanding on the design of artificial metallopeptidase.     

Interaction of palladium(II) and platinum(II) complexes with microperoxidase-11 studied by electrospray mass spectrometry and MS/MS analysis

Interactions of cis-[Pd(en)(H(2)O)(2)](2+) (en, ethylenediamine) and cis-[Pt(NH(3))(2)(H(2)O)(2)](2+) with microperoxidase-11 (MP-11) in a molar ratio of 1:1 or 2:1 at pH 1.4 were investigated via electrospray mass spectrometry and MS/MS analysis at room temperature and at 40 degrees C with an incubation time of 2 or 3 days. The composition of the Pd(II)- and Pt(II)-anchored MP-11 was confirmed on the basis of the precise molecular mass and the simulated isotope distribution pattern. MS/MS analysis revealed that the Pd(II) center anchored to the side chain of Cys7 as Pd(II) and MP-11 were mixed in an equimolar ratio and to side chains of Cys7 and Cys4 as Pd(II) and MP-11 mixed in a 2:1 molar ratio. When Pt(II) and MP-11 were mixed in a 2:1 molar ratio, Pt(II) first anchored to the side chain of Cys7, and then to the side chain of Cys4 with time. The initial coordination of Pd(II) and Pt(II) to the side chain of Cys7 is the essential step for the Pd(II)- and Pt(II)-promoted cleavage of the His8-Thr9 bond in MP-11. These results support the hypothesis that the Pd(II)-mediated cleavage of the His18-Thr19 bond in cytochorome c is due to the identical binding mode.     

MOLECULAR CHANGES DURING THE PHOTOOXIDATION OF α-CRYSTALLIN IN THE PRESENCE OF UROPORPHYRIN

Singlet oxygen reacts preferentially with three amino acids in proteins, His, Trp and Met. In order to study the specific molecular events that result from such oxidations, calf a-crystallin was photooxidized in the presence of uroporphyrin and the reactions were investigated by high performance liquid chromatography peptide mapping using a photodiode array detector followed by fast atom bombardment mass spectrometry (FAB-MS). From these studies, the following conclusions can be inferred: (1) Upon photooxidation residue Met-68 of the B chain is oxidized to Met sulfoxide, whereas residue Trp-60 remains intact. (2) Two of the 16 His residues in a-crystallin are photooxidized with an apparent pK_a of ca 7.0. (3) FAB-MS analysis suggests that residue Lys-166 close to the C-terminal end of the A chain forms a cross-link with the His-7 residue close to the N-terminal end of the A chain. This may be either an inter- or intramolecular cross-link.