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1
Reconstitution of rods from tobacco mosaic virus protein and RNA modified with bulky carcinogens.由烟草花叶病毒蛋白和经大分子致癌物修饰的RNA重构视杆细胞。
Proc Natl Acad Sci U S A. 1982 Apr;79(8):2541-3. doi: 10.1073/pnas.79.8.2541.
2
Infectivity and reconstitution of TMV RNA modified with N-acetoxy-2-acetylaminofluorene or benzol [a] pyrene 7,8-dihydrodiol 9,10 oxide.用N-乙酰氧基-2-乙酰氨基芴或苯并[a]芘7,8-二氢二醇9,10-环氧化物修饰的烟草花叶病毒RNA的感染性和重组。
Nucleic Acids Res. 1980 May 10;8(9):2067-74. doi: 10.1093/nar/8.9.2067.
3
Studies on the mechanism of assembly of tobacco mosaic virus.烟草花叶病毒装配机制的研究。
Biophys J. 1980 Oct;32(1):313-29. doi: 10.1016/S0006-3495(80)84959-9.
4
Modulation of DNA adduct formation by successive exposures of DNA to small and bulky chemical carcinogens.通过使DNA连续暴露于小分子和大分子化学致癌物来调节DNA加合物的形成。
Carcinogenesis. 1995 Dec;16(12):3057-62. doi: 10.1093/carcin/16.12.3057.
5
Mechanism of benzo[a]pyrene diol epoxide induced deoxyribonucleic acid strand scission.苯并[a]芘二醇环氧化物诱导脱氧核糖核酸链断裂的机制。
Biochemistry. 1980 Aug 19;19(17):3948-56. doi: 10.1021/bi00558a009.
6
High mobility group 1 and 2 proteins bind preferentially to DNA that contains bulky adducts induced by benzo[a]pyrene diol epoxide and N-acetoxy-acetylaminofluorene.高迁移率族蛋白1和2优先结合含有苯并[a]芘二氢二醇环氧化物和N-乙酰氧基-乙酰氨基芴诱导的大分子加合物的DNA。
Cancer Lett. 2000 Sep 29;158(1):17-25. doi: 10.1016/s0304-3835(00)00517-6.
7
Coordinated two-disk nucleation, growth and properties, of virus-like particles assembled from tobacco-mosaic-virus capsid protein with poly(A) or oligo(A) of different length.由烟草花叶病毒衣壳蛋白与不同长度的聚(A)或寡聚(A)组装而成的病毒样颗粒的双盘协同成核、生长及性质
Eur J Biochem. 1984 Apr 2;140(1):119-27. doi: 10.1111/j.1432-1033.1984.tb08074.x.
8
Assembly of rod-shaped virus in vitro: reconstitution with cucumber green mottle mosaic virus protein and tobacco mosaic virus RNA.体外杆状病毒的组装:用黄瓜绿斑驳花叶病毒蛋白和烟草花叶病毒RNA进行重组
Proc Natl Acad Sci U S A. 1972 Dec;69(12):3680-3. doi: 10.1073/pnas.69.12.3680.
9
Translation of satellite tobacco necrosis virus RNA modified by (not equal to)-r-7,t-8-dihydroxy-t-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene is inhibited in a wheat germ cell-free system.在小麦胚无细胞系统中,由(不相等)-r-7,t-8-二羟基-t-9,10-环氧-7,8,9,10-四氢苯并[a]芘修饰的卫星烟草坏死病毒RNA的翻译受到抑制。
Carcinogenesis. 1983;4(2):221-5. doi: 10.1093/carcin/4.2.221.
10
Assembly of tobacco mosaic virus in vitro. Improved model for the elongation process by protein subunits.烟草花叶病毒的体外组装。蛋白质亚基延伸过程的改进模型。
J Biochem. 1975 Jun;77(6):1157-63.

本文引用的文献

1
Reconstitution of tobacco mosaic virus. III. Improved methods and the use of mixed nucleic acids.烟草花叶病毒的重组。III. 改进方法及混合核酸的应用。
Biochim Biophys Acta. 1959 Jun;33(2):359-70. doi: 10.1016/0006-3002(59)90126-x.
2
Degradation of tobacco mosaic virus with acetic acid.用乙酸降解烟草花叶病毒。
Virology. 1957 Aug;4(1):1-4. doi: 10.1016/0042-6822(57)90038-7.
3
Separation of large denatured peptides by reverse phase high performance liquid chromatography. Trifluoroacetic acid as a peptide solvent.通过反相高效液相色谱法分离大的变性肽。三氟乙酸作为肽溶剂。
J Biol Chem. 1980 Dec 10;255(23):11199-203.
4
The structural domains of cAMP-dependent protein kinase I. Characterization of two sites of proteolytic cleavage and homologies to cAMP-dependent protein kinase II.环磷酸腺苷(cAMP)依赖性蛋白激酶I的结构域。蛋白水解切割两个位点的特性及与环磷酸腺苷依赖性蛋白激酶II的同源性。
J Biol Chem. 1980 Oct 25;255(20):9706-12.
5
Identification of two subclasses of type II cAMP-dependent protein kinases. Neural-specific and non-neural protein kinases.II型环磷酸腺苷依赖性蛋白激酶两个亚类的鉴定。神经特异性和非神经蛋白激酶。
J Biol Chem. 1980 Sep 10;255(17):8179-84.
6
Morphology of bovine fibrinogen monomers and fibrin oligomers.牛纤维蛋白原单体和纤维蛋白寡聚体的形态学
J Mol Biol. 1981 Aug 15;150(3):399-408. doi: 10.1016/0022-2836(81)90555-6.
7
The structures and related functions of phosphorylase a.磷酸化酶a的结构及相关功能。
Annu Rev Biochem. 1980;49:31-61. doi: 10.1146/annurev.bi.49.070180.000335.
8
Structure, specificity and localization of the serine proteases of connective tissue.结缔组织丝氨酸蛋白酶的结构、特异性及定位
FEBS Lett. 1980 Jun 2;114(2):189-96. doi: 10.1016/0014-5793(80)81112-4.
9
Infectivity and reconstitution of TMV RNA modified with N-acetoxy-2-acetylaminofluorene or benzol [a] pyrene 7,8-dihydrodiol 9,10 oxide.用N-乙酰氧基-2-乙酰氨基芴或苯并[a]芘7,8-二氢二醇9,10-环氧化物修饰的烟草花叶病毒RNA的感染性和重组。
Nucleic Acids Res. 1980 May 10;8(9):2067-74. doi: 10.1093/nar/8.9.2067.
10
Studies on the site in the regulatory subunit of type I cAMP-dependent protein kinase phosphorylated by cGMP-dependent protein kinase.关于被环鸟苷酸依赖性蛋白激酶磷酸化的I型环磷酸腺苷依赖性蛋白激酶调节亚基上位点的研究。
J Biol Chem. 1981 Jun 10;256(11):5604-7.

由烟草花叶病毒蛋白和经大分子致癌物修饰的RNA重构视杆细胞。

Reconstitution of rods from tobacco mosaic virus protein and RNA modified with bulky carcinogens.

作者信息

Fraenkel-Conrat H, Singer B, Takanami Y, Santella R M, Grunberger D

出版信息

Proc Natl Acad Sci U S A. 1982 Apr;79(8):2541-3. doi: 10.1073/pnas.79.8.2541.

DOI:10.1073/pnas.79.8.2541
PMID:6806813
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC346235/
Abstract

Tobacco mosaic virus (TMV) RNA was treated with radioactive N-acetoxy-2-acetylaminofluorene (N-acetoxy-AAF) and (+/-)-7 beta, 8 alpha-dihydroxy-9 alpha, 10 alpha-epoxy-7,8,9,10-tetrahydrobenzo(a)pyrene (BaP diol epoxide) to obtain 3-25 adducts per molecule. Modified full length 30S RNAs and unmodified RNA were reconstituted for various time periods with TMV protein. The particulate products were separated by ultracentrifugation, and the amounts of virus-like material were quantitated by UV spectrophotometry. The length distribution and general appearance of the virus-like rods were studied by electron microscopy. Neither type of carcinogen prevented typical rod formation, but the rate of formation and the maximal yield of reconstituted particles diminished with increasing modification by both agents. The rod length distribution also showed progressively lesser numbers of full-length virus rods. The particulate material contained approximately the same number of adducts as the modified RNA. Thus, it appears that these carcinogen modifications of guanine residues at the N-2 or C-8 atoms did not prevent orderly protein assembly on the RNA but instead slowed up this process and frequently stopped it, possibly at sites where adducts happen to be clustered.

摘要

烟草花叶病毒(TMV)RNA用放射性N-乙酰氧基-2-乙酰氨基芴(N-乙酰氧基-AAF)和(±)-7β,8α-二羟基-9α,10α-环氧-7,8,9,10-四氢苯并[a]芘(BaP二醇环氧化物)处理,以获得每个分子3至25个加合物。将修饰的全长30S RNA和未修饰的RNA与TMV蛋白在不同时间段进行重组。通过超速离心分离颗粒产物,并通过紫外分光光度法定量病毒样物质的量。通过电子显微镜研究病毒样杆的长度分布和总体外观。两种致癌物均未阻止典型杆状结构的形成,但随着两种试剂修饰程度的增加,重组颗粒的形成速率和最大产量均降低。杆长度分布也显示全长病毒杆的数量逐渐减少。颗粒物质中加合物的数量与修饰的RNA大致相同。因此,看来这些在鸟嘌呤残基的N-2或C-8原子处的致癌物修饰并未阻止蛋白质在RNA上有序组装,而是减慢了这一过程并经常使其停止,可能是在加合物碰巧聚集的位点。