Polymerase activities and RNA structures in the atomic force microscope

被引:33
作者
Hansma, HG [1 ]
Golan, R
Hsieh, W
Daubendiek, SL
Kool, ET
机构
[1] Univ Calif Santa Barbara, Dept Phys, Santa Barbara, CA 93106 USA
[2] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
基金
美国国家科学基金会;
关键词
AFM; AMV reverse transcriptase; DNA rolling circle; enzyme assay; replication; ribozyme; Sequenase; scanning force microscope; SFM; scanning probe microscopy; SPM; Taq polymerase; transcription;
D O I
10.1006/jsbi.1999.4170
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The structures of the reaction products are the basis for novel polymerase assays using the atomic force microscope (AFM). Polymerases are the enzymes involved in transcription and replication of DNA Rapid semiquantitative estimates of the activity of DNA polymerases such as Sequenase, Tag polymerase, and AMV reverse transcriptase and RNA polymerases (RNAP) such as Escherichia coli RNAP were obtained from AFM images of the nucleic acids after polymerase reactions. DNA polymerases were assayed via replication of the single-stranded phi X-174 virion. RNAP was assayed via transcription, using a rolling circle DNA template that produces long strands of RNA. In some cases, AFM was better than agarose gel electrophoresis for assaying DNA polymerase activity, since aggregation prevented the DNA from entering the agarose gel. Extended molecules of single-stranded RNA synthesized with the rolling circle DNA template showed varied conformations and degrees of stretching. Some structural differences were observed between two RNAs-a ribozyme concatamer and an RNA with 90% purines. (C) 1999 Academic Press.
引用
收藏
页码:240 / 247
页数:8
相关论文
共 49 条
[1]   ATOMIC-FORCE MICROSCOPE MEASUREMENTS OF NUCLEOSOME CORES ASSEMBLED ALONG DEFINED DNA-SEQUENCES [J].
ALLEN, MJ ;
DONG, XF ;
ONEILL, TE ;
YAU, P ;
KOWALCZYKOWSKI, SC ;
GATEWOOD, J ;
BALHORN, R ;
BRADBURY, EM .
BIOCHEMISTRY, 1993, 32 (33) :8390-8396
[2]   Mapping individual cosmid DNAs by direct AFM imaging [J].
Allison, DP ;
Kerper, PS ;
Doktycz, MJ ;
Thundat, T ;
Modrich, P ;
Larimer, FW ;
Johnson, DK ;
Hoyt, PR ;
Mucenski, ML ;
Warmack, RJ .
GENOMICS, 1997, 41 (03) :379-384
[3]   Phase imaging of moving DNA molecules and DNA molecules replicated in the atomic force microscope [J].
Argaman, M ;
Golan, R ;
Thomson, NH ;
Hansma, HG .
NUCLEIC ACIDS RESEARCH, 1997, 25 (21) :4379-4384
[4]   MOTION AND ENZYMATIC DEGRADATION OF DNA IN THE ATOMIC-FORCE MICROSCOPE [J].
BEZANILLA, M ;
DRAKE, B ;
NUDLER, E ;
KASHLEV, M ;
HANSMA, PK ;
HANSMA, HG .
BIOPHYSICAL JOURNAL, 1994, 67 (06) :2454-2459
[5]   BIOCHEMICAL AND STRUCTURAL APPLICATIONS OF SCANNING FORCE MICROSCOPY [J].
BUSTAMANTE, C ;
ERIE, DA ;
KELLER, D .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1994, 4 (05) :750-760
[6]   Visualization and analysis of chromatin by scanning force microscopy [J].
Bustamante, C ;
Zuccheri, G ;
Leuba, SH ;
Yang, GL ;
Samori, B .
METHODS, 1997, 12 (01) :73-83
[7]   Scanning force microscopy under aqueous solutions [J].
Bustamante, C ;
Rivetti, C ;
Keller, DJ .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1997, 7 (05) :709-716
[8]   DNA looping by Ku and the DNA-dependent protein kinase [J].
Cary, RB ;
Peterson, SR ;
Wang, JT ;
Bear, DG ;
Bradbury, EM ;
Chen, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) :4267-4272
[9]  
Chamberlin M.J., 1982, ENZYMES, VXV, P61
[10]   ROLLING-CIRCLE RNA-SYNTHESIS - CIRCULAR OLIGONUCLEOTIDES AS EFFICIENT SUBSTRATES FOR T7 RNA-POLYMERASE [J].
DAUBENDIEK, SL ;
RYAN, K ;
KOOL, ET .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (29) :7818-7819