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This protocol demonstrates using single-molecule magnetic tweezers to study interactions between telomeric DNA-binding proteins (Telomere Repeat-binding Factor 1 [TRF1] and TRF2) and long telomeres extracted from human cells. It describes the preparatory steps for telomeres and telomeric repeat-binding factors, the execution of single-molecule experiments, and the data collection and analysis methods.
Telomeres, the protective structures at the ends of chromosomes, are crucial for maintaining cellular longevity and genome stability. Their proper function depends on tightly regulated processes of replication, elongation, and damage response. The shelterin complex, especially Telomere Repeat-binding Factor 1 (TRF1) and TRF2, plays a pivotal role in telomere protection and has emerged as a potential anti-cancer target for drug discovery. These proteins bind to the repetitive telomeric DNA motif TTAGGG, facilitating the formation of protective structures and recruitment of other telomeric proteins. Structural methods and advanced imaging techniques have provided insights into telomeric protein-DNA interactions, but probing the dynamic processes requires single-molecule approaches. Tools like magnetic tweezers, optical tweezers, and atomic force microscopy (AFM) have been employed to study telomeric protein-DNA interactions, revealing important details such as TRF2-dependent DNA distortion and telomerase catalysis. However, the preparation of single-molecule constructs with telomeric repetitive motifs continues to be a challenging task, potentially limiting the breadth of studies utilizing single-molecule mechanical methods. To address this, we developed a method to study interactions using full-length human telomeric DNA with magnetic tweezers. This protocol describes how to express and purify TRF2, prepare telomeric DNA, set up single-molecule mechanical assays, and analyze data. This detailed guide will benefit researchers in telomere biology and telomere-targeted drug discovery.
Telomeres are protective structures at the ends of chromosomes1,2,3. Telomere erosion during cell division leads to cell senescence and aging, while abnormal elongation of telomeres contributes to cancer4,5. For telomeres to function properly, their replication, elongation, and damage responses must be highly regulated6,7,8. Shelterin, composed of six subunits, plays a central role in telomere protection9
1. General materials and methods
Figure 1A illustrates the schematic domains and structures of TRF1 and TRF2, consisting of 439 and 542 amino acids, respectively, which can be expressed in prokaryotic cells. The preparation of TRF1 has been previously described in the literature41. Here, we provide a comprehensive description and representative results of the preparation of TRF2. Figure 1B shows the plasmid map used for expressing TRF2 in E. coli. We evaluated T.......
This protocol employs magnetic tweezers for the manipulation of TRFs at the single-molecule level57,58,59. We utilize magnetic beads to separate TRFs from genomic DNA fragments. Following restriction digestion, TRFs bind to the magnetic beads, enabling their easy separation from genomic DNA fragments. This approach allows for manipulation using magnetic tweezers, which can effectively trap magnetic beads, unlike optical tweezers.......
This work was supported by the National Natural Science Foundation of China [Grant 32071227 to Z.Y.], Tianjin Municipal Natural Science Foundation of China (22JCYBJC01070 to Z.Y.), and State Key Laboratory of Precision Measuring Technology and Instruments (Tianjin University) [Grant pilab2210 to Z.Y.].
....Name | Company | Catalog Number | Comments |
Anti-Digoxigenin | Roche | 11214667001 | |
BfaI | New England Biolab (NEB) | R0568S | |
BSA | Sigma-Aldrich | V900933 | |
CMOS camera | Mikrotron | MC1362 | |
CviAII | New England Biolab (NEB) | R0640S | |
DIG-11-dUTP | Jena Bioscience | NU-803-DIGXL | |
DNA extraction solution | G-CLONE | EX0108 | |
Dnase I, Rnase-Free, Hc Ea | Thermo Fisher Scientific | EN0523 | |
dNTP mixture | Nanjing Vazyme Biotech Co., Ltd (Vazyme) | P032-02 | |
DTT | Solarbio | D1070 | |
Dynabeads M-270 beads | Thermo Fisher Scientific | 65305 | Streptavidin beads |
Dynabeads MyOne beads | Thermo Fisher Scientific | 65001 | Streptavidin beads |
Ethanol | Tianjin No.6 Chemical Reagent Factory | 1083 | |
Glycerol | Beijing Hwrkchemical Co,. Ltd | SMG66258-1 | |
Imidazole | Solarbio | II0070 | |
IPTG | Solarbio | I8070 | |
Isopropanol | Tianjin No.6 Chemical Reagent Factory | A1079 | |
Kanamycin | Thermo Fisher Scientific | EN0523 | |
Klenow fragment (3′-5′ exo-) | New England Biolab (NEB) | M0212S | |
LabView | National Instruments | https://www.ni.com/en-us/shop/product/labview.html | Graphical programming software |
LiCl | Bide Pharmatech Co., Ltd (bidepharm) | BD136449 | |
Lysozyme | Solarbio | L8120-5 | |
MseI | New England Biolab (NEB) | R0525S | |
NaCl | Shanghai Aladdin | C111533 | |
NanoDrop | Thermo Fisher Scientific | Spectrophotometer | |
NdeI | New England Biolab (NEB) | R0111S | |
Ni NTA Beads 6FF | Changzhou Smart-Lifesciences Biotechnology Co.,Ltd | SA005025 | |
Nitrocellulose membrane | ABclonal | RM02801 | |
PMSF | Solarbio | P8340 | |
Proteinase K | Beyotime Biotech Inc (beyotime) | ST535-500mg | |
rCutSmart Buffer | New England Biolab (NEB) | B6004S | |
Rnase A | Sigma-Aldrich | R4875 | |
Sodium acetate | SERVA Electrophoresis GmbH | 2124902 | |
Sumo protease | Beyotime Biotech Inc (beyotime) | P2312M |
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