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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

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.

Abstract

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.

Introduction

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

Protocol

1. General materials and methods

  1. Refer to the Table of Materials file for the salts, chemicals, antibiotics, enzymes, antibodies, and resin materials used in this protocol.
  2. Prepare Luria-Bertani (LB) liquid medium, LB agar plates, HEPES buffer, SDS polyacrylamide gel electrophoresis (SDS-PAGE), Phosphate-buffered saline (PBS), Tris-EDTA (TE) buffer according to the recipes from cold spring harbor protocols45,46

Representative Results

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.......

Discussion

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.......

Acknowledgements

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.].

....

Materials

NameCompanyCatalog NumberComments
Anti-DigoxigeninRoche11214667001
BfaINew England Biolab (NEB)R0568S
BSASigma-AldrichV900933
CMOS camera MikrotronMC1362
CviAIINew England Biolab (NEB)R0640S
DIG-11-dUTPJena BioscienceNU-803-DIGXL
DNA extraction solutionG-CLONEEX0108
Dnase I, Rnase-Free, Hc EaThermo Fisher ScientificEN0523
dNTP mixtureNanjing Vazyme Biotech Co., Ltd (Vazyme)P032-02
DTTSolarbioD1070
Dynabeads M-270  beadsThermo Fisher Scientific65305Streptavidin beads
Dynabeads MyOne beadsThermo Fisher Scientific65001Streptavidin beads
EthanolTianjin No.6 Chemical Reagent Factory1083
GlycerolBeijing Hwrkchemical Co,. LtdSMG66258-1
ImidazoleSolarbioII0070
IPTGSolarbioI8070
IsopropanolTianjin No.6 Chemical Reagent FactoryA1079
KanamycinThermo Fisher ScientificEN0523
Klenow fragment (3′-5′ exo-)New England Biolab (NEB)M0212S
LabViewNational Instrumentshttps://www.ni.com/en-us/shop/product/labview.htmlGraphical programming software 
LiClBide Pharmatech Co., Ltd (bidepharm)BD136449
LysozymeSolarbioL8120-5
MseINew England Biolab (NEB)R0525S
NaClShanghai AladdinC111533
NanoDropThermo Fisher ScientificSpectrophotometer
NdeINew England Biolab (NEB)R0111S
Ni NTA Beads 6FFChangzhou Smart-Lifesciences Biotechnology Co.,LtdSA005025
Nitrocellulose membraneABclonalRM02801
PMSFSolarbioP8340
Proteinase KBeyotime Biotech Inc (beyotime)ST535-500mg
rCutSmart BufferNew England Biolab (NEB)B6004S
Rnase ASigma-AldrichR4875
Sodium acetateSERVA Electrophoresis GmbH2124902
Sumo proteaseBeyotime Biotech Inc (beyotime)P2312M

References

  1. Blackburn, E. H., Epel, E. S., Lin, J. Human telomere biology: A contributory and interactive factor in aging, disease risks, and protection. Science. 350 (6265), 1193-1198 (2015).
  2. Li, N., et al.

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