Abstract

Single-molecule force spectroscopy with an atomic force microscope has been widely used to study inter- and intramolecular interactions. To obtain data consistent with single molecular events, a well-defined method is critical to limit the number of molecules at the apex of an AFM probe to one or to a few. In this paper, we demonstrate an easy method for single-molecule probe modification by using the Cu-catalyzed alkyne–azide cycloaddition reaction. Excess terminal alkynes were covalently attached to the probe, and a bi-functional molecule containing an azide at one end and a carboxylic acid at the other was dissolved in the reaction solution. By simply contacting the probe and the Cu substrate, controlled carboxylation on the probe apex could be achieved, since the ‘click’ reaction requires the co-exist of alkyne, azide and Cu(I). The finite contact area would result in a highly defined surface functionality of the probe down to single molecule level with high reproducibility.

Highlights

  • Single-molecule force spectroscopy (SMFS) has become one of the most powerful tools for studying inter- and intramolecular interactions [1]

  • (1) The forces appeared at a tip–surface separation of around 25 nm, which is the contour length of the poly(ethylene glycol) (PEG) we used

  • It was reasonable to believe that carboxylic groups from the azide molecules had been ‘clicked’ onto the atomic force microscopy (AFM) probes through our method

Read more

Summary

Introduction

Single-molecule force spectroscopy (SMFS) has become one of the most powerful tools for studying inter- and intramolecular interactions [1]. We report a new method for the modification of a single-molecule probe with highly defined surface functionality by using copper-catalyzed alkyne–azide cycloaddition (Figure 1). The probe was mounted onto an AFM, and brought into contact with a copper-filmcoated substrate for 5 to 10 s in a solution containing bi-functional molecules with a carboxylic acid group at one end and an azide group at the other end.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call