Feeling Inter- or Intramolecular Interactions with the Polymer Chain as Probe: Recent Progress in SMFS Studies on Macromolecular Interactions

被引:27
|
作者
Liu, Ningning [2 ]
Zhang, Wenke [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130012, Peoples R China
[2] Liaoning Shihua Univ, Sch Chem & Mat Sci, Fushun 113001, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
force spectroscopy; mechanochemistry; macromolecular interactions; scanning probe microscopy; single-molecule studies; MOLECULE FORCE SPECTROSCOPY; SINGLE-STRANDED-DNA; BACILLUS-SUBTILIS DNAD; INDIVIDUAL NUCLEOSOMES; THIOREDOXIN CATALYSIS; DYNAMIC STRENGTH; BINDING-PROTEIN; DISULFIDE BONDS; DOUBLE HELIX; ADHESION;
D O I
10.1002/cphc.201200154
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Single-molecule force spectroscopy (SMFS) opens new avenues for elucidating the structures and functions of large coiled molecules such as synthetic and biopolymers at the single-molecule level. In addition, some of the features in the forceextension curves (i.e. force spectra) are closely related to primary/secondary structures of the molecules being stretched. For example, the long force plateau in the DNA stretching curve is related to the double-helix structure. These features can be regarded as the force fingerprints of individual macromolecules. These force fingerprints can therefore be used as indicators/criteria of single-molecule manipulation during the measurement of some unknown intra- or intermolecular interactions. By comparing the force spectra of a single polymer chain before and after interaction with other molecules, the mode/strength of such molecular interactions can be derived. This Review focuses on recent advances in AFM-based SMFS studies on molecular interactions in both synthetic and biopolymer systems using a single macromolecular chain as probe, including interactions between nucleic acids and proteins, mechanochemistry of covalent bonds, conformation-regulated enzymatic reactions, adsorption and desorption of biopolymers on a flat surface or from the nanopore of a carbon nanotube, and polymer interactions in the condensed state.
引用
收藏
页码:2238 / 2256
页数:19
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