Biofunctionalization of a generic collagenous triple helix with the α2β1 integrin binding site allows molecular force measurements

International Journal of Biochemistry and Cell Biology

Volumn 43, Issue 5, 2011, Pages 721-731

  Niland, Stephan ^a   Westerhausen, Christoph ^b   Schneider, Stefan W ^c   Eckes, Beate ^d   Schneider, Matthias F ^e   Eble, Johannes A ^a  

^a UNIVERSITY HOSPITAL FRANKFURT   (Germany)

^b UNIVERSITY OF AUGSBURG   (Germany)

^c UNIVERSITY OF HEIDELBERG   (Germany)

^d UNIVERSITY OF COLOGNE   (Germany)

^e BOSTON UNIVERSITY   (United States)

Author keywords

2 1 integrin; Atomic force microscopy; Biofunctionalization; Cell adhesion; Mini collagen; Triple helicity

Indexed keywords

COLLAGEN TYPE 1; VERY LATE ACTIVATION ANTIGEN 2;

ARTICLE; ATOMIC FORCE MICROSCOPY; BINDING SITE; COVALENT BOND; CROSS LINKING; FETUS; FIBROBLAST; FOCAL ADHESION; FORCE; HUMAN; HUMAN CELL; HYDROXYLATION; PLASMID; PROTEIN BINDING; TENSILE STRENGTH; TRIPLE HELIX;

ANIMALS; BINDING SITES; BIOMECHANICS; CATTLE; CELL LINE, TUMOR; COLLAGEN TYPE I; EXTRACELLULAR MATRIX; HUMANS; INTEGRIN ALPHA2BETA1; MICROSCOPY, ATOMIC FORCE; PROTEIN STRUCTURE, SECONDARY; RECOMBINANT PROTEINS; REPETITIVE SEQUENCES, AMINO ACID;

EID: 79953183313     PISSN: 13572725     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biocel.2011.01.013     Document Type: Article

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