Literature DB >> 8873062

Collagen fibril surface: TMAFM, FEG-SEM and freeze-etching observations.

M Raspanti1, A Alessandrini, P Gobbi, A Ruggeri.   

Abstract

Native, unfixed collagen fibrils from rat tail tendon were dehydrated following different procedures and observed under a FEG-SEM and an AFM operated in Tapping Mode (TMAFM). Freeze-etched, untreated fibrils from the same tissue were also observed for comparison. The most notable features of the fibril surface, i.e., the gap/overlap alternation and three prominent intraperiod ridges, were simultaneously visible only in freeze-etched specimens, while under the SEM and the TMAFM their appearance was dependent on both the dehydration procedure and the visualization technique. The different susceptibility of the collagen fibril surface structures to various treatments clearly implies the existence of domains of different composition. Moreover, identical specimens were imaged differently by SEM and TMAFM, highlighting instrument-specific advantages and limitations. The onset of dehydration-dependent, procedure-specific artifacts should be considered in high-resolution studies of connective tissues. As for any biological specimen, the final aspect of collagen fibrils is determined no less by the preliminary treatments than by the visualization approach.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8873062     DOI: 10.1002/(SICI)1097-0029(19960901)35:1<87::AID-JEMT8>3.0.CO;2-P

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  8 in total

1.  The nanometre-scale physiology of bone: steric modelling and scanning transmission electron microscopy of collagen-mineral structure.

Authors:  Benjamin Alexander; Tyrone L Daulton; Guy M Genin; Justin Lipner; Jill D Pasteris; Brigitte Wopenka; Stavros Thomopoulos
Journal:  J R Soc Interface       Date:  2012-02-16       Impact factor: 4.118

2.  Collagen fibril architecture, domain organization, and triple-helical conformation govern its proteolysis.

Authors:  Shiamalee Perumal; Olga Antipova; Joseph P R O Orgel
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-14       Impact factor: 11.205

3.  Observation of collagen fibrils produced by osteosarcoma cells using atomic force microscopy.

Authors:  Osamu Hoshi
Journal:  Med Mol Morphol       Date:  2013-11-07       Impact factor: 2.309

4.  Collagen fibril surface displays a constellation of sites capable of promoting fibril assembly, stability, and hemostasis.

Authors:  J P R O Orgel; O Antipova; I Sagi; A Bitler; D Qiu; R Wang; Y Xu; J D San Antonio
Journal:  Connect Tissue Res       Date:  2010-11-30       Impact factor: 3.417

5.  Tissue section AFM: In situ ultrastructural imaging of native biomolecules.

Authors:  Helen K Graham; Nigel W Hodson; Judith A Hoyland; Sarah J Millward-Sadler; David Garrod; Anthea Scothern; Christopher E M Griffiths; Rachel E B Watson; Thomas R Cox; Janine T Erler; Andrew W Trafford; Michael J Sherratt
Journal:  Matrix Biol       Date:  2010-02-06       Impact factor: 11.583

6.  Cryptic binding sites become accessible through surface reconstruction of the type I collagen fibril.

Authors:  Jie Zhu; Cody L Hoop; David A Case; Jean Baum
Journal:  Sci Rep       Date:  2018-11-09       Impact factor: 4.379

Review 7.  Marine origin collagens and its potential applications.

Authors:  Tiago H Silva; Joana Moreira-Silva; Ana L P Marques; Alberta Domingues; Yves Bayon; Rui L Reis
Journal:  Mar Drugs       Date:  2014-12-05       Impact factor: 5.118

Review 8.  Revealing Accessibility of Cryptic Protein Binding Sites within the Functional Collagen Fibril.

Authors:  Cody L Hoop; Jie Zhu; Ana Monica Nunes; David A Case; Jean Baum
Journal:  Biomolecules       Date:  2017-11-01
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.