Literature DB >> 11841291

Phosphonate lipid tubules II.

Britt N Thomas1, Christopher M Lindemann, Robert C Corcoran, Casey L Cotant, Janet E Kirsch, Phillip J Persichini.   

Abstract

We describe a new chiral tubule-forming lipid in which the C-O-P phosphoryl linkage of the archetypal tubule-forming molecule, 1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine, "DC(8,9)PC", is replaced by a C-P linkage. Tubule formation with this phosphonate analogue proceeds under the same mild conditions as with DC(8,9)PC and produces similar yields, but synchrotron small-angle X-ray scattering, atomic force microscopy, and optical microscopy show the new tubules to have diameters 1.94 times as great, to be significantly shorter, and to be thinner-walled. A significant portion of the enantiomerically pure chiral phosphonate precipitate is in the form of stable open helices, and these helices are divided almost evenly between left- and right-handed members.

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Year:  2002        PMID: 11841291     DOI: 10.1021/ja012137a

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Chiral tubule self-assembly from an achiral diynoic lipid.

Authors:  Serhii Pakhomov; Robert P Hammer; Bijaya K Mishra; Britt N Thomas
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-07       Impact factor: 11.205

2.  Co-assembled nanotubes with controlled curvature radius using a hydrogen bond regulation strategy.

Authors:  Lai-Cheng Zhou; Yun-Han Yang; Ran He; Yang Qin; Ling Zhang
Journal:  RSC Adv       Date:  2021-10-22       Impact factor: 4.036

  2 in total

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