Evidence map›Paper›PMID 28549727›Full record

ArticleBiochimica et biophysica acta. Biomembranes2017

Topographic analysis by atomic force microscopy of proteoliposomes matrix vesicle mimetics harboring TNAP and AnxA5.

Maytê Bolean, Ivana A Borin, Ana M S Simão, Massimo Bottini, Luis A Bagatolli, Marc F Hoylaerts, José L Millán, Pietro Ciancaglini

Abstract read
In one paragraph

Article in Biochimica et biophysica acta. Biomembranes, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Maytê BoleanDepto. Química, FFCLRP-USP, Universidade de São Paulo, Ribeirão Preto, SP, Brazil. Electronic address: maytebolean@usp.br.
Ivana A BorinDepto. Química, FFCLRP-USP, Universidade de São Paulo, Ribeirão Preto, SP, Brazil.
Ana M S SimãoDepto. Química, FFCLRP-USP, Universidade de São Paulo, Ribeirão Preto, SP, Brazil.
Massimo BottiniDepartment of Experimental Medicine and Surgery, University of Rome Tor Vergata, Rome, Italy; Inflammatory and Infectious Disease Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Luis A BagatolliMEMPHYS - Center for Biomembrane Physics, University of Southern Denmark, Odense, Denmark.
Marc F HoylaertsDepartment of Cardiovascular Sciences, Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.
José L MillánSanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Pietro CiancagliniDepto. Química, FFCLRP-USP, Universidade de São Paulo, Ribeirão Preto, SP, Brazil. Electronic address: pietro@ffclrp.usp.br.

Funding

MOLECULAR PATHOGENESIS/TREATMENT OF HYPOPHOSPHATASIAR01DE012889 · NIDCR · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI MILLAN, JOSE LUIS · 1999 to 2020
$9.2M
Mechanisms of initiation of skeletal mineralizationR01AR053102 · NIAMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI MILLAN, JOSE LUIS · 2006 to 2015
$3.8M
NIAMS NIH HHS R01 AR053102NIDCR NIH HHS R01 DE012889NIH HHS AR53102NIH HHS DE12889
6 · The paper itself

Abstract

Atomic force microscopy (AFM) is one of the most commonly used scanning probe microscopy techniques for nanoscale imaging and characterization of lipid-based particles. However, obtaining images of such particles using AFM is still a challenge. The present study extends the capabilities of AFM to the characterization of proteoliposomes, a special class of liposomes composed of lipids and proteins, mimicking matrix vesicles (MVs) involved in the biomineralization process. To this end, proteoliposomes were synthesized, composed of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and 1,2-dipalmitoyl-sn-glycero-3-phospho-l-serine (DPPS), with inserted tissue-nonspecific alkaline phosphatase (TNAP) and/or annexin V (AnxA5), both characteristic proteins of osteoblast-derived MVs. We then aimed to study how TNAP and AnxA5 insertion affects the proteoliposomes' membrane properties and, in turn, interactions with type II collagen, thus mimicking early MV activity during biomineralization. AFM images of these proteoliposomes, acquired in dynamic mode, revealed the presence of surface protrusions with distinct viscoelasticity, thus suggesting that the presence of the proteins induced local changes in membrane fluidity. Surface protrusions were measurable in TNAP-proteoliposomes but barely detectable in AnxA5-proteoliposomes. More complex surface structures were observed for proteoliposomes harboring both TNAP and AnxA5 concomitantly, resulting in a lower affinity for type II collagen fibers compared to proteoliposomes harboring AnxA5 alone. The present study achieved the topographic analysis of lipid vesicles by direct visualization of structural changes, resulting from protein incorporation, without the need for fluorescent probes.

Indexed as

1,2-DipalmitoylphosphatidylcholineAlkaline PhosphataseAnimalsAnnexin A5BiomimeticsCalcification, PhysiologicCarrier ProteinsCollagen Type IILiposomesMembrane FluidityMembrane LipidsMicroscopy, Atomic ForceProteolipidsRatsSerine1,2-DipalmitoylphosphatidylcholineAlkaline PhosphataseAnnexin A5Carrier Proteinscolfosceril palmitateCollagen Type IILiposomesMembrane LipidsProteolipidsproteoliposomesSerineAnnexin VAtomic force microscopyCollagenMatrix vesiclesProteoliposomesTissue-nonspecific alkaline phosphatase

Identifiers

PMID28549727
PMCPMC5793902

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.