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      Proteogenomic Characterization of the Cement and Adhesive Gland of the Pelagic Gooseneck Barnacle Lepas anatifera

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          Abstract

          We focus on the stalked goose barnacle L. anatifera adhesive system, an opportunistic less selective species for the substrate, found attached to a variety of floating objects at seas. Adhesion is an adaptative character in barnacles, ensuring adequate positioning in the habitat for feeding and reproduction. The protein composition of the cement multicomplex and adhesive gland was quantitatively studied using shotgun proteomic analysis. Overall, 11,795 peptide sequences were identified in the gland and 2206 in the cement, clustered in 1689 and 217 proteinGroups, respectively. Cement specific adhesive proteins (CPs), proteases, protease inhibitors, cuticular and structural proteins, chemical cues, and many unannotated proteins were found, among others. In the cement, CPs were the most abundant (80.5%), being the bulk proteins CP100k and -52k the most expressed of all, and CP43k-like the most expressed interfacial protein. Unannotated proteins comprised 4.7% of the cement proteome, ranking several of them among the most highly expressed. Eight of these proteins showed similar physicochemical properties and amino acid composition to known CPs and classified through Principal Components Analysis (PCA) as new CPs. The importance of PCA on the identification of unannotated non-conserved adhesive proteins, whose selective pressure is on their relative amino acid abundance, was demonstrated.

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          Most cited references49

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          A simple method for displaying the hydropathic character of a protein.

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            Thermostability and aliphatic index of globular proteins.

            A Ikai (1980)
            A statistical analysis shows that the aliphatic index, which is defined as the relative volume of a protein occupied by aliphatic side chains (alanine, valine, isoleucine, and leucine), of proteins of thermophilic bacteria is significantly higher than that of ordinary proteins. The index may be regarded as a positive factor for the increase of thermostability of globular proteins.
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              Ultrasensitive proteome analysis using paramagnetic bead technology

              In order to obtain a systems-level understanding of a complex biological system, detailed proteome information is essential. Despite great progress in proteomics technologies, thorough interrogation of the proteome from quantity-limited biological samples is hampered by inefficiencies during processing. To address these challenges, here we introduce a novel protocol using paramagnetic beads, termed Single-Pot Solid-Phase-enhanced Sample Preparation (SP3). SP3 provides a rapid and unbiased means of proteomic sample preparation in a single tube that facilitates ultrasensitive analysis by outperforming existing protocols in terms of efficiency, scalability, speed, throughput, and flexibility. To illustrate these benefits, characterization of 1,000 HeLa cells and single Drosophila embryos is used to establish that SP3 provides an enhanced platform for profiling proteomes derived from sub-microgram amounts of material. These data present a first view of developmental stage-specific proteome dynamics in Drosophila at a single-embryo resolution, permitting characterization of inter-individual expression variation. Together, the findings of this work position SP3 as a superior protocol that facilitates exciting new directions in multiple areas of proteomics ranging from developmental biology to clinical applications.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                25 March 2021
                April 2021
                : 22
                : 7
                : 3370
                Affiliations
                [1 ]CIIMAR—Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Rua General Norton de Matos s/n, Terminal de Cruzeiros do Porto de Leixões, 4450-208 Matosinhos, Portugal; dany.perez@ 123456ciimar.up.pt (D.D.-P.); danielaalmeida23@ 123456gmail.com (D.A.); andre.machado@ 123456ciimar.up.pt (A.M.M.); aantunes@ 123456ciimar.up.pt (A.A.); filipe.castro@ 123456ciimar.up.pt (L.F.C.); vmvascon@ 123456fc.up.pt (V.V.); amoclclix@ 123456gmail.com (A.C.)
                [2 ]Cellular Proteomics Research, Helmholtz Centre for Infection Research, Inhoffenstraße. 7, 38124 Braunschweig, Germany; Josef.Wissing@ 123456helmholtz-hzi.de (J.W.); Lothar.Jaensch@ 123456Helmholtz-HZI.de (L.J.)
                [3 ]Biology Department, Faculty of Sciences, University of Porto, Rua do Campo Alegre, s/n, 4169-007 Porto, Portugal
                Author notes
                [* ]Correspondence: isabel.cunha@ 123456ciimar.up.pt ; Tel.: +351-22-340-1800; Fax: +351-22-339-0608
                Author information
                https://orcid.org/0000-0002-5211-972X
                https://orcid.org/0000-0002-9874-933X
                https://orcid.org/0000-0002-0320-5883
                https://orcid.org/0000-0002-6857-7581
                https://orcid.org/0000-0002-1328-1732
                https://orcid.org/0000-0003-3585-2417
                https://orcid.org/0000-0002-6149-9840
                Article
                ijms-22-03370
                10.3390/ijms22073370
                8037658
                33806079
                e6a50f4b-0d76-4fbb-9787-46b8a1802322
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 23 February 2021
                : 22 March 2021
                Categories
                Article

                Molecular biology
                underwater adhesion,cement protein,shotgun proteomics,ibaq,protein expression,mass spectrometry

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