The cytotoxic Staphylococcus aureus PSMα3 reveals a cross-α amyloid-like fibril

Author:

Tayeb-Fligelman Einav1ORCID,Tabachnikov Orly1ORCID,Moshe Asher1,Goldshmidt-Tran Orit1ORCID,Sawaya Michael R.2ORCID,Coquelle Nicolas3,Colletier Jacques-Philippe3,Landau Meytal1ORCID

Affiliation:

1. Department of Biology, Technion-Israel Institute of Technology, Haifa 3200003, Israel.

2. Department of Biological Chemistry, Department of Chemistry and Biochemistry, and Howard Hughes Medical Institute, University of California at Los Angeles, Los Angeles, CA 90095, USA.

3. Institut de Biologie Structurale (IBS), Université Grenoble Alpes–CEA–CNRS UMR 5075, Grenoble 38044, France.

Abstract

What's in a fold? Bacterially secreted peptides known as PSMs (phenol-soluble modulins) stimulate inflammatory responses, lyse human cells, and contribute to biofilm structuring. PSMα3 is a virulent 22-residue amyloid peptide secreted by Staphylococcus aureus. Tayeb-Fligelman et al. present a high-resolution structure encompassing the full length of the amyloid's sequence. This structure reveals an unexpected departure from the common amyloid cross-β folded architecture. Instead, PSMα3 forms amphipathic α-helices that are folded to stack perpendicular to the fibril axis into sheets. This unusual cross-α structure was important for fibril toxicity. Science , this issue p. 831

Funder

Agence Nationale de la Recherche

Association France Alzheimer

U.S.-Israel Binational Science Foundation

The I-CORE Program of the Planning and Budgeting Committee and The Israel Science Foundation

The Support for training and career development of researchers (Marie Curie) CIG, Seventh Framework Program (FP7) of the European Commission, Single Beneficiary

BioStruct-X

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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