Structural and functional swapping of amyloidogenic and antimicrobial peptides: Redefining the role of amyloidogenic propensity in disease and host defense

被引:4
作者
Yadav, Jay Kant [1 ]
机构
[1] Cent Univ Rajasthan, Dept Biotechnol, NH-8 Bandersindri, Ajmer 305817, Rajasthan, India
关键词
amyloid; amyloidogenic peptides; antimicrobial activities; antimicrobial peptides; functional swapping; MEMBRANE INTERACTION; AGGREGATION; PROTEIN; INFECTION; FIBRILS; BINDING;
D O I
10.1002/psc.3378
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Peptides constitute an essential component of all organisms' protein homeostasis ranging from bacteria, plants, and animals. They have organically been evolved to perform a wide range of essential functions, including their role as neurotransmitters, antimicrobial peptides (AMPs), and hormones. AMPs are short peptides synthesized by almost all organisms, implicated in guarding the host from various microbial infections. Their inherent ability to differentiate the target microbes from the host confers them excellent prospects in fighting against microbial infections and affirming their robust therapeutic potential against numerous drug-resistant microbes. Amyloidogenic peptides (AMYs) represent another class of short peptides armed with inherent aggregation propensity and form fibrillar aggregates rich in cross beta-sheet structure. They are often involved in various degenerative diseases, including Alzheimer's disease (AD), Parkinson's disease (PD), and type-2 diabetes. Although these two distinct classes of peptides (i.e., AMPs and AMYs) appear to be functionally divergent, recent studies suggest that they possess a significant degree of structural and functional reciprocity. Consistent with this, many AMPs display amphiphilic nature, and hence, they can facilitate membrane remodeling processes, such as pore formation and fusion, similar to AMYs. The mounting evidence suggests the inherent ability of AMPs to self-assemble to form amyloid-like structures. On the other hand, the demonstration of antimicrobial properties of AMYs in their monomeric conformation provides a hint about the existence of an evolutionary linkage between these two classes of peptides. The congregation of specific amino acids to form aggregation-prone regions in a protein/peptide might have served as an evolutionary reservoir from which AMPs and AMYs were consecutively evolved. The current article reviews the fundamental features of the AMPs, AMYs, and their inter-relatedness and emerging paradigm for their inter-conversion.
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页数:9
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共 62 条
  • [1] Gastrointestinal Immunity and Alpha-Synuclein
    Barbut, Denise
    Stolzenberg, Ethan
    Zasloff, Michael
    [J]. JOURNAL OF PARKINSONS DISEASE, 2019, 9 : S313 - S322
  • [2] Beerten J, 2012, CURR TOP MED CHEM, V12, P2470
  • [3] Amyloid formation modulates the biological activity of a bacterial protein
    Bieler, S
    Estrada, L
    Lagos, R
    Baeza, M
    Castilla, J
    Soto, C
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (29) : 26880 - 26885
  • [4] Antimicrobial peptides: Pore formers or metabolic inhibitors in bacteria?
    Brogden, KA
    [J]. NATURE REVIEWS MICROBIOLOGY, 2005, 3 (03) : 238 - 250
  • [5] The endotoxin hypothesis of neurodegeneration
    Brown, Guy C.
    [J]. JOURNAL OF NEUROINFLAMMATION, 2019, 16 (01) : 180
  • [6] Human α-Defensin 6: A Small Peptide That Self-Assembles and Protects the Host by Entangling Microbes
    Chairatana, Phoom
    Nolan, Elizabeth M.
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2017, 50 (04) : 960 - 967
  • [7] Protein Misfolding, Amyloid Formation, and Human Disease: A Summary of Progress Over the Last Decade
    Chiti, Fabrizio
    Dobson, Christopher M.
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, VOL 86, 2017, 86 : 27 - 68
  • [8] Alternatives to antibiotics-a pipeline portfolio review
    Czaplewski, Lloyd
    Bax, Richard
    Clokie, Martha
    Dawson, Mike
    Fairhead, Heather
    Fischetti, Vincent A.
    Foster, Simon
    Gilmore, Brendan F.
    Hancock, Robert E. W.
    Harper, David
    Henderson, Ian R.
    Hilpert, Kai
    Jones, Brian V.
    Kadioglu, Aras
    Knowles, David
    Olafsdottir, Sigridur
    Payne, David
    Projan, Steve
    Shaunak, Sunil
    Silverman, Jared
    Thomas, Christopher M.
    Trust, Trevor J.
    Warn, Peter
    Rex, John H.
    [J]. LANCET INFECTIOUS DISEASES, 2016, 16 (02) : 239 - 251
  • [9] de Groot NS, 2012, METHODS MOL BIOL, V819, P199, DOI 10.1007/978-1-61779-465-0_14
  • [10] The Amyloid Phenomenon and Its Links with Human Disease
    Dobson, Christopher M.
    [J]. COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2017, 9 (06):