Literature DB >> 8921841

Candidacidal activity of human salivary histatin recombinant variants produced by site-directed mutagenesis.

J Driscoll1, C Duan, Y Zuo, T Xu, R Troxler, F G Oppenheim.   

Abstract

Histatin 5 (Hst5) is a 24-amino acid (aa) member of the Hst family that is found in human salivary secretions and exhibits candidacidal activity. Hst5 contains a 13-aa region that alone is capable of killing fungal pathogens and is referred to as the functional domain. To investigate the role of specific aa located within the functional domain, the pRSET bacterial expression system was used to produce recombinant Hst5 (re-Hst5) and several re-variants that were generated by site-directed mutagenesis. The vector pRSETC expresses genes of interest as fusion proteins attached to the carboxy end of an N-terminal His6 tag that binds to nickel (Ni2+). The re-variants were generated using the polymerase chain reaction (PCR) and had Gly substituted for either the His, Glu or Lys/Arg within the functional domain. PCR products that encoded either the wild-type or variant forms of re-Hst5 were inserted into pRSETC and produced as fusion proteins which were affinity purified from cell lysates by Ni(2+)-Sepharose chromatography. Fusion proteins were digested with CNBr and re-Hsts were purified by reversed-phase high performance liquid chromatography (RP-HPLC). Re-Hsts were tested in bioassays to measure the ability to kill both Candida albicans (C. albicans) blastoconidia and spheroplasts which were generated by removal of the cell wall. In both assays, re-Hst5 displayed dose-dependent candidacidal activity that was nearly identical to that of native Hst5 purified from human salivary secretions. Re-Hst5 variants with either Glu or Lys/Arg substitutions demonstrated significantly lower candidacidal activity in both assays, while the variant with His mutated showed essentially no activity at physiological concentrations. These results indicate that acidic and basic aa within the functional domain contribute to candidacidal activity and that the His are essential for candidacidal activity. Additionally, since C. albicans spheroplasts were also susceptible to Hsts, the cell wall is not an essential component in the Hst mechanism of candidacidal action.

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Year:  1996        PMID: 8921841     DOI: 10.1016/0378-1119(96)00265-x

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  11 in total

1.  Anticandida activity is retained in P-113, a 12-amino-acid fragment of histatin 5.

Authors:  D M Rothstein; P Spacciapoli; L T Tran; T Xu; F D Roberts; M Dalla Serra; D K Buxton; F G Oppenheim; P Friden
Journal:  Antimicrob Agents Chemother       Date:  2001-05       Impact factor: 5.191

Review 2.  How does it kill?: understanding the candidacidal mechanism of salivary histatin 5.

Authors:  Sumant Puri; Mira Edgerton
Journal:  Eukaryot Cell       Date:  2014-06-20

3.  Engineering improved variants of the antifungal peptide histatin 5 with reduced susceptibility to Candida albicans secreted aspartic proteases and enhanced antimicrobial potency.

Authors:  Svetlana P Ikonomova; Parisa Moghaddam-Taaheri; Mary Ann Jabra-Rizk; Yan Wang; Amy J Karlsson
Journal:  FEBS J       Date:  2017-11-29       Impact factor: 5.542

4.  Histatin 3-mediated killing of Candida albicans: effect of extracellular salt concentration on binding and internalization.

Authors:  Y Xu; I Ambudkar; H Yamagishi; W Swaim; T J Walsh; B C O'Connell
Journal:  Antimicrob Agents Chemother       Date:  1999-09       Impact factor: 5.191

5.  The P-113 fragment of histatin 5 requires a specific peptide sequence for intracellular translocation in Candida albicans, which is independent of cell wall binding.

Authors:  Woong Sik Jang; Xuewei Serene Li; Jianing N Sun; Mira Edgerton
Journal:  Antimicrob Agents Chemother       Date:  2007-11-12       Impact factor: 5.191

6.  The Antimicrobial Peptides P-113Du and P-113Tri Function against Candida albicans.

Authors:  Guan-Yu Lin; Hsueh-Fen Chen; Yao-Peng Xue; Ying-Chieh Yeh; Chia-Lu Chen; Ming-Sun Liu; Wen-Chi Cheng; Chung-Yu Lan
Journal:  Antimicrob Agents Chemother       Date:  2016-09-23       Impact factor: 5.191

7.  Effects of histatin 5 modifications on antifungal activity and kinetics of proteolysis.

Authors:  Svetlana P Ikonomova; Parisa Moghaddam-Taaheri; Yan Wang; Mary T Doolin; Kimberly M Stroka; Bernhard Hube; Amy J Karlsson
Journal:  Protein Sci       Date:  2019-11-20       Impact factor: 6.725

8.  Anti-candidal activity of genetically engineered histatin variants with multiple functional domains.

Authors:  Frank G Oppenheim; Eva J Helmerhorst; Urs Lendenmann; Gwynneth D Offner
Journal:  PLoS One       Date:  2012-12-12       Impact factor: 3.240

9.  The antimicrobial peptide histatin-5 causes a spatially restricted disruption on the Candida albicans surface, allowing rapid entry of the peptide into the cytoplasm.

Authors:  A Brian Mochon; Haoping Liu
Journal:  PLoS Pathog       Date:  2008-10-31       Impact factor: 6.823

10.  Novel mitochondrial complex I-inhibiting peptides restrain NADH dehydrogenase activity.

Authors:  Yao-Peng Xue; Mou-Chieh Kao; Chung-Yu Lan
Journal:  Sci Rep       Date:  2019-09-23       Impact factor: 4.379

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