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Structure-function relationships of the soluble form of the antiaging protein Klotho have therapeutic implications for managing kidney disease.
Zhong, Xiaotian; Jagarlapudi, Srinath; Weng, Yan; Ly, Mellisa; Rouse, Jason C; McClure, Kim; Ishino, Tetsuya; Zhang, Yan; Sousa, Eric; Cohen, Justin; Tzvetkova, Boriana; Cote, Kaffa; Scarcelli, John J; Johnson, Keith; Palandra, Joe; Apgar, James R; Yaddanapudi, Suma; Gonzalez-Villalobos, Romer A; Opsahl, Alan C; Lam, Khetemenee; Yao, Qing; Duan, Weili; Sievers, Annette; Zhou, Jing; Ferguson, Darren; D'Antona, Aaron; Zollner, Richard; Zhu, Hongli L; Kriz, Ron; Lin, Laura; Clerin, Valerie.
Afiliación
  • Zhong X; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139. Electronic address: Xiaotian.Zhong@pfizer.com.
  • Jagarlapudi S; Internal Medicine, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Weng Y; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Ly M; Analytical Research and Development, Biotherapeutics Pharmaceutical Sciences, Pfizer Inc., Andover, Massachusetts 01810.
  • Rouse JC; Analytical Research and Development, Biotherapeutics Pharmaceutical Sciences, Pfizer Inc., Andover, Massachusetts 01810.
  • McClure K; Internal Medicine, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Ishino T; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Zhang Y; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Sousa E; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Cohen J; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Tzvetkova B; Analytical Research and Development, Biotherapeutics Pharmaceutical Sciences, Pfizer Inc., Andover, Massachusetts 01810.
  • Cote K; Analytical Research and Development, Biotherapeutics Pharmaceutical Sciences, Pfizer Inc., Andover, Massachusetts 01810.
  • Scarcelli JJ; Cell Line Development, Biotherapeutics Pharmaceutical Sciences, Pfizer Inc., Andover, Massachusetts 01810.
  • Johnson K; Analytical Research and Development, Biotherapeutics Pharmaceutical Sciences, Pfizer Inc., Andover, Massachusetts 01810.
  • Palandra J; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Apgar JR; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Yaddanapudi S; Internal Medicine, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Gonzalez-Villalobos RA; Internal Medicine, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Opsahl AC; Internal Medicine, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Lam K; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Yao Q; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Duan W; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Sievers A; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Zhou J; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Ferguson D; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • D'Antona A; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Zollner R; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Zhu HL; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Kriz R; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Lin L; BioMedicine Design, Pfizer Worldwide Research, Cambridge, Massachusetts 02139.
  • Clerin V; Internal Medicine, Pfizer Worldwide Research, Cambridge, Massachusetts 02139. Electronic address: Valerie.Clerin@pfizer.com.
J Biol Chem ; 295(10): 3115-3133, 2020 03 06.
Article en En | MEDLINE | ID: mdl-32005658
The fortuitously discovered antiaging membrane protein αKlotho (Klotho) is highly expressed in the kidney, and deletion of the Klotho gene in mice causes a phenotype strikingly similar to that of chronic kidney disease (CKD). Klotho functions as a co-receptor for fibroblast growth factor 23 (FGF23) signaling, whereas its shed extracellular domain, soluble Klotho (sKlotho), carrying glycosidase activity, is a humoral factor that regulates renal health. Low sKlotho in CKD is associated with disease progression, and sKlotho supplementation has emerged as a potential therapeutic strategy for managing CKD. Here, we explored the structure-function relationship and post-translational modifications of sKlotho variants to guide the future design of sKlotho-based therapeutics. Chinese hamster ovary (CHO)- and human embryonic kidney (HEK)-derived WT sKlotho proteins had varied activities in FGF23 co-receptor and ß-glucuronidase assays in vitro and distinct properties in vivo Sialidase treatment of heavily sialylated CHO-sKlotho increased its co-receptor activity 3-fold, yet it remained less active than hyposialylated HEK-sKlotho. MS and glycopeptide-mapping analyses revealed that HEK-sKlotho is uniquely modified with an unusual N-glycan structure consisting of N,N'-di-N-acetyllactose diamine at multiple N-linked sites, one of which at Asn-126 was adjacent to a putative GalNAc transfer motif. Site-directed mutagenesis and structural modeling analyses directly implicated N-glycans in Klotho's protein folding and function. Moreover, the introduction of two catalytic glutamate residues conserved across glycosidases into sKlotho enhanced its glucuronidase activity but decreased its FGF23 co-receptor activity, suggesting that these two functions might be structurally divergent. These findings open up opportunities for rational engineering of pharmacologically enhanced sKlotho therapeutics for managing kidney disease.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Insuficiencia Renal Crónica / Glucuronidasa Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Biol Chem Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Insuficiencia Renal Crónica / Glucuronidasa Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Biol Chem Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos