Literature DB >> 33659495

Expression and Purification of Recombinant Skd3 (Human ClpB) Protein and Tobacco Etch Virus (TEV) Protease from Escherichia coli.

Ryan R Cupo1,2, James Shorter1,2.   

Abstract

Skd3 (encoded by human CLPB) is a mitochondrial AAA+ protein comprised of an N-terminal ankyrin-repeat domain and a C-terminal HCLR-clade nucleotide-binding domain. The function of Skd3 has long remained unknown due to challenges in purifying the protein to high quality and near homogeneity. Recently we described Skd3 as a human mitochondrial protein disaggregase that solubilizes proteins in the mitochondrial intermembrane space. This protocol overcomes the challenges associated with purifying Skd3 and allows for in depth in vitro study of Skd3 activity. Tobacco etch virus (TEV) protease is required in the purification of Skd3. Thus, we also describe how to purify high quality TEV protease for use in the purification of Skd3, other purification protocols, and in vitro assays requiring TEV protease.
Copyright © The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  CLPB; Chaperone; Protein aggregation; Protein disaggregase; Skd3; TEV

Year:  2020        PMID: 33659495      PMCID: PMC7842574          DOI: 10.21769/BioProtoc.3858

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  8 in total

1.  Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia.

Authors:  Ayca Kiykim; Wojciech Garncarz; Elif Karakoc-Aydiner; Ahmet Ozen; Ertugrul Kiykim; Gozde Yesil; Kaan Boztug; Safa Baris
Journal:  Clin Immunol       Date:  2016-02-23       Impact factor: 3.969

2.  CLPB (caseinolytic peptidase B homolog), the first mitochondrial protein refoldase associated with human disease.

Authors:  Dagmara Mróz; Hubert Wyszkowski; Tomasz Szablewski; Katarzyna Zawieracz; Rafał Dutkiewicz; Katarzyna Bury; Saskia B Wortmann; Ron A Wevers; Szymon Ziętkiewicz
Journal:  Biochim Biophys Acta Gen Subj       Date:  2020-01-07       Impact factor: 3.770

3.  RNA Binding Antagonizes Neurotoxic Phase Transitions of TDP-43.

Authors:  Jacob R Mann; Amanda M Gleixner; Jocelyn C Mauna; Edward Gomes; Michael R DeChellis-Marks; Patrick G Needham; Katie E Copley; Bryan Hurtle; Bede Portz; Noah J Pyles; Lin Guo; Christopher B Calder; Zachary P Wills; Udai B Pandey; Julia K Kofler; Jeffrey L Brodsky; Amantha Thathiah; James Shorter; Christopher J Donnelly
Journal:  Neuron       Date:  2019-02-27       Impact factor: 17.173

4.  Bi-allelic CLPB mutations cause cataract, renal cysts, nephrocalcinosis and 3-methylglutaconic aciduria, a novel disorder of mitochondrial protein disaggregation.

Authors:  Marta Kanabus; Rojeen Shahni; José W Saldanha; Elaine Murphy; Vincent Plagnol; William Van't Hoff; Simon Heales; Shamima Rahman
Journal:  J Inherit Metab Dis       Date:  2015-01-18       Impact factor: 4.982

5.  CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder.

Authors:  Saskia B Wortmann; Szymon Ziętkiewicz; Maria Kousi; Radek Szklarczyk; Tobias B Haack; Søren W Gersting; Ania C Muntau; Aleksandar Rakovic; G Herma Renkema; Richard J Rodenburg; Tim M Strom; Thomas Meitinger; M Estela Rubio-Gozalbo; Elzbieta Chrusciel; Felix Distelmaier; Christelle Golzio; Joop H Jansen; Clara van Karnebeek; Yolanda Lillquist; Thomas Lücke; Katrin Õunap; Riina Zordania; Joy Yaplito-Lee; Hans van Bokhoven; Johannes N Spelbrink; Frédéric M Vaz; Mia Pras-Raves; Rafal Ploski; Ewa Pronicka; Christine Klein; Michel A A P Willemsen; Arjan P M de Brouwer; Holger Prokisch; Nicholas Katsanis; Ron A Wevers
Journal:  Am J Hum Genet       Date:  2015-01-15       Impact factor: 11.025

6.  CLPB variants associated with autosomal-recessive mitochondrial disorder with cataract, neutropenia, epilepsy, and methylglutaconic aciduria.

Authors:  Carol Saunders; Laurie Smith; Flemming Wibrand; Kirstine Ravn; Peter Bross; Isabelle Thiffault; Mette Christensen; Andrea Atherton; Emily Farrow; Neil Miller; Stephen F Kingsmore; Elsebet Ostergaard
Journal:  Am J Hum Genet       Date:  2015-01-15       Impact factor: 11.025

7.  Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria.

Authors:  José-Mario Capo-Chichi; Sarah Boissel; Edna Brustein; Sarah Pickles; Catherine Fallet-Bianco; Christina Nassif; Lysanne Patry; Sylvia Dobrzeniecka; Meijiang Liao; Damian Labuda; Mark E Samuels; Fadi F Hamdan; Christine Vande Velde; Guy A Rouleau; Pierre Drapeau; Jacques L Michaud
Journal:  J Med Genet       Date:  2015-02-03       Impact factor: 6.318

8.  Skd3 (human ClpB) is a potent mitochondrial protein disaggregase that is inactivated by 3-methylglutaconic aciduria-linked mutations.

Authors:  Ryan R Cupo; James Shorter
Journal:  Elife       Date:  2020-06-23       Impact factor: 8.140

  8 in total
  4 in total

1.  Human mitochondrial AAA+ ATPase SKD3/CLPB assembles into nucleotide-stabilized dodecamers.

Authors:  Zachary Spaulding; Indhujah Thevarajan; Lynn G Schrag; Lejla Zubcevic; Anna Zolkiewska; Michal Zolkiewski
Journal:  Biochem Biophys Res Commun       Date:  2022-02-25       Impact factor: 3.575

2.  Unique structural features govern the activity of a human mitochondrial AAA+ disaggregase, Skd3.

Authors:  Ryan R Cupo; Alexandrea N Rizo; Gabriel A Braun; Eric Tse; Edward Chuang; Kushol Gupta; Daniel R Southworth; James Shorter
Journal:  Cell Rep       Date:  2022-09-27       Impact factor: 9.995

3.  Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy.

Authors:  Hong Joo Kim; Payam Mohassel; Sandra Donkervoort; Lin Guo; Kevin O'Donovan; Maura Coughlin; Xaviere Lornage; Nicola Foulds; Simon R Hammans; A Reghan Foley; Charlotte M Fare; Alice F Ford; Masashi Ogasawara; Aki Sato; Aritoshi Iida; Pinki Munot; Gautam Ambegaonkar; Rahul Phadke; Dominic G O'Donovan; Rebecca Buchert; Mona Grimmel; Ana Töpf; Irina T Zaharieva; Lauren Brady; Ying Hu; Thomas E Lloyd; Andrea Klein; Maja Steinlin; Alice Kuster; Sandra Mercier; Pascale Marcorelles; Yann Péréon; Emmanuelle Fleurence; Adnan Manzur; Sarah Ennis; Rosanna Upstill-Goddard; Luca Bello; Cinzia Bertolin; Elena Pegoraro; Leonardo Salviati; Courtney E French; Andriy Shatillo; F Lucy Raymond; Tobias B Haack; Susana Quijano-Roy; Johann Böhm; Isabelle Nelson; Tanya Stojkovic; Teresinha Evangelista; Volker Straub; Norma B Romero; Jocelyn Laporte; Francesco Muntoni; Ichizo Nishino; Mark A Tarnopolsky; James Shorter; Carsten G Bönnemann; J Paul Taylor
Journal:  Nat Commun       Date:  2022-04-28       Impact factor: 17.694

4.  Heterozygous variants of CLPB are a cause of severe congenital neutropenia.

Authors:  Julia T Warren; Ryan R Cupo; Peeradol Wattanasirakul; David H Spencer; Adam E Locke; Vahagn Makaryan; Audrey Anna Bolyard; Merideth L Kelley; Natalie L Kingston; James Shorter; Christine Bellanné-Chantelot; Jean Donadieu; David C Dale; Daniel C Link
Journal:  Blood       Date:  2022-02-03       Impact factor: 25.476

  4 in total

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