Literature DB >> 16969692

Controlling protein compartmentalization to overcome disease.

James R Davis1, Mudit Kakar, Carol S Lim.   

Abstract

Over the past decade, considerable progress has been made to improve our understanding of the intracellular transport of proteins. Mechanisms of nuclear import and export involving classical receptors have been studied. Signal sequences required for directing a protein molecule to a specific cellular compartment have been defined. Knowledge of subcellular trafficking of proteins has also increased our understanding of diseases caused due to mislocalization of proteins. A specific protein on deviating from its native cellular compartment may result in disease due to loss of its normal functioning and aberrant activity in the "wrong" compartment. Mislocalization of proteins results in diseases that range from metabolic disorders to cancer. In this review we discuss some of the diseases caused due to mislocalization. We further focus on application of nucleocytoplasmic transport to drug delivery. Various rationales to treat diseases by exploiting intracellular transport machinery have been proposed. Although the pathways for intracellular movement of proteins have been defined, these have not been adequately utilized for management of diseases involving mislocalized proteins. This review stresses the need for designing drug delivery systems utilizing these mechanisms as this area is least exploited but offers great potential.

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Year:  2006        PMID: 16969692     DOI: 10.1007/s11095-006-9133-z

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  120 in total

1.  BARD1 regulates BRCA1 apoptotic function by a mechanism involving nuclear retention.

Authors:  Megan Fabbro; Stefan Schuechner; Wendy W Y Au; Beric R Henderson
Journal:  Exp Cell Res       Date:  2004-08-15       Impact factor: 3.905

2.  A Rae1-containing ribonucleoprotein complex is required for mitotic spindle assembly.

Authors:  Michael D Blower; Maxence Nachury; Rebecca Heald; Karsten Weis
Journal:  Cell       Date:  2005-04-22       Impact factor: 41.582

3.  Evidence for distinct substrate specificities of importin alpha family members in nuclear protein import.

Authors:  M Köhler; C Speck; M Christiansen; F R Bischoff; S Prehn; H Haller; D Görlich; E Hartmann
Journal:  Mol Cell Biol       Date:  1999-11       Impact factor: 4.272

4.  BARD1 induces BRCA1 intranuclear foci formation by increasing RING-dependent BRCA1 nuclear import and inhibiting BRCA1 nuclear export.

Authors:  Megan Fabbro; Jose A Rodriguez; Richard Baer; Beric R Henderson
Journal:  J Biol Chem       Date:  2002-03-29       Impact factor: 5.157

5.  Major binding sites for the nuclear import receptor are the internal nucleoporin Nup153 and the adjacent nuclear filament protein Tpr.

Authors:  S Shah; S Tugendreich; D Forbes
Journal:  J Cell Biol       Date:  1998-04-06       Impact factor: 10.539

6.  Ca2+-dependent nuclear export mediated by calreticulin.

Authors:  James M Holaska; Ben E Black; Fraydoon Rastinejad; Bryce M Paschal
Journal:  Mol Cell Biol       Date:  2002-09       Impact factor: 4.272

7.  Calreticulin Is a receptor for nuclear export.

Authors:  J M Holaska; B E Black; D C Love; J A Hanover; J Leszyk; B M Paschal
Journal:  J Cell Biol       Date:  2001-01-08       Impact factor: 10.539

8.  Ran-binding protein 3 is a cofactor for Crm1-mediated nuclear protein export.

Authors:  M E Lindsay; J M Holaska; K Welch; B M Paschal; I G Macara
Journal:  J Cell Biol       Date:  2001-06-25       Impact factor: 10.539

9.  A nuclear export signal in Kap95p is required for both recycling the import factor and interaction with the nucleoporin GLFG repeat regions of Nup116p and Nup100p.

Authors:  M K Iovine; S R Wente
Journal:  J Cell Biol       Date:  1997-05-19       Impact factor: 10.539

10.  The GLFG repetitive region of the nucleoporin Nup116p interacts with Kap95p, an essential yeast nuclear import factor.

Authors:  M K Iovine; J L Watkins; S R Wente
Journal:  J Cell Biol       Date:  1995-12       Impact factor: 10.539

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  27 in total

1.  The nuclear translocation assay for intracellular protein-protein interactions and its application to the Bcr coiled-coil domain.

Authors:  Andrew S Dixon; Carol S Lim
Journal:  Biotechniques       Date:  2010-07       Impact factor: 1.993

2.  Optimizing the protein switch: altering nuclear import and export signals, and ligand binding domain.

Authors:  Mudit Kakar; James R Davis; Steve E Kern; Carol S Lim
Journal:  J Control Release       Date:  2007-05-03       Impact factor: 9.776

3.  Signal sequences for targeting of gene therapy products to subcellular compartments: the role of CRM1 in nucleocytoplasmic shuttling of the protein switch.

Authors:  Mudit Kakar; Amy B Cadwallader; James R Davis; Carol S Lim
Journal:  Pharm Res       Date:  2007-06-13       Impact factor: 4.200

4.  Determining the distribution of probes between different subcellular locations through automated unmixing of subcellular patterns.

Authors:  Tao Peng; Ghislain M C Bonamy; Estelle Glory-Afshar; Daniel R Rines; Sumit K Chanda; Robert F Murphy
Journal:  Proc Natl Acad Sci U S A       Date:  2010-02-01       Impact factor: 11.205

5.  Direct induction of apoptosis using an optimal mitochondrially targeted p53.

Authors:  Mohanad Mossalam; Karina J Matissek; Abood Okal; Jonathan E Constance; Carol S Lim
Journal:  Mol Pharm       Date:  2012-03-28       Impact factor: 4.939

Review 6.  Nuclear export of proteins and drug resistance in cancer.

Authors:  Joel G Turner; Jana Dawson; Daniel M Sullivan
Journal:  Biochem Pharmacol       Date:  2011-12-20       Impact factor: 5.858

Review 7.  The androgen receptor and its use in biological assays: looking toward effect-based testing and its applications.

Authors:  Amy B Cadwallader; Carol S Lim; Douglas E Rollins; Francesco Botrè
Journal:  J Anal Toxicol       Date:  2011-11       Impact factor: 3.367

8.  Ran-binding protein 3 phosphorylation links the Ras and PI3-kinase pathways to nucleocytoplasmic transport.

Authors:  Sang-Oh Yoon; Sejeong Shin; Yuzhen Liu; Bryan A Ballif; Michele S Woo; Steven P Gygi; John Blenis
Journal:  Mol Cell       Date:  2008-02-15       Impact factor: 17.970

9.  Human multiple myeloma cells are sensitized to topoisomerase II inhibitors by CRM1 inhibition.

Authors:  Joel G Turner; Douglas C Marchion; Jana L Dawson; Michael F Emmons; Lori A Hazlehurst; Peter Washausen; Daniel M Sullivan
Journal:  Cancer Res       Date:  2009-08-18       Impact factor: 12.701

10.  Controlling subcellular localization to alter function: Sending oncogenic Bcr-Abl to the nucleus causes apoptosis.

Authors:  Andrew S Dixon; Mudit Kakar; Korbinian M H Schneider; Jonathan E Constance; Blake C Paullin; Carol S Lim
Journal:  J Control Release       Date:  2009-07-01       Impact factor: 9.776

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