Towards understanding nuclear pore complex architecture and dynamics in the age of integrative structural analysis
Determining the functional architecture of the nuclear pore complex, that remains only partially understood, requires bridging across different length scales. Recent technological advances in quantitative and cross-linking mass spectrometry, super-resolution fluorescence microscopy and electron micr...
Ausführliche Beschreibung
Autor*in: |
Hurt, Ed - 1955- [verfasserIn] Beck, Martin - 1977- [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
15 May 2015 |
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Anmerkung: |
Gesehen am 03.06.2020 |
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Umfang: |
8 |
Übergeordnetes Werk: |
Enthalten in: Current opinion in cell biology - Amsterdam [u.a.] : Elsevier, 1989, 34(2015), Seite 31-38 |
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Übergeordnetes Werk: |
volume:34 ; year:2015 ; pages:31-38 ; extent:8 |
Links: |
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DOI / URN: |
10.1016/j.ceb.2015.04.009 |
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Katalog-ID: |
1699274290 |
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520 | |a Determining the functional architecture of the nuclear pore complex, that remains only partially understood, requires bridging across different length scales. Recent technological advances in quantitative and cross-linking mass spectrometry, super-resolution fluorescence microscopy and electron microscopy have enormously accelerated the integration of different types of data into coherent structural models. Moreover, high-resolution structural analysis of nucleoporins and their in vitro reconstitution into complexes is now facilitated by the use of thermostable orthologs. In this review we highlight how the application of such technologies has led to novel insights into nuclear pore architecture and to a paradigm shift. Today nuclear pores are not anymore seen as static facilitators of nucleocytoplasmic transport but ensembles of multiple overlaying functional states that are involved in various cellular processes. | ||
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15 May 2015 |
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2015 |
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10.1016/j.ceb.2015.04.009 doi (DE-627)1699274290 (DE-599)KXP1699274290 (OCoLC)1341327379 DE-627 ger DE-627 rda eng Hurt, Ed 1955- verfasserin (DE-588)11021952X (DE-627)729291863 (DE-576)373308574 aut Towards understanding nuclear pore complex architecture and dynamics in the age of integrative structural analysis Ed Hurt and Martin Beck 15 May 2015 8 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Gesehen am 03.06.2020 Determining the functional architecture of the nuclear pore complex, that remains only partially understood, requires bridging across different length scales. Recent technological advances in quantitative and cross-linking mass spectrometry, super-resolution fluorescence microscopy and electron microscopy have enormously accelerated the integration of different types of data into coherent structural models. Moreover, high-resolution structural analysis of nucleoporins and their in vitro reconstitution into complexes is now facilitated by the use of thermostable orthologs. In this review we highlight how the application of such technologies has led to novel insights into nuclear pore architecture and to a paradigm shift. Today nuclear pores are not anymore seen as static facilitators of nucleocytoplasmic transport but ensembles of multiple overlaying functional states that are involved in various cellular processes. Beck, Martin 1977- verfasserin (DE-588)131458647 (DE-627)509456634 (DE-576)29849101X aut Enthalten in Current opinion in cell biology Amsterdam [u.a.] : Elsevier, 1989 34(2015), Seite 31-38 Online-Ressource (DE-627)320507688 (DE-600)2013029-6 (DE-576)094113610 1879-0410 nnns volume:34 year:2015 pages:31-38 extent:8 https://doi.org/10.1016/j.ceb.2015.04.009 Verlag Resolving-System lizenzpflichtig Volltext http://www.sciencedirect.com/science/article/pii/S0955067415000496 Verlag lizenzpflichtig Volltext GBV_USEFLAG_U GBV_ILN_2013 ISIL_DE-16-250 SYSFLAG_1 GBV_KXP GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_211 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2098 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 AR 34 2015 31-38 8 2013 01 DE-16-250 3681716250 00 --%%-- --%%-- --%%-- --%%-- l01 03-06-20 2013 01 DE-16-250 00 s hd2015 2013 01 DE-16-250 01 s (DE-627)1410508463 wissenschaftlicher Artikel (Zeitschrift) 2013 01 DE-16-250 02 s per_2 2013 01 DE-16-250 03 s s_8 2013 01 DE-16-250 04 p (DE-627)1443445231 Hurt, Ed 2013 01 DE-16-250 04 k (DE-627)1416733434 Biochemiezentrum der Universität Heidelberg (BZH) 2013 01 DE-16-250 04 k (DE-627)1416737693 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 01 DE-16-250 04 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 04 s pos_1 2013 01 DE-16-250 05 p (DE-627)1577895916 Beck, Martin 2013 01 DE-16-250 05 k (DE-627)1416822720 Extern 2013 01 DE-16-250 05 k (DE-627)1416737693 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 01 DE-16-250 05 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 05 s pos_2 |
spelling |
10.1016/j.ceb.2015.04.009 doi (DE-627)1699274290 (DE-599)KXP1699274290 (OCoLC)1341327379 DE-627 ger DE-627 rda eng Hurt, Ed 1955- verfasserin (DE-588)11021952X (DE-627)729291863 (DE-576)373308574 aut Towards understanding nuclear pore complex architecture and dynamics in the age of integrative structural analysis Ed Hurt and Martin Beck 15 May 2015 8 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Gesehen am 03.06.2020 Determining the functional architecture of the nuclear pore complex, that remains only partially understood, requires bridging across different length scales. Recent technological advances in quantitative and cross-linking mass spectrometry, super-resolution fluorescence microscopy and electron microscopy have enormously accelerated the integration of different types of data into coherent structural models. Moreover, high-resolution structural analysis of nucleoporins and their in vitro reconstitution into complexes is now facilitated by the use of thermostable orthologs. In this review we highlight how the application of such technologies has led to novel insights into nuclear pore architecture and to a paradigm shift. Today nuclear pores are not anymore seen as static facilitators of nucleocytoplasmic transport but ensembles of multiple overlaying functional states that are involved in various cellular processes. Beck, Martin 1977- verfasserin (DE-588)131458647 (DE-627)509456634 (DE-576)29849101X aut Enthalten in Current opinion in cell biology Amsterdam [u.a.] : Elsevier, 1989 34(2015), Seite 31-38 Online-Ressource (DE-627)320507688 (DE-600)2013029-6 (DE-576)094113610 1879-0410 nnns volume:34 year:2015 pages:31-38 extent:8 https://doi.org/10.1016/j.ceb.2015.04.009 Verlag Resolving-System lizenzpflichtig Volltext http://www.sciencedirect.com/science/article/pii/S0955067415000496 Verlag lizenzpflichtig Volltext GBV_USEFLAG_U GBV_ILN_2013 ISIL_DE-16-250 SYSFLAG_1 GBV_KXP GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_211 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2098 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 AR 34 2015 31-38 8 2013 01 DE-16-250 3681716250 00 --%%-- --%%-- --%%-- --%%-- l01 03-06-20 2013 01 DE-16-250 00 s hd2015 2013 01 DE-16-250 01 s (DE-627)1410508463 wissenschaftlicher Artikel (Zeitschrift) 2013 01 DE-16-250 02 s per_2 2013 01 DE-16-250 03 s s_8 2013 01 DE-16-250 04 p (DE-627)1443445231 Hurt, Ed 2013 01 DE-16-250 04 k (DE-627)1416733434 Biochemiezentrum der Universität Heidelberg (BZH) 2013 01 DE-16-250 04 k (DE-627)1416737693 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 01 DE-16-250 04 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 04 s pos_1 2013 01 DE-16-250 05 p (DE-627)1577895916 Beck, Martin 2013 01 DE-16-250 05 k (DE-627)1416822720 Extern 2013 01 DE-16-250 05 k (DE-627)1416737693 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 01 DE-16-250 05 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 05 s pos_2 |
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10.1016/j.ceb.2015.04.009 doi (DE-627)1699274290 (DE-599)KXP1699274290 (OCoLC)1341327379 DE-627 ger DE-627 rda eng Hurt, Ed 1955- verfasserin (DE-588)11021952X (DE-627)729291863 (DE-576)373308574 aut Towards understanding nuclear pore complex architecture and dynamics in the age of integrative structural analysis Ed Hurt and Martin Beck 15 May 2015 8 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Gesehen am 03.06.2020 Determining the functional architecture of the nuclear pore complex, that remains only partially understood, requires bridging across different length scales. Recent technological advances in quantitative and cross-linking mass spectrometry, super-resolution fluorescence microscopy and electron microscopy have enormously accelerated the integration of different types of data into coherent structural models. Moreover, high-resolution structural analysis of nucleoporins and their in vitro reconstitution into complexes is now facilitated by the use of thermostable orthologs. In this review we highlight how the application of such technologies has led to novel insights into nuclear pore architecture and to a paradigm shift. Today nuclear pores are not anymore seen as static facilitators of nucleocytoplasmic transport but ensembles of multiple overlaying functional states that are involved in various cellular processes. Beck, Martin 1977- verfasserin (DE-588)131458647 (DE-627)509456634 (DE-576)29849101X aut Enthalten in Current opinion in cell biology Amsterdam [u.a.] : Elsevier, 1989 34(2015), Seite 31-38 Online-Ressource (DE-627)320507688 (DE-600)2013029-6 (DE-576)094113610 1879-0410 nnns volume:34 year:2015 pages:31-38 extent:8 https://doi.org/10.1016/j.ceb.2015.04.009 Verlag Resolving-System lizenzpflichtig Volltext http://www.sciencedirect.com/science/article/pii/S0955067415000496 Verlag lizenzpflichtig Volltext GBV_USEFLAG_U GBV_ILN_2013 ISIL_DE-16-250 SYSFLAG_1 GBV_KXP GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_211 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2098 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 AR 34 2015 31-38 8 2013 01 DE-16-250 3681716250 00 --%%-- --%%-- --%%-- --%%-- l01 03-06-20 2013 01 DE-16-250 00 s hd2015 2013 01 DE-16-250 01 s (DE-627)1410508463 wissenschaftlicher Artikel (Zeitschrift) 2013 01 DE-16-250 02 s per_2 2013 01 DE-16-250 03 s s_8 2013 01 DE-16-250 04 p (DE-627)1443445231 Hurt, Ed 2013 01 DE-16-250 04 k (DE-627)1416733434 Biochemiezentrum der Universität Heidelberg (BZH) 2013 01 DE-16-250 04 k (DE-627)1416737693 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 01 DE-16-250 04 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 04 s pos_1 2013 01 DE-16-250 05 p (DE-627)1577895916 Beck, Martin 2013 01 DE-16-250 05 k (DE-627)1416822720 Extern 2013 01 DE-16-250 05 k (DE-627)1416737693 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 01 DE-16-250 05 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 05 s pos_2 |
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10.1016/j.ceb.2015.04.009 doi (DE-627)1699274290 (DE-599)KXP1699274290 (OCoLC)1341327379 DE-627 ger DE-627 rda eng Hurt, Ed 1955- verfasserin (DE-588)11021952X (DE-627)729291863 (DE-576)373308574 aut Towards understanding nuclear pore complex architecture and dynamics in the age of integrative structural analysis Ed Hurt and Martin Beck 15 May 2015 8 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Gesehen am 03.06.2020 Determining the functional architecture of the nuclear pore complex, that remains only partially understood, requires bridging across different length scales. Recent technological advances in quantitative and cross-linking mass spectrometry, super-resolution fluorescence microscopy and electron microscopy have enormously accelerated the integration of different types of data into coherent structural models. Moreover, high-resolution structural analysis of nucleoporins and their in vitro reconstitution into complexes is now facilitated by the use of thermostable orthologs. In this review we highlight how the application of such technologies has led to novel insights into nuclear pore architecture and to a paradigm shift. Today nuclear pores are not anymore seen as static facilitators of nucleocytoplasmic transport but ensembles of multiple overlaying functional states that are involved in various cellular processes. Beck, Martin 1977- verfasserin (DE-588)131458647 (DE-627)509456634 (DE-576)29849101X aut Enthalten in Current opinion in cell biology Amsterdam [u.a.] : Elsevier, 1989 34(2015), Seite 31-38 Online-Ressource (DE-627)320507688 (DE-600)2013029-6 (DE-576)094113610 1879-0410 nnns volume:34 year:2015 pages:31-38 extent:8 https://doi.org/10.1016/j.ceb.2015.04.009 Verlag Resolving-System lizenzpflichtig Volltext http://www.sciencedirect.com/science/article/pii/S0955067415000496 Verlag lizenzpflichtig Volltext GBV_USEFLAG_U GBV_ILN_2013 ISIL_DE-16-250 SYSFLAG_1 GBV_KXP GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_211 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2098 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 AR 34 2015 31-38 8 2013 01 DE-16-250 3681716250 00 --%%-- --%%-- --%%-- --%%-- l01 03-06-20 2013 01 DE-16-250 00 s hd2015 2013 01 DE-16-250 01 s (DE-627)1410508463 wissenschaftlicher Artikel (Zeitschrift) 2013 01 DE-16-250 02 s per_2 2013 01 DE-16-250 03 s s_8 2013 01 DE-16-250 04 p (DE-627)1443445231 Hurt, Ed 2013 01 DE-16-250 04 k (DE-627)1416733434 Biochemiezentrum der Universität Heidelberg (BZH) 2013 01 DE-16-250 04 k (DE-627)1416737693 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 01 DE-16-250 04 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 04 s pos_1 2013 01 DE-16-250 05 p (DE-627)1577895916 Beck, Martin 2013 01 DE-16-250 05 k (DE-627)1416822720 Extern 2013 01 DE-16-250 05 k (DE-627)1416737693 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 01 DE-16-250 05 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 05 s pos_2 |
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2013 01 DE-16-250 00 s hd2015 2013 01 DE-16-250 01 s (DE-627)1410508463 wissenschaftlicher Artikel (Zeitschrift) 2013 01 DE-16-250 02 s per_2 2013 01 DE-16-250 03 s s_8 2013 01 DE-16-250 04 p (DE-627)1443445231 Hurt, Ed 2013 01 DE-16-250 04 k (DE-627)1416733434 Biochemiezentrum der Universität Heidelberg (BZH) 2013 01 DE-16-250 04 k (DE-627)1416737693 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 01 DE-16-250 04 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 04 s pos_1 2013 01 DE-16-250 05 p (DE-627)1577895916 Beck, Martin 2013 01 DE-16-250 05 k (DE-627)1416822720 Extern 2013 01 DE-16-250 05 k (DE-627)1416737693 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 01 DE-16-250 05 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 05 s pos_2 Towards understanding nuclear pore complex architecture and dynamics in the age of integrative structural analysis Ed Hurt and Martin Beck |
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2013 hd2015 2013 wissenschaftlicher Artikel (Zeitschrift) 2013 per_2 2013 s_8 2013 Hurt, Ed 2013 Biochemiezentrum der Universität Heidelberg (BZH) 2013 Exzellenzcluster Zelluläre Netzwerke (EXCCN) 2013 Verfasser 2013 pos_1 2013 Beck, Martin 2013 Extern 2013 pos_2 |
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towards understanding nuclear pore complex architecture and dynamics in the age of integrative structural analysis |
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Towards understanding nuclear pore complex architecture and dynamics in the age of integrative structural analysis |
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Determining the functional architecture of the nuclear pore complex, that remains only partially understood, requires bridging across different length scales. Recent technological advances in quantitative and cross-linking mass spectrometry, super-resolution fluorescence microscopy and electron microscopy have enormously accelerated the integration of different types of data into coherent structural models. Moreover, high-resolution structural analysis of nucleoporins and their in vitro reconstitution into complexes is now facilitated by the use of thermostable orthologs. In this review we highlight how the application of such technologies has led to novel insights into nuclear pore architecture and to a paradigm shift. Today nuclear pores are not anymore seen as static facilitators of nucleocytoplasmic transport but ensembles of multiple overlaying functional states that are involved in various cellular processes. Gesehen am 03.06.2020 |
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Determining the functional architecture of the nuclear pore complex, that remains only partially understood, requires bridging across different length scales. Recent technological advances in quantitative and cross-linking mass spectrometry, super-resolution fluorescence microscopy and electron microscopy have enormously accelerated the integration of different types of data into coherent structural models. Moreover, high-resolution structural analysis of nucleoporins and their in vitro reconstitution into complexes is now facilitated by the use of thermostable orthologs. In this review we highlight how the application of such technologies has led to novel insights into nuclear pore architecture and to a paradigm shift. Today nuclear pores are not anymore seen as static facilitators of nucleocytoplasmic transport but ensembles of multiple overlaying functional states that are involved in various cellular processes. Gesehen am 03.06.2020 |
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Determining the functional architecture of the nuclear pore complex, that remains only partially understood, requires bridging across different length scales. Recent technological advances in quantitative and cross-linking mass spectrometry, super-resolution fluorescence microscopy and electron microscopy have enormously accelerated the integration of different types of data into coherent structural models. Moreover, high-resolution structural analysis of nucleoporins and their in vitro reconstitution into complexes is now facilitated by the use of thermostable orthologs. In this review we highlight how the application of such technologies has led to novel insights into nuclear pore architecture and to a paradigm shift. Today nuclear pores are not anymore seen as static facilitators of nucleocytoplasmic transport but ensembles of multiple overlaying functional states that are involved in various cellular processes. Gesehen am 03.06.2020 |
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Towards understanding nuclear pore complex architecture and dynamics in the age of integrative structural analysis |
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