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Brush Effects on DNA Chips: Thermodynamics, Kinetics, and Design Guidelines
In biology experiments, oligonucleotide microarrays are contacted with a solution of long nucleic acid targets. The hybridized probes thus carry long tails. When the surface density of the oligonucleotide probes is high enough, the progress of hybridization gives rise to a polyelectrolyte brush due...
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Published in: | Biophysical journal 2005-08, Vol.89 (2), p.796-811 |
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description | In biology experiments, oligonucleotide microarrays are contacted with a solution of long nucleic acid targets. The hybridized probes thus carry long tails. When the surface density of the oligonucleotide probes is high enough, the progress of hybridization gives rise to a polyelectrolyte brush due to mutual crowding of the nucleic acid tails. The free-energy penalty associated with the brush modifies both the hybridization isotherms and the rate equations: the attainable hybridization is lowered significantly as is the hybridization rate. When the equilibrium hybridization fraction,
x
eq, is low, the hybridization follows a Langmuir type isotherm,
x
eq/(1
-
x
eq)
=
c
t
K where
c
t is the target concentration and
K is the equilibrium constant.
K is smaller than its bulk value by a factor (
n/
N)
2/5 due to wall effects where
n and
N denote the number of bases in the probe and the target. At higher
x
eq, when the brush is formed, the leading correction is
x
eq
/
(
1
−
x
eq
)
=
c
t
K
exp
−
c
o
n
s
t
'
x
eq
2
/
3
−
x
B
2
/
3
where
x
B corresponds to the onset of the brush regime. The denaturation rate constant in the two regimes is identical. However, the hybridization rate constant in the brush regime is lower, the leading correction being
exp
−
c
o
n
s
t
'
x
2
/
3
−
x
B
2
/
3 |
doi_str_mv | 10.1529/biophysj.105.063479 |
format | article |
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x
eq, is low, the hybridization follows a Langmuir type isotherm,
x
eq/(1
-
x
eq)
=
c
t
K where
c
t is the target concentration and
K is the equilibrium constant.
K is smaller than its bulk value by a factor (
n/
N)
2/5 due to wall effects where
n and
N denote the number of bases in the probe and the target. At higher
x
eq, when the brush is formed, the leading correction is
x
eq
/
(
1
−
x
eq
)
=
c
t
K
exp
−
c
o
n
s
t
'
x
eq
2
/
3
−
x
B
2
/
3
where
x
B corresponds to the onset of the brush regime. The denaturation rate constant in the two regimes is identical. However, the hybridization rate constant in the brush regime is lower, the leading correction being
exp
−
c
o
n
s
t
'
x
2
/
3
−
x
B
2
/
3</description><identifier>ISSN: 0006-3495</identifier><identifier>EISSN: 1542-0086</identifier><identifier>DOI: 10.1529/biophysj.105.063479</identifier><identifier>PMID: 15908581</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biophysical Theory and Modeling ; Biotechnology ; Computer Simulation ; Computer-Aided Design ; Deoxyribonucleic acid ; DNA ; DNA - analysis ; DNA - chemistry ; DNA Probes - analysis ; DNA Probes - chemistry ; Equipment Design - methods ; Equipment Failure Analysis ; Gene expression ; Hybridization ; In Situ Hybridization - methods ; Kinetics ; Life Sciences ; Models, Chemical ; Nucleic Acid Denaturation ; Oligonucleotide Array Sequence Analysis - instrumentation ; Oligonucleotide Array Sequence Analysis - methods ; Thermodynamics</subject><ispartof>Biophysical journal, 2005-08, Vol.89 (2), p.796-811</ispartof><rights>2005 The Biophysical Society</rights><rights>Copyright Biophysical Society Aug 2005</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2005, Biophysical Society 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c584t-c2bb12f22b8017e98059619455a3058ed1e9afbe605a51c16e74875172e07b8b3</citedby><cites>FETCH-LOGICAL-c584t-c2bb12f22b8017e98059619455a3058ed1e9afbe605a51c16e74875172e07b8b3</cites><orcidid>0000-0001-7643-4305</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1366630/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1366630/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15908581$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://cea.hal.science/cea-02531570$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Halperin, A.</creatorcontrib><creatorcontrib>Buhot, A.</creatorcontrib><creatorcontrib>Zhulina, E.B.</creatorcontrib><title>Brush Effects on DNA Chips: Thermodynamics, Kinetics, and Design Guidelines</title><title>Biophysical journal</title><addtitle>Biophys J</addtitle><description>In biology experiments, oligonucleotide microarrays are contacted with a solution of long nucleic acid targets. The hybridized probes thus carry long tails. When the surface density of the oligonucleotide probes is high enough, the progress of hybridization gives rise to a polyelectrolyte brush due to mutual crowding of the nucleic acid tails. The free-energy penalty associated with the brush modifies both the hybridization isotherms and the rate equations: the attainable hybridization is lowered significantly as is the hybridization rate. When the equilibrium hybridization fraction,
x
eq, is low, the hybridization follows a Langmuir type isotherm,
x
eq/(1
-
x
eq)
=
c
t
K where
c
t is the target concentration and
K is the equilibrium constant.
K is smaller than its bulk value by a factor (
n/
N)
2/5 due to wall effects where
n and
N denote the number of bases in the probe and the target. At higher
x
eq, when the brush is formed, the leading correction is
x
eq
/
(
1
−
x
eq
)
=
c
t
K
exp
−
c
o
n
s
t
'
x
eq
2
/
3
−
x
B
2
/
3
where
x
B corresponds to the onset of the brush regime. The denaturation rate constant in the two regimes is identical. However, the hybridization rate constant in the brush regime is lower, the leading correction being
exp
−
c
o
n
s
t
'
x
2
/
3
−
x
B
2
/
3</description><subject>Biophysical Theory and Modeling</subject><subject>Biotechnology</subject><subject>Computer Simulation</subject><subject>Computer-Aided Design</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA - analysis</subject><subject>DNA - chemistry</subject><subject>DNA Probes - analysis</subject><subject>DNA Probes - chemistry</subject><subject>Equipment Design - methods</subject><subject>Equipment Failure Analysis</subject><subject>Gene expression</subject><subject>Hybridization</subject><subject>In Situ Hybridization - methods</subject><subject>Kinetics</subject><subject>Life Sciences</subject><subject>Models, Chemical</subject><subject>Nucleic Acid Denaturation</subject><subject>Oligonucleotide Array Sequence Analysis - instrumentation</subject><subject>Oligonucleotide Array Sequence Analysis - methods</subject><subject>Thermodynamics</subject><issn>0006-3495</issn><issn>1542-0086</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp9kV-L1DAUxYMo7rj6CQQpPgiCHW_SJk0FhXF23ZUd9GV9Dml6u83QJmPSDsy3t2PHf_vgU0Lu75xD7iHkOYUl5ax8W1m_aw9xu6TAlyCyvCgfkAXlOUsBpHhIFgAg0iwv-Rl5EuMWgDIO9DE5o7wEySVdkJuPYYxtctk0aIaYeJdcfFkl69bu4rvktsXQ-_rgdG9NfJPcWIfDz5t2dXKB0d655Gq0NXbTJD4ljxrdRXx2Os_Jt0-Xt-vrdPP16vN6tUkNl_mQGlZVlDWMVRJogaUEXgpa5pzrDLjEmmKpmwoFcM2poQKLXBacFgyhqGSVnZMPs-9urHqsDboh6E7tgu11OCivrfp34myr7vxe0UwIkcFk8Ho2aO_JrlcbZVArYDyjvIA9ndhXp7Dgv48YB9XbaLDrtEM_RiUkSJnlbAJf3gO3fgxuWoRiRy8u5NEtmyETfIwBm9_xFNSxVfWr1emBq7nVSfXi7w__0ZxqnID3M4DT2vcWg4rGojNY2zD1qmpv_xvwAzoisu0</recordid><startdate>20050801</startdate><enddate>20050801</enddate><creator>Halperin, A.</creator><creator>Buhot, A.</creator><creator>Zhulina, E.B.</creator><general>Elsevier Inc</general><general>Biophysical Society</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7643-4305</orcidid></search><sort><creationdate>20050801</creationdate><title>Brush Effects on DNA Chips: Thermodynamics, Kinetics, and Design Guidelines</title><author>Halperin, A. ; Buhot, A. ; Zhulina, E.B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c584t-c2bb12f22b8017e98059619455a3058ed1e9afbe605a51c16e74875172e07b8b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Biophysical Theory and Modeling</topic><topic>Biotechnology</topic><topic>Computer Simulation</topic><topic>Computer-Aided Design</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA - analysis</topic><topic>DNA - chemistry</topic><topic>DNA Probes - analysis</topic><topic>DNA Probes - chemistry</topic><topic>Equipment Design - methods</topic><topic>Equipment Failure Analysis</topic><topic>Gene expression</topic><topic>Hybridization</topic><topic>In Situ Hybridization - methods</topic><topic>Kinetics</topic><topic>Life Sciences</topic><topic>Models, Chemical</topic><topic>Nucleic Acid Denaturation</topic><topic>Oligonucleotide Array Sequence Analysis - instrumentation</topic><topic>Oligonucleotide Array Sequence Analysis - methods</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Halperin, A.</creatorcontrib><creatorcontrib>Buhot, A.</creatorcontrib><creatorcontrib>Zhulina, E.B.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Research Library (ProQuest)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biophysical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Halperin, A.</au><au>Buhot, A.</au><au>Zhulina, E.B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brush Effects on DNA Chips: Thermodynamics, Kinetics, and Design Guidelines</atitle><jtitle>Biophysical journal</jtitle><addtitle>Biophys J</addtitle><date>2005-08-01</date><risdate>2005</risdate><volume>89</volume><issue>2</issue><spage>796</spage><epage>811</epage><pages>796-811</pages><issn>0006-3495</issn><eissn>1542-0086</eissn><abstract>In biology experiments, oligonucleotide microarrays are contacted with a solution of long nucleic acid targets. The hybridized probes thus carry long tails. When the surface density of the oligonucleotide probes is high enough, the progress of hybridization gives rise to a polyelectrolyte brush due to mutual crowding of the nucleic acid tails. The free-energy penalty associated with the brush modifies both the hybridization isotherms and the rate equations: the attainable hybridization is lowered significantly as is the hybridization rate. When the equilibrium hybridization fraction,
x
eq, is low, the hybridization follows a Langmuir type isotherm,
x
eq/(1
-
x
eq)
=
c
t
K where
c
t is the target concentration and
K is the equilibrium constant.
K is smaller than its bulk value by a factor (
n/
N)
2/5 due to wall effects where
n and
N denote the number of bases in the probe and the target. At higher
x
eq, when the brush is formed, the leading correction is
x
eq
/
(
1
−
x
eq
)
=
c
t
K
exp
−
c
o
n
s
t
'
x
eq
2
/
3
−
x
B
2
/
3
where
x
B corresponds to the onset of the brush regime. The denaturation rate constant in the two regimes is identical. However, the hybridization rate constant in the brush regime is lower, the leading correction being
exp
−
c
o
n
s
t
'
x
2
/
3
−
x
B
2
/
3</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15908581</pmid><doi>10.1529/biophysj.105.063479</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0001-7643-4305</orcidid><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | PubMed Central |
subjects | Biophysical Theory and Modeling Biotechnology Computer Simulation Computer-Aided Design Deoxyribonucleic acid DNA DNA - analysis DNA - chemistry DNA Probes - analysis DNA Probes - chemistry Equipment Design - methods Equipment Failure Analysis Gene expression Hybridization In Situ Hybridization - methods Kinetics Life Sciences Models, Chemical Nucleic Acid Denaturation Oligonucleotide Array Sequence Analysis - instrumentation Oligonucleotide Array Sequence Analysis - methods Thermodynamics |
title | Brush Effects on DNA Chips: Thermodynamics, Kinetics, and Design Guidelines |
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