<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kang D</submitter><funding>Natural Sciences and Engineering Research Council of Canada</funding><funding>Nanyang Technological University</funding><funding>Basic Energy Sciences</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><pagination>13346-13352</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8968159</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>37(45)</volume><pubmed_abstract>Using a surface forces apparatus (SFA), we have studied the nanomechanical behavior of short single-stranded and partially and fully double-stranded DNA molecules attached via one end to a self-assembled monolayer on a gold surface. Our results confirm the previously proposed "mushroom-like" polymer structure for surface-attached, single-stranded DNA at low packing density and a "brush-like" structure for the same construct at higher density. At low density we observe a transition to "rigid rod" behavior upon addition of DNA complementary to the surface-attached single strand as the fraction of molecules that are double-stranded increases, with a concomitant increase in the SFA-observed thickness of the monolayer and the characteristic length of the observed repulsive forces. At higher densities, in contrast, this transition is effectively eliminated, presumably because the single-stranded state is already extended in its "brush" state. Taken together, these studies offer insights into the structure and physics of surface-attached short DNAs, providing new guidance for the rational design of DNA-modified functional surfaces.</pubmed_abstract><journal>Langmuir : the ACS journal of surfaces and colloids</journal><pubmed_title>Nanometer-Scale Force Profiles of Short Single- and Double-Stranded DNA Molecules on a Gold Surface Measured Using a Surface Forces Apparatus.</pubmed_title><pmcid>PMC8968159</pmcid><funding_grant_id>RO1GM118560</funding_grant_id><funding_grant_id>M4082049.070</funding_grant_id><funding_grant_id>R01 GM118560</funding_grant_id><pubmed_authors>Israelachvili J</pubmed_authors><pubmed_authors>Plaxco KW</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Kang D</pubmed_authors><pubmed_authors>Zeng H</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Tirrell M</pubmed_authors><pubmed_authors>Xia F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nanometer-Scale Force Profiles of Short Single- and Double-Stranded DNA Molecules on a Gold Surface Measured Using a Surface Forces Apparatus.</name><description>Using a surface forces apparatus (SFA), we have studied the nanomechanical behavior of short single-stranded and partially and fully double-stranded DNA molecules attached via one end to a self-assembled monolayer on a gold surface. Our results confirm the previously proposed "mushroom-like" polymer structure for surface-attached, single-stranded DNA at low packing density and a "brush-like" structure for the same construct at higher density. At low density we observe a transition to "rigid rod" behavior upon addition of DNA complementary to the surface-attached single strand as the fraction of molecules that are double-stranded increases, with a concomitant increase in the SFA-observed thickness of the monolayer and the characteristic length of the observed repulsive forces. At higher densities, in contrast, this transition is effectively eliminated, presumably because the single-stranded state is already extended in its "brush" state. Taken together, these studies offer insights into the structure and physics of surface-attached short DNAs, providing new guidance for the rational design of DNA-modified functional surfaces.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2025-04-27T01:08:52.436Z</modification><creation>2025-04-06T18:07:22.423Z</creation></dates><accession>S-EPMC8968159</accession><cross_references><pubmed>34730362</pubmed><doi>10.1021/acs.langmuir.1c01966</doi></cross_references></HashMap>