{"id":1603,"date":"2020-01-28T19:02:24","date_gmt":"2020-01-28T18:02:24","guid":{"rendered":"https:\/\/www.nanoworld.com\/blog\/?p=1603"},"modified":"2023-04-18T12:59:23","modified_gmt":"2023-04-18T11:59:23","slug":"the-free-energy-landscape-of-retroviral-integration","status":"publish","type":"post","link":"https:\/\/www.nanoworld.com\/blog\/the-free-energy-landscape-of-retroviral-integration\/","title":{"rendered":"The free energy landscape of retroviral integration"},"content":{"rendered":"\n<p>Retroviral\nintegration, the process of covalently inserting viral DNA into the host\ngenome, is a point of no return in the replication cycle. Yet, strand transfer\nis intrinsically iso-energetic and it is not clear how efficient integration\ncan be achieved.*<\/p>\n\n\n\n<p>In the\narticle \u201c<em>The free energy landscape of retroviral integration<\/em>\u201d published\nin Nature Communications Willem Vanderlinden, Tine Brouns, Philipp U. Walker,\nPauline J. Kolbeck, Lukas F. Milles, Wolfgang Ott, Philipp C. Nickels, Zeger\nDebyser and Jan Lipfert use biochemical assays, atomic force microscopy (AFM),\nand multiplexed single-molecule magnetic tweezers (MT) to study tetrameric\nprototype foamy virus (PFV) strand-transfer dynamics.*<\/p>\n\n\n\n<p>Their finding that PFV intasomes employ auxiliary-binding sites for modulating the barriers to integration raises the question how the topology of higher-order intasomes governs integration of pathogenic retroviruses, most notably HIV. The single-molecule assays developed in this work are expected to be particularly useful to further unravel the complexity of this important class of molecular machines.* <\/p>\n\n\n\n<p>The AFM images were recorded in amplitude modulation mode under ambient conditions and by using NanoWorld high resolution <a rel=\"noreferrer noopener\" aria-label=\"SuperSharpSilicon (opens in a new tab)\" href=\"https:\/\/youtu.be\/qcS-d6qJFrQ\" target=\"_blank\">SuperSharpSilicon<\/a>\u2122 <a rel=\"noreferrer noopener\" aria-label=\"SSS-NCH  (opens in a new tab)\" href=\"https:\/\/www.nanoworld.com\/pointprobe-super-sharp-silicon-tapping-mode-afm-tip-sss-nch\" target=\"_blank\">SSS-NCH <\/a>cantilevers ( resonance frequency \u2248300\u2009kHz; typical end-radius 2\u2009nm; half-cone angle &lt;10\u2009deg). Typical scans were recorded at 1\u20133\u2009Hz line frequency, with optimized feedback parameters and at 512\u2009\u00d7\u2009512 pixels.*<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"1200\" height=\"732\" src=\"https:\/\/dhipgo7nn2tea.cloudfront.net\/wp-content\/uploads\/2020\/01\/28174505\/Figure-2-e_f_g-from-%E2%80%9CThe-free-energy-landscape-of-retroviral-integration%E2%80%9D-by-Willem-Vanderlinden-et-al-2019-Nat-Commun-10-4738-2019.jpg\" alt=\"Figure 2 e, f and g from \u201cThe free energy landscape of retroviral integration\u201d by Willem Vanderlinden et al. \n(please refer to the full article for the complete figure 2  https:\/\/rdcu.be\/b0R63 ) :\n  e Atomic Force Microscopy image of intasomes incubated briefly (2\u2009min) with supercoiled plasmid DNA, depicting a branched complex as found in ~50% of early complexes.\n  f  Atomic Force Microscopy image of a bridging complex that dominates (~80%) the population of complexes at longer (&gt;45\u2009min) incubation. \n g  Atomic Force Microscopy image of a gel-purified STC \" class=\"wp-image-1607\" srcset=\"https:\/\/dhipgo7nn2tea.cloudfront.net\/wp-content\/uploads\/2020\/01\/28174505\/Figure-2-e_f_g-from-%E2%80%9CThe-free-energy-landscape-of-retroviral-integration%E2%80%9D-by-Willem-Vanderlinden-et-al-2019-Nat-Commun-10-4738-2019.jpg 1200w, https:\/\/dhipgo7nn2tea.cloudfront.net\/wp-content\/uploads\/2020\/01\/28174505\/Figure-2-e_f_g-from-%E2%80%9CThe-free-energy-landscape-of-retroviral-integration%E2%80%9D-by-Willem-Vanderlinden-et-al-2019-Nat-Commun-10-4738-2019-300x183.jpg 300w, https:\/\/dhipgo7nn2tea.cloudfront.net\/wp-content\/uploads\/2020\/01\/28174505\/Figure-2-e_f_g-from-%E2%80%9CThe-free-energy-landscape-of-retroviral-integration%E2%80%9D-by-Willem-Vanderlinden-et-al-2019-Nat-Commun-10-4738-2019-1024x625.jpg 1024w, https:\/\/dhipgo7nn2tea.cloudfront.net\/wp-content\/uploads\/2020\/01\/28174505\/Figure-2-e_f_g-from-%E2%80%9CThe-free-energy-landscape-of-retroviral-integration%E2%80%9D-by-Willem-Vanderlinden-et-al-2019-Nat-Commun-10-4738-2019-768x468.jpg 768w, https:\/\/dhipgo7nn2tea.cloudfront.net\/wp-content\/uploads\/2020\/01\/28174505\/Figure-2-e_f_g-from-%E2%80%9CThe-free-energy-landscape-of-retroviral-integration%E2%80%9D-by-Willem-Vanderlinden-et-al-2019-Nat-Commun-10-4738-2019-800x488.jpg 800w\" sizes=\"auto, (max-width: 1200px) 100vw, 1200px\" \/><figcaption>Figure 2 e, f and g from \u201cThe free energy landscape of retroviral integration\u201d by Willem Vanderlinden et al. <br>(please refer to the full article for the complete figure 2  <a href=\"https:\/\/rdcu.be\/b0R63\" target=\"_blank\" rel=\"noreferrer noopener\" aria-label=\" (opens in a new tab)\">https:\/\/rdcu.be\/b0R63<\/a> ) :<br> \u00a0e AFM image of intasomes incubated briefly (2\u2009min) with supercoiled plasmid DNA, depicting a branched complex as found in ~50% of early complexes.<br> \u00a0f AFM image of a bridging complex that dominates (~80%) the population of complexes at longer (>45\u2009min) incubation. <br> g AFM image of a gel-purified STC <\/figcaption><\/figure>\n\n\n\n<p> *Willem Vanderlinden, Tine Brouns, Philipp U. Walker, Pauline J. Kolbeck, Lukas F. Milles, Wolfgang Ott, Philipp C. Nickels, Zeger Debyser, Jan Lipfert<br><strong>The free energy landscape of retroviral integration<\/strong><br> Nature Communications volume 10, Article number: 4738 (2019)<br> DOI: https:\/\/doi.org\/10.1038\/s41467-019-12649-w <\/p>\n\n\n\n<p> Please follow this external link to read the full article: <a href=\"https:\/\/rdcu.be\/b0R63\" target=\"_blank\" rel=\"noreferrer noopener\" aria-label=\"https:\/\/rdcu.be\/b0R63 (opens in a new tab)\">https:\/\/rdcu.be\/b0R63<\/a><\/p>\n\n\n\n<p> Open Access The article \u201c<em>The free energy landscape of retroviral integration<\/em>\u201c by Willem Vanderlinden, Tine Brouns, Philipp U. Walker, Pauline J. Kolbeck, Lukas F. Milles, Wolfgang Ott, Philipp C. Nickels, Zeger Debyser and Jan Lipfert is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article\u2019s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article\u2019s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit <a href=\"http:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noreferrer noopener\" aria-label=\"http:\/\/creativecommons.org\/licenses\/by\/4.0\/ (opens in a new tab)\">http:\/\/creativecommons.org\/licenses\/by\/4.0\/<\/a>. <\/p>\n","protected":false},"excerpt":{"rendered":"<p>Retroviral integration, the process of covalently inserting viral DNA into the host genome, is a point of no return in the replication cycle. Yet, strand transfer is intrinsically iso-energetic and it is not clear how efficient integration can be achieved.* In the article \u201cThe free energy landscape of retroviral integration\u201d published in Nature Communications Willem &hellip; <a href=\"https:\/\/www.nanoworld.com\/blog\/the-free-energy-landscape-of-retroviral-integration\/\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\" >The free energy landscape of retroviral integration<\/span><\/a><\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[3],"tags":[62,10,66,65,228,17,93,48,96,287,27,47,250,290,86,288,16,137,13,12,241,229,286,28,289],"class_list":{"0":"post-1603","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"hentry","6":"category-news","7":"tag-afm-probes","8":"tag-afm-tips","9":"tag-afm","12":"tag-atomic-force-microscopy","13":"tag-biology","14":"tag-biology-afm-probes","15":"tag-biophysics","16":"tag-enzyme-mechanisms","17":"tag-high-resolution-imaging","18":"tag-life-science-afm-probes","19":"tag-molecular-biology","20":"tag-molecular-machines","21":"tag-nanoscale-biophysics","22":"tag-retroviral-integration","23":"tag-scanning-probe-microscopy","24":"tag-single-molecule-biophysics","25":"tag-spm-probes","26":"tag-spm-tips","27":"tag-spm","29":"tag-sss-nch","30":"tag-supersharp-silicon","31":"tag-viral-dna"},"_links":{"self":[{"href":"https:\/\/www.nanoworld.com\/blog\/wp-json\/wp\/v2\/posts\/1603","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.nanoworld.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.nanoworld.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.nanoworld.com\/blog\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.nanoworld.com\/blog\/wp-json\/wp\/v2\/comments?post=1603"}],"version-history":[{"count":9,"href":"https:\/\/www.nanoworld.com\/blog\/wp-json\/wp\/v2\/posts\/1603\/revisions"}],"predecessor-version":[{"id":1613,"href":"https:\/\/www.nanoworld.com\/blog\/wp-json\/wp\/v2\/posts\/1603\/revisions\/1613"}],"wp:attachment":[{"href":"https:\/\/www.nanoworld.com\/blog\/wp-json\/wp\/v2\/media?parent=1603"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.nanoworld.com\/blog\/wp-json\/wp\/v2\/categories?post=1603"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.nanoworld.com\/blog\/wp-json\/wp\/v2\/tags?post=1603"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}