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          <dc:title>Negative Interfacial
Tension Driven by Intrinsic Molecular
Disorder</dc:title>
          <dc:creator>Chuan Tang (1938364)</dc:creator>
          <dc:creator>Yifan Huang (1371063)</dc:creator>
          <dc:creator>Chun-Lai Ren (8678247)</dc:creator>
          <dc:creator>Qiyun Tang (124659)</dc:creator>
          <dc:creator>Yu-Qiang Ma (8678250)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Physical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>δγ ∼ −&lt;</dc:subject>
          <dc:subject>law size distribution</dc:subject>
          <dc:subject>law cluster distributions</dc:subject>
          <dc:subject>intrinsic molecular disorder</dc:subject>
          <dc:subject>general physicochemical mechanism</dc:subject>
          <dc:subject>diverse experimental observations</dc:subject>
          <dc:subject>intrinsically disordered proteins</dc:subject>
          <dc:subject>effective interfacial tension</dc:subject>
          <dc:subject>conserved density field</dc:subject>
          <dc:subject>two fields χ</dc:subject>
          <dc:subject>ϵ &lt;/ sub</dc:subject>
          <dc:subject>effective parameters</dc:subject>
          <dc:subject>disordered biomolecules</dc:subject>
          <dc:subject>junction field</dc:subject>
          <dc:subject>field theories</dc:subject>
          <dc:subject>&gt;&lt; sub</dc:subject>
          <dc:subject>work reveals</dc:subject>
          <dc:subject>random copolymers</dc:subject>
          <dc:subject>polydisperse assemblies</dc:subject>
          <dc:subject>oriented framework</dc:subject>
          <dc:subject>numerical calculations</dc:subject>
          <dc:subject>negative values</dc:subject>
          <dc:subject>grained simulations</dc:subject>
          <dc:subject>fundamental challenge</dc:subject>
          <dc:subject>explicitly links</dc:subject>
          <dc:subject>conventional mean</dc:subject>
          <dc:description>Intrinsically disordered molecular systems, such as random
copolymers
and intrinsically disordered proteins, exhibit scale-invariant, power-law
cluster distributions that cannot be explained by conventional mean-field
theories. A fundamental challenge is to understand how sequence randomness,
which cannot be averaged into effective parameters, drives the formation
of such polydisperse assemblies. Using a minimal coupled field theory
that explicitly links a conserved density field to a nonconserved
“junction” field representing stochastic binding site
density, we show that the attraction between two fields χ, together
with the fluctuations in the junction field &lt;i&gt;T&lt;/i&gt;&lt;sub&gt;ϵ&lt;/sub&gt;, renormalizes the effective interfacial tension to
negative values: Δγ ∼ −&lt;i&gt;T&lt;/i&gt;&lt;sub&gt;ϵ&lt;/sub&gt;χ&lt;sup&gt;2&lt;/sup&gt;. This negative interfacial
tension suppresses coalescence and stabilizes a scale-invariant ensemble
of clusters with a power-law size distribution, as confirmed by both
numerical calculations and coarse-grained simulations of sequence-disordered
biomolecules, and are consistent with diverse experimental observations.
Our work reveals a general physicochemical mechanism by which intrinsic
molecular disorder and fluctuations jointly govern phase separation
in systems with built-in randomness, providing a unifying, chemistry-oriented
framework for understanding and engineering heterogeneous soft matter
systems.</dc:description>
          <dc:date>2026-09-25T00:00:00Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Media</dc:type>
          <dc:identifier>10.1021/jacs.6c10169.s004</dc:identifier>
          <dc:relation>https://figshare.com/articles/media/Negative_Interfacial_Tension_Driven_by_Intrinsic_Molecular_Disorder/33993977</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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